J. Epplen

J. Epplen, C. Maser-Gluth, G. Dekomien, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Helicobacter pylori infection: CagA-specific antibodies are associated with clinical outcome, but not with HLA-class II polymorphisms of the host.

J. Epplen, S. Suerbaum, J. Crabtree, 2003, International journal of medical microbiology : IJMM.

The organization of the evolutionarily conserved GATA/GACA repeats in the mouse genome

J. Epplen, Sher Ali, R. Schäfer, 2004, Chromosoma.

Replication Analysis of a Putative Susceptibility Locus (EGI) for Idiopathic Generalized Epilepsy on Chromosome 8q24

J. Epplen, G. Bauer, H. Schulz, 1998, Epilepsia.

Dissecting (CAC)5/(GTG)5 multilocus fingerprints from man into individual locus-specific, hypervariable components.

K. Grzeschik, J. Epplen, H. Zischler, 1992, Genomics.

Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2)

M. Vorgerd, J. Epplen, M. Meins, 2006, BMC Medical Genetics.

MAN1B1 Mutation Leads to a Recognizable Phenotype: A Case Report and Future Prospects

R. Abou Jamra, A. Reis, J. Epplen, 2015, Molecular Syndromology.

Severe Guillain–Barré syndrome associated with chromosome 17p11.2‐12 duplication

J. Epplen, R. Meyer, C. Münch, 2008, Muscle & nerve.

Transmission distortion of the mutant alleles in spinocerebellar ataxia

L. Schöls, H. Przuntek, O. Riess, 1997, Human Genetics.

Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish families.

K. Fenger, O. Riess, J. Epplen, 1993, Human molecular genetics.

Variation in genes encoding eosinophil granule proteins in atopic dermatitis patients from Germany

J. Epplen, S. Hoffjan, Q. Parwez, 2008, Journal of Negative Results in BioMedicine.

Dinucleotide repeat polymorphism in the human IL1A gene.

J. Epplen, E. Albert, P. Nurnberg, 1994, Human molecular genetics.

Dinucleotide repeat polymorphism in the IL2 and IL5RA genes.

P. Nürnberg, J. Epplen, M. Nagy, 1994, Human molecular genetics.

Characterization of a human chromosome 4 flow-sorted cosmid library.

L. Deaven, O. Riess, J. Epplen, 1994, Cytogenetics and cell genetics.

A promotor polymorphism in the Interleukin 11 gene is associated with chronic obstructive pulmonary disease

J. Epplen, G. Rohde, G. Schultze-Werninghaus, 2004, Electrophoresis.

Complex genetics of Wegener granulomatosis.

J. Epplen, W. Gross, P. Jagiello, 2005, Autoimmunity reviews.

Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF

J. Epplen, W. M. Gerding, C. Neusch, 2009, Neuromuscular Disorders.

Analysis of the C19orf12 and WDR45 genes in patients with neurodegeneration with brain iron accumulation

J. Epplen, K. Cremer, G. Dekomien, 2015, Journal of Neurological Sciences.

Reproductive success of monogamous and polygynous pied flycatchers (Ficedula hypoleuca)

W. Winkel, J. Epplen, T. Lubjuhn, 2000, Behavioral Ecology and Sociobiology.

PATERNAL GENETIC EFFECTS ON OFFSPRING FITNESS ARE CONTEXT DEPENDENT WITHIN THE EXTRAPAIR MATING SYSTEM OF A SOCIALLY MONOGAMOUS PASSERINE

F. Schurr, T. Schmoll, V. Dietrich, 2005, Evolution; international journal of organic evolution.

Female influences on pair formation, reproduction and male stress responses in a monogamous cavy (Galea monasteriensis)

J. Epplen, N. Sachser, M. Hennessy, 2008, Hormones and Behavior.

Low frequency of extra-pair paternity in Common Gulls (Larus canus) as revealed by DNA fingerprinting

J. Epplen, T. Lubjuhn, K. P. Sauer, 1998, Journal für Ornithologie.

Fingerprinting plant genomes with oligonucleotide probes specific for simple repetitive DNA sequences

P. Nürnberg, B. Beyermann, J. Epplen, 1992, Theoretical and Applied Genetics.

Truly hypervariable DNA fingerprints due to exceptionally high mutation rates

J. Epplen, T. Lubjuhn, P. Quillfeldt, 2002, Electrophoresis.

Genetic Monogamy in Wilson's Storm-Petrel

T. Schmoll, J. Epplen, T. Lubjuhn, 2001 .

Low probe concentration can cause problems in multilocus DNA fingerprinting (cautionary notes III)

J. Epplen, T. Lubjuhn, T. Gerken, 2000, Electrophoresis.

High Frequency of Extra-Pair Paternity in the Coal Tit

J. Epplen, T. Lubjuhn, J. Brün, 1999 .

Multilocus DNA fingerprints in the plant Cynoglossum officinale L. and their use in the estimation of selfing

J. Epplen, K. Vrieling, P. Saumitou-Laprade, 1997 .

Tumor Genome Screening by Multilocus DNA Fingerprints as Obtained by Simple Repetitive Oligonucleotide Probes

P. Nürnberg, J. Epplen, S. Bock, 1993 .

Coamplification of simple repetitive DNA fingerprint fragments and the EGFR gene in human gliomas

D. Kinzel, P. Nürnberg, J. Epplen, 1991, Genes, chromosomes & cancer.

Stain analysis using oligonucleotide probes specific for simple repetitive DNA sequences.

L. Roewer, P. Nürnberg, J. Epplen, 1990, Forensic science international.

Non-radioactive oligonucleotide fingerprinting in the gel.

J. Epplen, H. Zischler, R. Schäfer, 1989, Nucleic acids research.

Clustered GATA repeats (Bkm sequences) on the human Y chromosome

J. Schmidtke, J. Epplen, S. Jakubiczka, 1986, Human Genetics.

Evaluation of the gamma-synuclein gene in German Parkinson's disease patients.

R. Krüger, L. Schöls, H. Przuntek, 2001, Neuroscience letters.

Differentiation of species and strains among filamentous fungi by DNA fingerprinting

B. Beyermann, J. Epplen, W. Meyer, 1991, Current Genetics.

SCA2 alleles are not general predisposition factors for multiple sclerosis

J. Epplen, D. Poehlau, B. Miterski, 2000, Neurogenetics.

Is the retina affected in Huntington disease?

R. Dermietzel, J. Epplen, J. Andrich, 2005, Acta Neuropathologica.

In the European population HLA-class II genes are not associated with Helicobacter pylori infection

W. Schmiegel, G. Faller, J. Epplen, 2002, European journal of gastroenterology & hepatology.

Cyclic AMP phosphodiesterase in Leydig cell preparations of the rat testis.

J. Schmidtke, W. Engel, J. Epplen, 1981, Differentiation; research in biological diversity.

Congenic AB mice: A novel means for studying the (molecular) genetics of aggression

R. Schneider-Stock, J. Epplen, 1995, Behavior genetics.

Location of the genes controlling H-Y antigen expression and testis determination on the mouse Y chromosome.

E. Simpson, P. Koopman, J. Epplen, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Haemoglobin freiburg: direct detection by synthetic oligonucleotide probes

J. Epplen, E. Kohne, J. Horst, 1988, Human Genetics.

No association between polymorphisms in the BDNF gene and age at onset in Huntington disease

J. Epplen, J. Andrich, Amer-Denis Akkad, 2006, BMC Medical Genetics.

A human Y-chromosomal DNA sequence expressed in testicular tissue.

J. Schmidtke, W. Engel, J. Epplen, 1987, Nucleic acids research.

Sarcoglycanopathies: Can muscle immunoanalysis predict the genotype?

K. Bushby, J. Epplen, G. Dekomien, 2008, Neuromuscular Disorders.

Smaller caliber renal arteries are a novel feature of uromodulin-associated kidney disease.

D. Blondin, M. Litwin, A. Więcek, 2015, Kidney international.

Glutathione S-Transferase Ω 1 variation does not influence age at onset of Huntington's disease

J. Epplen, J. Andrich, C. Saft, 2004, BMC Medical Genetics.

Characterization of hypervariable locus-specific probes derived from a (CAC)5/(GTG)5 multilocus fingerprint in various Eurasian populations

A. Czeizel, P. Nürnberg, J. Epplen, 1992, Human Genetics.

A newborn with Pierre Robin sequence after preconceptional mitoxantrone exposure of a female with multiple sclerosis

R. Gold, A. Chan, J. Epplen, 2011, Journal of the Neurological Sciences.

Genetic paternity analyses in Little Owls (Athene noctua): does the high rate of paternal care select against extra-pair young?

J. Epplen, T. Lubjuhn, W. Müller, 2001, Journal für Ornithologie.

Genetic paternity analyses in Little Owls (Athene noctua): does the high rate of paternal care select against extra‐pair young?

J. Epplen, T. Lubjuhn, W. Müller, 2001 .

Are there specific genetic risk factors for the different forms of ANCA-associated vasculitis?

J. Epplen, D. Millar, L. Arning, 2010, Annals of the rheumatic diseases.

Genetic and population study of a Y-linked tetranucleotide repeat DNA polymorphism with a simple non-isotopic technique

J. Epplen, F. R. Santos, S. Pena, 1993, Human Genetics.

Acute demyelination in children: predicting pediatric multiple sclerosis manifestation

J. Epplen, S. Hoffjan, 2011 .

Simple repetitive sequences are associated with differentiation of the sex chromosomes in the guppy fish

M. Schmid, J. Epplen, I. Nanda, 1990, Journal of Molecular Evolution.

Simple GACTA repeats characterize the X chromosomal heterochromatin of Microtus agrestis, European field vole (Rodentia, Cricetidae)

K. Sperling, J. Epplen, I. Nanda, 2004, Chromosoma.

Familial parkinsonism with synuclein pathology: Clinical and PET studies of A30P mutation carriers

R. P. Maguire, R. Krüger, L. Schöls, 2001 .

Isolation and characterization of microsatellite markers in the nuclear genome of the brown alga Laminaria digitata (Phaeophyceae)

A. Estoup, B. Kloareg, S. Rousvoal, 1998, Molecular ecology.

Dispensable and indispensable genes in an ameiotic fish, the Amazon molly Poecilia formosa

M. Schartl, M. Schmid, J. Epplen, 1998, Cytogenetic and Genome Research.

Indirect gene diagnoses for complex (multifactorial) diseases--a review.

J. Epplen, J T Epplen, J. Buitkamp, 1995, Gene.

Interdependent MHC-DRB exon-plus-intron evolution in artiodactyls.

J. Epplen, A. Crawford, J. Buitkamp, 1994, Molecular biology and evolution.

Detection of somatic changes in human renal cell carcinomas with oligonucleotide probes specific for simple repeat motifs

W. Wilmanns, H. Höfler, G. Jakse, 1993, Genes, chromosomes & cancer.

Oligonucleotide fingerprinting as a means to identify and survey long-term cultured B cell hybridomas and T cell lines.

J. Hampe, R. Grunow, P. Nürnberg, 1992, Human antibodies and hybridomas.

Base sequence of a cloned snake W-chromosome DNA fragment and identification of a male-specific putative mRNA in the mouse.

S. Ohno, J. Epplen, J. Epplen, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes

G. Oliveira, J. Epplen, P. Maciel, 2011, Brain and Development.

Isolation of microsatellite loci for paternity testing in Phillyrea angustifolia L. (Oleaceae)

J. Epplen, P. Saumitou-Laprade, C. Hardt, 2000, Molecular ecology.

DNA Profiling and DNA Fingerprinting

J. Epplen, T. Lubjuhn, 1999, Methods and Tools in Biosciences and Medicine.

Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsy

O. Riess, J. Epplen, T. Sander, 1999, Epilepsy Research.

Genetic monogamy in burrowing parrots Cyanoliseus patagonus

J. Epplen, T. Lubjuhn, P. Quillfeldt, 2002 .

Pair identity — An important factor concerning variation in extra-pair paternity in the coal tit (Parus ater)

T. Schmoll, V. Dietrich, W. Winkel, 2004 .

cDNA cloning and expression of rsca1, the rat counterpart of the human spinocerebellar ataxia type 1 gene.

P. Wahle, O. Riess, J. Epplen, 1996, Human molecular genetics.

Patterns of cyclic AMP phosphodiesterases during rat testis development

J. Schmidtke, W. Engel, J. Epplen, 1980, Human Genetics.

Cyclic AMP phosphodiesterases of the rat ovary. Oestrous cycle dependent activity change of high affinity form.

J. Schmidtke, J. Epplen, H. Meyer, 1980, Acta endocrinologica.

DNA Fingerprinting: Approaches and Applications

Ranajit Chakraborty, R. Chakraborty, J. Epplen, 1991, Experientia Supplementum.

Tracing the origin of 'blue Weimaraner' dogs by molecular genetics.

J. Epplen, G. Dekomien, W. M. Gerding, 2011, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

DNA fingerprinting in cattle using oligonucleotide probes.

J. Epplen, H. Geldermann, H. Zischler, 2009, Animal genetics.

Generalized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B gene

J. Epplen, G. Dekomien, R. Goedde, 2000, Cytogenetic and Genome Research.

Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

L. Schöls, H. Przuntek, O. Riess, 1997, Annals of neurology.

Bibliography of Ulrich Wolf

C. Tyler-Smith, P. Yen, K. Hirschhorn, 2001, Cytogenetic and Genome Research.

Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington’s disease-like phenotype

P. Bauer, O. Riess, A. Rolfs, 2004, Journal of Medical Genetics.

Species-level differentiation of two cryptic species pairs of wild cavies, genera Cavia and Galea, with a discussion of the relationship between social systems and phylogeny in the Caviinae

F. Trillmich, J. Epplen, G. Dekomien, 2004 .

Monogamy in a new species of wild guinea pigs (Galea sp.)

J. Epplen, C. Hohoff, N. Sachser, 2002, Naturwissenschaften.

BEHAVIOURAL STRATEGIES, TESTIS SIZE, AND REPRODUCTIVE SUCCESS IN TWO CAVIOMORPH RODENTS WITH DIFFERENT MATING SYSTEMS

J. Epplen, N. Sachser, Anja Keil, 1999 .

Oligonucleotide fingerprinting reveals various probe-dependent levels of informativeness in chickpea (Cicer arietinum)

G. Kahl, J. Epplen, K. Weising, 1992 .

Mammalian T-lymphocyte antigen receptor genes: genetic and nongenetic potential to generate variability

J. Chluba, J. Epplen, A. Hinkkanen, 1987, Human Genetics.

On simple repeated GATCA sequences in animal genomes: a critical reappraisal.

J. Epplen, 1988, The Journal of heredity.

The ATG16L1 Gene Variants rs2241879 and rs2241880 (T300A) Are Strongly Associated With Susceptibility to Crohn's Disease in the German Population

B. Müller-Myhsok, T. Mussack, S. Brand, 2008, The American Journal of Gastroenterology.

DNA diagnosis of human genetic individuality

J. Epplen, S. Pena, V. Prado, 1995, Journal of Molecular Medicine.

Indirect DNA/gene diagnoses via electrophoresis – an obsolete principle?

O. Riess, J. Epplen, J. Buitkamp, 1995, Electrophoresis.

Immunoprinting reveals different genetic bases for (auto)immune diseases

J. Epplen, J. Buitkamp, C. Epplen, 1995, Electrophoresis.

Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families.

J. Epplen, G. Dekomien, E. Petrasch‐Parwez, 2015, Investigative ophthalmology & visual science.

Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs

R. Gasser, J. Epplen, W. M. Gerding, 2015, Canine Genetics and Epidemiology.

Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans.

J. Ilonen, M. Ban, A. Goris, 2006 .

Contrasting DNA sequence organisation patterns in sauropsidian genomes

J. Schmidtke, W. Engel, J. Epplen, 1979, Chromosoma.

Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening.

J. Epplen, G. Dekomien, S. Hoffjan, 2014, Molecular and Cellular Probes.

Genetic predisposition to multiple sclerosis as revealed by immunoprinting

H. Przuntek, J. Malin, F. Weber, 1997, Annals of neurology.

Association between shorter leukocyte telomeres and multiple sclerosis

S. Ocklenburg, J. Epplen, A. Haghikia, 2020, Journal of Neuroimmunology.

Analysis of an IFN-gamma gene (IFNG) polymorphism in multiple sclerosis in Europe: effect of population structure on association with disease.

A. Goris, T. Olsson, G. Opdenakker, 1999, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

Unusual Charcot–Marie–Tooth phenotype due to a mutation within the intracellular domain of myelin protein zero

R. Gold, J. Epplen, W. M. Gerding, 2010, Muscle & nerve.

Inhibitors in the NFκB cascade comprise prime candidate genes predisposing to multiple sclerosis, especially in selected combinations

S. Böhringer, J. Epplen, W. Klein, 2002, Genes and Immunity.

Inheritance and mutation of hypervariable (GATA)n microsatellite loci in a moth, Ephestia kuehniella

J. Epplen, D. Weichenhan, J. Rohwedel, 1992 .

Elevated telomerase activity, c‐MYC‐, and hTERT mRNA expression: association with tumour progression in malignant lipomatous tumours

R. Schneider-Stock, A. Roessner, B. Peters, 2003, The Journal of pathology.

Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

Melvin G McInnis, Olaf Riess, Christopher A Ross, 1999, Nature Genetics.

A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity

J. Epplen, L. Arning, M. Genčík, 2003, Human mutation.

DNA sequence organisation in avian genomes

J. Schmidtke, W. Engel, J. Epplen, 1978, Chromosoma.

PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease

A. Chan, J. Epplen, A. Haghikia, 2011, Molecular Neurodegeneration.

The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases

A. Ludolph, J. Epplen, A. Sperfeld, 2013, neurogenetics.

Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.

A. Ziegler, O. Riess, J. Epplen, 1999, American journal of medical genetics.

Mapping, genomic structure, and polymorphisms of the human GABABR1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsy

O. Riess, J. Epplen, B. Bettler, 1998, Neurogenetics.

Genetically distinct clinical subsets, and associations with asthma and eosinophil abundance, within Eosinophilic Granulomatosis with Polyangiitis

William J. Astle, Kenneth G. C. Smith, C. Wallace, 2018, bioRxiv.

Paternity analysis of alternative male reproductive routes among the langurs (Semnopithecus entellus) of Ramnagar

J. Epplen, P. Winkler, C. Hardt, 2001, Animal Behaviour.

Alternative Reproductive Tactics and Reproductive Success in Male Rhesus Macaques

P. Nürnberg, J. Schmidtke, J. Epplen, 1994 .

Changes of telomere lengths in human intracranial tumours

F. Weber, P. Nürnberg, J. Epplen, 1993, Human Genetics.

On the stability of dispensable constituents of the eukaryotic genome: stability of coding sequences versus truly hypervariable sequences in a clonal vertebrate, the amazon molly, Poecilia formosa.

M. Schartl, M. Schmid, J. Epplen, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Genomic stability in malignant melanoma of Xiphophorus

M. Schartl, J. Epplen, Katrin Zunker, 2006, Melanoma research.

Prokaryotic Genomics

Gonzalo Giribet, Rob DeSalle, R. DeSalle, 2003, Methods and Tools in Biosciences and Medicine.

SOX9 Duplication Linked to Intersex in Deer

P. Nürnberg, N. Young, R. Gasser, 2013, PloS one.

Human DNA sequences isolated with an immunoglobulin switch region probe: sequence, chromosomal localization, and restriction fragment length polymorphisms

J. Schmidtke, J. Epplen, C. Bostock, 1986, Human Genetics.

Testis-organizing H-Y antigen as a discrete protein; Its MHC restricted immune recognition and the genomic environment in which H-Y gene operates

S. Ohno, J. Epplen, S. Sutou, 2004, Human Genetics.

Heterogeneity in the Sxr (sex-reversal) locus of the mouse as revealed by synthetic probes

J. Epplen, A. Mclaren, R. Studer, 1988 .

Heterogeneity in the Sxr (sex-reversal) locus of the mouse as revealed by synthetic GATA-GACA probes.

J. Epplen, A. Mclaren, R. Studer, 1988, Genetical research.

Cloning and sequencing of expressed DRB genes of the red deer (Cervus elaphus) Mhc

J. Epplen, G. Buchan, J. Griffin, 2004, Immunogenetics.

Modern genome research and DNA diagnostics in domestic animals in the light of classical breeding techniques

J. Epplen, J. Buitkamp, 1996, Electrophoresis.

Analytical biotechnology

J. Epplen, 2002, Methods and Tools in Biosciences and Medicine.

An Isoform of Ataxin‐3 Accumulates in the Nucleus of Neuronal Cells in Affected Brain Regions of SCA3 Patients

T. Klockgether, O. Riess, J. Epplen, 1998, Brain pathology.

Pseudomale behaviour and spontaneous masculinization in the all-female teleost Poecilia formosa (Teleostei: Poeciliidae)

M. Schartl, M. Schmid, J. Epplen, 1992 .

Heterogeneities in the distribution of (GACA)n simple repeats in the karyotypes of primates and mouse

M. Schmid, J. Epplen, I. Nanda, 1990, Human Genetics.

Male polymorphism inLimia perugiae (Pisces: Poeciliidae)

M. Schartl, M. Schmid, J. Epplen, 1994, Behavior genetics.

DNA Fingerprints in Plants Using Simple-sequence Repeat and Minisatellite Probes

A. Adato, J. Epplen, M. Gomolka, 1995 .

Reproductive failure of dominant males in the poeciliid fish Limia perugiae determined by DNA fingerprinting.

M. Schartl, M. Schmid, J. Epplen, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Which home for coelacanth?

S. Pääbo, M. Schartl, H. Fricke, 1993, Nature.

High mating success of low rank males in Limia perugiae (Pisces: Poeciliidae) as determined by DNA fingerprinting

M. Schartl, M. Schmid, J. Epplen, 1993 .

The gynogenetic reproduction of diploid and triploid hybrid spined loaches (Cobitis: Teleostei), and their ability to establish successful clonal lineages—on the evolution of polyploidy in asexual vertebrates

J. Epplen, K. Janko, P. Kotlík, 2007, Genetica.

EVIDENCE FOR A MONOPHYLETIC ORIGIN OF TRIPLOID CLONES OF THE AMAZON MOLLY, POECILIA FORMOSA

M. Schartl, J. Epplen, K. P. Lampert, 2005, Evolution; international journal of organic evolution.

Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs

R. Gasser, J. Epplen, W. M. Gerding, 2015, Canine Genetics and Epidemiology.

Selected bibliography of Susumu Ohno

C. Disteche, B. Migeon, B. Kerem, 1998, Cytogenetic and Genome Research.

Mating System and Sexual Selection in the Scorpionfly Panorpa vulgaris (Mecoptera: Panorpidae)

J. Epplen, T. Lubjuhn, K. P. Sauer, 1998, Naturwissenschaften.

Genome-wide profiling of S/MAR-based replicon contact sites

H. Lipps, J. Epplen, A. Gogol-Döring, 2017, Nucleic acids research.

Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

K. Hameister, J. Epplen, M. Meins, 2005, Journal of Medical Genetics.

Increased detectability of somatic changes in the DNA from human tumours after probing with “synthetic” and “genome-derived” hypervariable multilocus probes

O. Issinger, J. Epplen, P. Lagoda, 1989, Human Genetics.

On the potential of simple repetitive DNA for fingerprinting in clinical, forensic, and evolutionary dynamic studies

L. Roewer, J. Epplen, G. Melmer, 1992, The clinical investigator.

DNA fingerprinting. Simple repeat loci as tools for genetic identification.

S. Hummel, B. Herrmann, J. Epplen, 1994 .

NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner

J. Epplen, J. Andrich, C. Saft, 2007, Human Genetics.

Avoiding errors in the diagnosis of (CAG)n expansion in the huntingtin gene.

O. Riess, J. Epplen, C. Holzmann, 1997, Journal of medical genetics.

Sequence organization of animal nuclear DNA

J. Schmidtke, J. Epplen, 2004, Human Genetics.

On Interspersed Repetitive DNA Sequences in Animals

J. Epplen, R. Studer, 1990 .

Myelin Water Fraction Imaging Reveals Hemispheric Asymmetries in Human White Matter That Are Associated with Genetic Variation in PLP1

O. Güntürkün, S. Ocklenburg, B. Mädler, 2018, Molecular Neurobiology.

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds

R. Krüger, H. Przuntek, O. Riess, 1998, Journal of neurology, neurosurgery, and psychiatry.

Spinocerebellar Ataxia Type 2: Genotype and Phenotype in German Kindreds

S. Pulst, L. Schöls, H. Przuntek, 1997 .

Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14.

T. Wienker, O. Riess, A. Reis, 1999, American journal of medical genetics.

Primitive sex chromosomes in poeciliid fishes harbor simple repetitive DNA sequences.

M. Schartl, M. Schmid, J. Epplen, 1993, The Journal of experimental zoology.

The genetics of atopic dermatitis: recent findings and future options

J. Epplen, S. Hoffjan, 2005, Journal of Molecular Medicine.

Combinations of Susceptibility Genes Are Associated with Higher Risk for Multiple Sclerosis and Imply Disease Course Specificity

R. Gold, J. Epplen, A. Haghikia, 2015, PloS one.

Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability

R. Gold, J. Epplen, F. Weiler, 2015, neurogenetics.

Genetic modifiers of Huntington’s disease: beyond CAG

J. Epplen, L. Arning, Jörg T. Epplen, 2012 .

Long-term fitness consequences of female extra-pair matings in a socially monogamous passerine

T. Schmoll, V. Dietrich, W. Winkel, 2003, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Complex genetic predisposition in adult and juvenile rheumatoid arthritis

J. Epplen, W. Klein, B. Miterski, 2004, BMC Genetics.

Multiple Sclerosis Severity Score: Using disability and disease duration to rate disease severity

G. Salemi, M. Trojano, G. Edan, 2005, Neurology.

Oligonucleotide fingerprinting of tomato DNA

B. Beyermann, J. Epplen, T. Börner, 1995 .

On genetic components in autoimmunity: a critical review based on evolutionarily oriented rationality

J. Epplen, 1992, Human Genetics.

Alec J. Jeffreys – Born a scientist

J. Epplen, 2013 .

DNA Fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations

L. Roewer, K. Sperling, P. Nürnberg, 1989, Human Genetics.

DNA finger printing by oligonucleotide probes specific for simple repeats

J. Epplen, C. Müller, S. Ali, 1986, Human Genetics.

Aspects of Tandemly Organized, Repetitive Sequences in Chromosomal DNA

J. Epplen, A. Epplen-Haupt, 2002 .

Multilocus DNA Fingerprinting Using Oligonucleotide Probes in 5 Macaque Species

R. Martin, J. Pastorini, J. Epplen, 2000, Folia Primatologica.

Simple Repetitive Sequences in DNA Databanks

J. Epplen, E. Santos, 1997 .

(GTG)5 allows the distinction between different isolates of the nematode Caenorhabditis elegans

E. Schierenberg, J. Epplen, M. Benecke, 1996, Electrophoresis.

Exploiting the informativity of 'meaningless' simple repetitive DNA from indirect gene diagnosis to multilocus genome scanning.

J. Epplen, C. Epplen, W. Mäueler, 1994, Biological chemistry Hoppe-Seyler.

Simple repetitive (GAA)n loci in the human genome

O. Riess, J. Epplen, C. Epplen, 1993, Electrophoresis.

Oligonucleotide Fingerprinting in Plants and Fungi

J. Ramser, G. Kahl, J. Epplen, 1991 .

Oligonucleotide fingerprinting using simple repeat motifs: a convenient, ubiquitously applicable method to detect hypervariability for multiple purposes.

L. Roewer, J. Epplen, H. Zischler, 1991, EXS.

Individual-Specific DNA Fingerprinting in Man Using the Oligonucleotide Probe (GTG)5/(CAC)5

J. Epplen, H. Pöche, V. Schneider, 1991, European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies.

Patterns of sperm use in the scorpionfly Panorpa germanica L. (Mecoptera: Panorpidae)

J. Epplen, K. P. Sauer, C. Hardt, 2006, Behavioral Ecology and Sociobiology.

Distribution and stability of supernumerary microchromosomes in natural populations of the Amazon molly, Poecilia formosa

M. Schartl, M. Schmid, J. Epplen, 2004, Cytogenetic and Genome Research.

Various Levels of (Epi)Genetic Diversities as Demonstrable via Simple Repeated Sequences

J. Epplen, W. Mäueler, C. Epplen, 1999 .

DNA fingerprinting for paternity and maternity in group O Cayo Santiago-derived rhesus monkeys at the German Primate Center: results of a pilot study.

W. Kaumanns, J. Schmidtke, J. Epplen, 1989, Puerto Rico health sciences journal.

Digoxigenated oligonucleotide probes specific for simple repeats in DNA fingerprinting and hybridization in situ

M. Schmid, J. Epplen, I. Nanda, 1989, Human Genetics.

Parentage analyses in the Pied FlycatcherFicedula hypoleuca at the western boundary of its Central European range

W. Winkel, J. Epplen, T. Lubjuhn, 1996 .

Paternity Testing by Oligonucleotide DNA Fingerprinting: A Multi-Center Study Proving Reliability and Validity

J. Hampe, M. Krawczak, P. Nürnberg, 1994 .

Functional characterization of the human Huntington's disease gene promoter.

O. Riess, J. Epplen, C. Holzmann, 2001, Brain research. Molecular brain research.

The paradox of MHC-DRB exon/intron evolution: α-helix and β-sheet encoding regions diverge while hypervariable intronic simple repeats coevolve with β-sheet codons

J. Epplen, A. Crawford, F. Schwaiger, 1993, Journal of Molecular Evolution.

Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24‐q26.31 with minimal overlap to the dup(3q) critical region

J. Epplen, M. Meins, F. Gerresheim, 2005, American journal of medical genetics. Part A.

(CAC)5, a very informative oligonucleotide probe for DNA fingerprinting.

J. Epplen, H. Zischler, J. Epplen, 1988, Nucleic acids research.

Spotted Weimaraner dog due to de novo KIT mutation.

J. Epplen, W. M. Gerding, D. Akkad, 2013, Animal genetics.

Amplification of (GACA)n simple repeats in an exceptional 14p+ marker chromosome

C. Steinlein, M. Schmid, J. Epplen, 1994, Human Genetics.

TPP2 mutation associated with sterile brain inflammation mimicking MS

T. Wieland, A. Deutschländer, T. Strom, 2018, Neurology: Genetics.

TPP 2 mutation associated with sterile brain in fl ammation mimicking MS

T. Wieland, A. Deutschländer, T. Strom, 2022 .

Activation of NPY-Y2 receptors ameliorates disease pathology in the R6/2 mouse and PC12 cell models of Huntington's disease

R. Gold, J. Epplen, C. Saft, 2018, Experimental Neurology.

Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome.

B. Bohnhorst, J. Schmidtke, J. Epplen, 2010, European journal of medical genetics.

rs1004819 Is the Main Disease-Associated IL23R Variant in German Crohn's Disease Patients: Combined Analysis of IL23R, CARD15, and OCTN1/2 Variants

Wolfram Klein, Bertram Müller-Myhsok, Thomas Mussack, 2007, PloS one.

DNA fingerprinting of trait-selected mouse lines and linkage analysis in reference families.

G. Brockmann, L. Bünger, J. Epplen, 1993, EXS.

Gene symbol: RYR1. Disease: malignant hyperthermia.

J. Epplen, G. Dekomien, M. Genčík, 2005, Human genetics.

Novel mutation in the RYR1 gene (R2454C) in a patient with malignant hyperthermia

J. Epplen, M. Genčík, W. Mortier, 2000, Human mutation.

Vb6 T-cell receptor elements in artiodactyls: conservation and germline polymorphisms

J. Epplen, J. Buitkamp, F. Schwaiger, 1993, Mammalian Genome.

Novel members and germline polymorphisms in the human T-cell receptor Vb6 family

J. Epplen, J. Buitkamp, M. Gomolka, 2004, Immunogenetics.

Respiratory insufficiency as a presenting symptom of LGMD2D in adulthood.

B. Schlotter-Weigel, Hanns Lochmüller, D. Pongratz, 2004, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

The Wegener’s granulomatosis quantitative trait locus on chromosome 6p21.3 as characterised by tagSNP genotyping

M. Nothnagel, J. Epplen, L. Arning, 2007, Annals of the rheumatic diseases.

Oligonucleotide fingerprinting of free-ranging and captive rhesus macaques from Cayo Santiago: paternity assignment and comparison of heterozygosity.

M. Krawczak, P. Nürnberg, J. Schmidtke, 1993, EXS.

DNA fingerprinting with simple repetitive oligonucleotide probes in forensic medicine

J. Epplen, G. Wrobel, H. Pöche, 1990 .

Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease

R. Krüger, L. Schöls, H. Przuntek, 2003, Journal of Neural Transmission.

Association of serotonin-1A and -2A receptor promoter polymorphisms with depressive symptoms, functional recovery, and pain in patients 6months after lumbar disc surgery

Kirsten Schmieder, Albrecht Harders, Jörg T. Epplen, 2013, PAIN®.

Association of serotonin-1 A and-2 A receptor promoter polymorphisms with depressive symptoms , functional recovery , and pain in patients 6 months after lumbar disc surgery

Kirsten Schmieder, Albrecht Harders, Jörg T. Epplen, 2013 .

Trinucleotide Repeat Expansions: Mechanisms and Disease Associations

J. Epplen, S. Wieczorek, 2007 .

Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene

J. Epplen, G. Dekomien, E. Petrasch‐Parwez, 2010, neurogenetics.

Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR

N. Dahmen, M. Vorgerd, J. Epplen, 2004, Journal of Neurology.

Novel γ‐sarcoglycan‐mutation affects cardiac function and N‐terminal dystrophin expression

F. Heppner, H. Goebel, W. Stenzel, 2014, Muscle & nerve.

Cross-hybridizing snake satellite, Drosophila, and mouse DNA sequences may have arisen independently.

J. Marsh, G. Gutman, G. Levinson, 1985, Molecular biology and evolution.

ASK1 and MAP2K6 as modifiers of age at onset in Huntington’s disease

D. Monté, J. Epplen, J. Andrich, 2008, Journal of Molecular Medicine.

Increased susceptibility to sporadic Parkinson's disease by a certain combined α‐synuclein/apolipoprotein E genotype

R. Krüger, L. Schöls, D. Berg, 1999, Annals of neurology.

Isolated loss of γ‐sarcoglycan: Diagnostic implications in autosomal recessive limb‐girdle muscular dystrophies

J. Malin, M. Vorgerd, J. Epplen, 2001, Muscle & nerve.

On simple repetitive DNA sequences and complex diseases

P. V. van Helden, J. Epplen, J. Epplen, 1997, Electrophoresis.

Failure to confirm influence of Methyltetrahydrofolate reductase (MTHFR) polymorphisms on age at onset of Huntington disease

J. Epplen, J. Andrich, C. Saft, 2005, Journal of Negative Results in BioMedicine.

Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization

Christian Beste, Sebastian Ocklenburg, Larissa Arning, 2011, Behavioural Brain Research.

The primitive code and repeats of base oligomers as the primordial protein-encoding sequence.

S. Ohno, J. Epplen, 1983, Proceedings of the National Academy of Sciences of the United States of America.

An attempt to approach the molecular mechanisms of primary sex determination: W‐ and Y‐chromosomal conserved simple repetitive DNA sequences and their differential expression in mRNA

S. Ohno, J. Epplen, S. Romero, 1983 .

Variation between and within colonies in the termite: morphology, genomic DNA, and behaviour

R. Brandl, J. Epplen, C. Husseneder, 1998 .

NPY2-receptor variation modulates iconic memory processes

C. Beste, A. Stock, J. Epplen, 2014, European Neuropsychopharmacology.

Electrophoresis of DNA in human genetic diagnostics – state‐of‐the‐art, alternatives and future prospects

J. Epplen, G. Dekomien, L. Arning, 2006, Electrophoresis.

Toward the complete genomic map and molecular pathology of human chromosome 4

O. Riess, J. Epplen, Birgit Winkelmann, 1994, Human Genetics.

Genome analysis of Amphioxus and speculation as to the origin of contrasting vertebrate genome organization patterns.

J. Schmidtke, W. Engel, J. Epplen, 1979, Comparative biochemistry and physiology. B, Comparative biochemistry.

Association between a cannabinoid receptor gene (CNR1) polymorphism and cannabinoid-induced alterations of the auditory event-related P300 potential

G. Juckel, J. Gallinat, J. Epplen, 2011, Neuroscience Letters.

CNR1 variation is associated with the age at onset in Huntington disease.

J. Epplen, C. Saft, L. Arning, 2013, European journal of medical genetics.

Endocannabinergic modulation of central serotonergic activity in healthy human volunteers

G. Juckel, D. Tsikas, J. Epplen, 2023, Annals of General Psychiatry.

rs224136 on Chromosome 10q21.1 and Variants in PHOX2B, NCF4, and FAM92B Are Not Major Genetic Risk Factors for Susceptibility to Crohn's Disease in the German Population

B. Müller-Myhsok, T. Mussack, S. Brand, 2009, The American Journal of Gastroenterology.

Genomic simple repetitive DNAs are targets for differential binding of nuclear proteins

J. Epplen, J. Epplen, A. Kyas, 1996, FEBS letters.

A functionally relevant IRF5 haplotype is associated with reduced risk to Wegener’s granulomatosis

J. Epplen, S. Müller, S. Wieczorek, 2010, Journal of Molecular Medicine.

Evidence for STAT4 as a Common Autoimmune Gene: rs7574865 Is Associated with Colonic Crohn's Disease and Early Disease Onset

B. Müller-Myhsok, S. Brand, J. Glas, 2010, PloS one.

Altered electrophoretic behavior of DNA due to short‐time UV‐B irradiation

J. Epplen, A. Kyas, W. Mäueler, 1994, Electrophoresis.

Differential stability of the (GAA)n tract in the Friedreich ataxia (STM7) gene

L. Schöls, J. Epplen, B. Miterski, 1997, Human Genetics.

High telomerase activity and high HTRT mRNA expression differentiate pure myxoid and myxoid/round‐cell liposarcomas

R. Schneider-Stock, A. Roessner, J. Epplen, 2000, International journal of cancer.

Isolation and characterization of the rat huntingtin promoter.

O. Riess, J. Epplen, D. Petersohn, 1998, The Biochemical journal.

Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during development.

O. Riess, H. Hameister, J. Epplen, 1995, Human molecular genetics.

Predominant neuronal expression of the gene responsible for dentatorubral-pallidoluysian atrophy (DRPLA) in rat.

O. Riess, J. Epplen, I. Schmitt, 1995, Human molecular genetics.

Modifying effects of the R389G beta1-adrenoceptor polymorphism on resting heart rate and blood pressure in patients with obstructive sleep apnoea.

J. Epplen, B. Sanner, A. Mügge, 2006, Clinical science.

Modifying effects of the R 389 G β 1-adrenoceptor polymorphism on resting heart rate and blood pressure in patients with obstructive sleep apnoea

J. Epplen, A. Mügge, L. Rump, 2005 .

SEX-DETERMINING GENES AND GENE REGULATION

S. Ohno, J. Epplen, J. McCarrey, 1981 .

Genetic background of apparently idiopathic sporadic cerebellar ataxia

L. Schöls, H. Przuntek, O. Riess, 2000, Human Genetics.

GENOMIC INSTABILITY IN COLORECTAL CARCINOMAS: COMPARISON OF DIFFERENT EVALUATION METHODS AND THEIR BIOLOGICAL SIGNIFICANCE

J. Rüschoff, J. Schlegel, J. Epplen, 1996, The Journal of pathology.

Handedness and the X chromosome: The role of androgen receptor CAG-repeat length

M. Falkenstein, O. Güntürkün, S. Ocklenburg, 2015, Scientific Reports.

Morbus Huntington – a human genetic model disease

H. Przuntek, J. Epplen, C. Saft, 2001, Cytogenetic and Genome Research.

Does the tuberous sclerosis complex include clivus chordoma? A case report

J. Epplen, J. Börgel, B. Miterski, 2001, European Journal of Pediatrics.

Disgust in pre-clinical Huntington's disease: A longitudinal study

A. W. Young, A. Young, R. Sprengelmeyer, 2006, Neuropsychologia.

WITHIN-COLONY RELATEDNESS IN A TERMITE SPECIES: GENETIC ROADS TO EUSOCIALITY?

R. Brandl, J. Epplen, M. Kaib, 1999 .

Kin-biased foraging in a termite

R. Brandl, J. Epplen, M. Kaib, 1996, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Ccdc66 null mutation causes retinal degeneration and dysfunction.

J. Kremers, T. Rülicke, R. Dermietzel, 2011, Human molecular genetics.

High gene flow between populations of Macrotermes michaelseni (Isoptera, Termitidae)

R. Brandl, J. Epplen, M. Kaib, 2005, Insectes Sociaux.

R. Brandl, J. Epplen, M. Kaib, 2005, Molecular ecology.

PATERNAL GENETIC EFFECTS ON OFFSPRING FITNESS ARE CONTEXT DEPENDENT: WITHIN THE EXTRAPAIR MATING SYSTEM OF A SOCIALLY: MONOGAMOUS PASSERINE

F. Schurr, T. Schmoll, V. Dietrich, 2005, Evolution; international journal of organic evolution.

Patterns of cyclic AMP phosphodiesterases in the rat pineal gland: sex differences in diurnal rhythmicity.

J. Schmidtke, W. Engel, J. Epplen, 1982, Neuroendocrinology.

Genetic Counselling for Predictive Testing in Huntington's Disease in One Centre since 1993. Gender-Specific Aspects of Decision-Making.

J. Epplen, L. Arning, S. Stemmler, 2015, Journal of Huntington's disease.

Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German origin.

O. Riess, W. Engel, J. Epplen, 1993, Human molecular genetics.

Immunoprinting: various genes are associated with increased risk to develop rheumatoid arthritis in different groups of adult patients

O. Niwa, J. Epplen, E. Albert, 2004, Journal of Molecular Medicine.

Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.

L. Schöls, H. Przuntek, O. Riess, 1996, Journal of neurology, neurosurgery, and psychiatry.

Molecular biology techniques in the diagnosis of monogenic diseases.

J. Epplen, C. Wagener, P. Vihko, 1994, Journal of the International Federation of Clinical Chemistry.

Autonomic nervous system function in Huntington's disease

H. Przuntek, J. Epplen, C. Saft, 2002, Journal of neurology, neurosurgery, and psychiatry.

Friedreich's ataxia. Revision of the phenotype according to molecular genetics.

L. Schöls, H. Przuntek, J. Epplen, 1997, Brain : a journal of neurology.

Evaluation of the γ-synuclein gene in German Parkinson's disease patients

R. Krüger, L. Schöls, H. Przuntek, 2001, Neuroscience Letters.

Mutation analysis and association studies of nuclear factor-κB1 in sporadic Parkinson's disease patients

H. Przuntek, R. Krüger, L. Schöls, 2002, Journal of Neural Transmission.

Refining the results of a whole‐genome screen based on 4666 microsatellite markers for defining predisposition factors for multiple sclerosis

J. Epplen, S. Schimrigk, M. Haupts, 2004, Electrophoresis.

Amplification of microsatellites adapted from human systems in faecal DNA of wild Hanuman langurs (Presbytis entellus)

J. Epplen, P. Winkler, C. Epplen, 1998, Electrophoresis.

Correcting for multiple testing in genetic association studies: the legend lives on

Stefan Boehringer, M. Krawczak, J. Epplen, 2001, Human Genetics.

Genetic association studies of bronchial asthma – a need for Bonferroni correction?

Michael Krawczak, Stefan Boehringer, Stefan Boehringer, 2000, Human Genetics.

Genetic Variability of RXRB, PPARA, and PPARG in Wegener's Granulomatosis

J. Epplen, S. Wieczorek, W. Gross, 2009, PPAR research.

Geographic differences in the allele frequencies of the human Y-linked tetranucleotide polymorphism DYS19

J. Epplen, F. R. Santos, S. Pena, 1996, Human Genetics.

Muscle pain in myophosphorylase deficiency (McArdle’s disease): The role of gender, genotype, and pain-related coping

M. Vorgerd, R. Kley, J. Epplen, 2006, Pain.

On the relevance of the NPY2-receptor variation for modes of action cascading processes

Christian Beste, Ann-Kathrin Stock, Jörg T. Epplen, 2014, NeuroImage.

DRD1 and DRD2 Genotypes Modulate Processing Modes of Goal Activation Processes during Action Cascading

Christian Beste, Ann-Kathrin Stock, Larissa Arning, 2014, The Journal of Neuroscience.

FOXP2 variation modulates functional hemispheric asymmetries for speech perception

O. Güntürkün, S. Ocklenburg, C. Beste, 2013, Brain and Language.

Cholecystokinin A Receptor (CCKAR) Gene Variation Is Associated with Language Lateralization

Onur Güntürkün, Christian Beste, Sebastian Ocklenburg, 2013, PloS one.

Variations in the GRIN2B gene are associated with risky decision-making

C. Beste, J. Epplen, M. C. Stüttgen, 2011, Neuropharmacology.

Genetic distinction of scorpionflies (Panorpa vulgaris) by microsatellites.

J. Epplen, T. Lubjuhn, K. P. Sauer, 1998, Molecular Ecology.

Large males dominate: ecology, social organization, and mating system of wild cavies, the ancestors of the guinea pig

F. Trillmich, J. Epplen, N. Sachser, 2008, Behavioral Ecology and Sociobiology.

Sperm transfer and paternity in the scorpionfly Panorpa cognata: large variance in traits favoured by post-copulatory episodes of sexual selection

J. Epplen, G. Dekomien, L. Engqvist, 2007, Evolutionary Ecology.

Molecular genetic analysis of remating frequencies and sperm competition in the scorpionfly Panorpa vulgaris (Imhoff and Labram)

J. Epplen, T. Lubjuhn, T. Gerken, 1999 .

On ancestors of dog breeds with focus on Weimaraner hunting dogs.

J. Epplen, G. Dekomien, R. Kropatsch, 2011, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

A bisexually reproducing all-triploid vertebrate

M. Schartl, C. Steinlein, J. Epplen, 2002, Nature Genetics.

Body Weight and Rearing Conditions of Males, Female Choice and Paternities in a Small Mammal, Cavia aperea

J. Epplen, G. Dekomien, N. Sachser, 2008 .

Male rank, reproductive behavior, and reproductive success in free-ranging rhesus macaques

P. Nürnberg, J. Schmidtke, J. Epplen, 1993, Primates.

Typing of artiodactyl MHC‐DRB genes with the help of intronic simple repeated DNA sequences

J. Epplen, J. Epplen, J. Buitkamp, 1993, Molecular ecology.

The paradox of MHC-DRB exon/intron evolution: alpha-helix and beta-sheet encoding regions diverge while hypervariable intronic simple repeats coevolve with beta-sheet codons.

J. Epplen, A. Crawford, F. Schwaiger, 1993, Journal of Molecular Evolution.

Coding versus intron variability: extremely polymorphic HLA-DRB1 exons are flanked by specific composite microsatellites, even in distant populations

P. V. van Helden, J. Epplen, J. Guerreiro, 1997, Human Genetics.

DNA sequence organisation in relation to genome size in birds

J. Schmidtke, W. Engel, J. Epplen, 1981, Experientia.

When control fails: Influence of the prefrontal but not striatal dopaminergic system on behavioural flexibility in a change detection task

M. Pinnow, E. Wascher, C. Beste, 2012, Neuropharmacology.

Polyandry in coal tits Parus ater: fitness consequences of putting eggs into multiple genetic baskets

F. Schurr, T. Schmoll, W. Winkel, 2007, Journal of evolutionary biology.

Evaluation of variation in genes of the arylhydrocarbon receptor pathway for an association with multiple sclerosis

J. Epplen, A. Haghikia, S. Hoffjan, 2019, Journal of Neuroimmunology.

Alpha-sarcoglycanopathy previously misdiagnosed as Duchenne muscular dystrophy: implications for current diagnostics and patient care

J. Epplen, U. Schara, M. Genčík, 2001, European Journal of Pediatrics.

The IL‐10 gene is not involved in the predisposition to inflammatory bowel disease

J. Epplen, C. Folwaczny, W. Klein, 2000, Electrophoresis.

Exclusion of the PDE6A gene for generalised progressive retinal atrophy in 11 breeds of dog.

J. Epplen, G. Dekomien, 2000, Animal genetics.

NMDA receptor gene variations as modifiers in Huntington disease: a replication study

J. Schiefer, R. Barker, R. Reilmann, 2011, PLoS currents.

Evaluation of the canine RPE65 gene in affected dogs with generalized progressive retinal atrophy.

J. Epplen, G. Dekomien, 2003, Molecular vision.

PLP1 Gene Variation Modulates Leftward and Rightward Functional Hemispheric Asymmetries

O. Güntürkün, S. Ocklenburg, C. Beste, 2018, Molecular Neurobiology.

Machado-Joseph disease mutations as the genetic basis of most spinocerebellar ataxias in Germany.

L. Schöls, H. Przuntek, O. Riess, 1995, Journal of neurology, neurosurgery, and psychiatry.

Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease

R. Gold, A. Chan, J. Epplen, 2010, Journal of Molecular Medicine.

Novel KIF7 Mutation in a Tunisian Boy with Acrocallosal Syndrome: Case Report and Review of the Literature

J. Epplen, S. Hoffjan, U. Hehr, 2015, Molecular Syndromology.

Towards covering immunological genes with highly informative markers: a trans-species approach.

J. Epplen, J. Buitkamp, M. Gomolka, 1993, EXS.

Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25

O. Riess, J. Epplen, I. Siedlaczck, 1993, Human Genetics.

PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness

M. Falkenstein, O. Güntürkün, S. Ocklenburg, 2013, PloS one.

Multiple sclerosis in families: risk factors beyond known genetic polymorphisms

J. Epplen, R. Linker, A. Haghikia, 2016, neurogenetics.

Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability

R. Gold, J. Epplen, F. Weiler, 2015, Neurogenetics.

A large deletion in RPGR causes XLPRA in Weimaraner dogs

P. Nürnberg, J. Altmüller, J. Epplen, 2016, Canine Genetics and Epidemiology.

Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts

K. Grzeschik, L. Roewer, N. Spurr, 1992, Human Genetics.

Rapid genetic diversification within dog breeds as evidenced by a case study on Schnauzers.

O. Distl, J. Epplen, G. Dekomien, 2012, Animal genetics.

On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors

J. Epplen, W. Klein, L. Arning, 2005, Journal of Negative Results in BioMedicine.

Novel association of the CD226 (DNAM-1) Gly307Ser polymorphism in Wegener's granulomatosis and confirmation for multiple sclerosis in German patients

A. Chan, J. Epplen, S. Hoffjan, 2009, Genes and Immunity.

Age at onset in Huntington’s disease: replication study on the associations of ADORA2A, HAP1 and OGG1

J. Epplen, C. Saft, L. Arning, 2010, neurogenetics.

Haplotype-defined linkage region for gPRA in Schapendoes dogs

T. Dobosz, J. Epplen, G. Dekomien, 2007, Molecular vision.

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

T. Wienker, A. Ziegler, O. Riess, 1997, Neurology.

Worldwide ethnic distribution of the G protein beta3 subunit 825T allele and its association with obesity in Caucasian, Chinese, and Black African individuals.

D. Rosskopf, K. Jöckel, P. Forster, 1999, Journal of the American Society of Nephrology : JASN.

The gene encoding the α 1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy

T. Wienker, O. Riess, J. Epplen, 1998, Epilepsy Research.

AZFc region of the Y chromosome shows singular structural organization

J. Epplen, Sher Ali, J. Srivastava, 2010, Chromosome Research.

Age at onset of Huntington disease is not modulated by the R72P variation in TP53 and the R196K variation in the gene coding for the human caspase activated DNase (hCAD)

J. Epplen, J. Andrich, C. Saft, 2005, BMC Medical Genetics.

Multilocus fingerprinting using oligonucleotide probes reveals a highly polymorphic single locus system in great tits Parus major

J. Epplen, T. Lubjuhn, C. Epplen, 1993 .

Influence of extra-pair paternity on parental care in great tits ( Parus major )

J. Epplen, T. Lubjuhn, E. Curio, 1993 .

An extended association screen in multiple sclerosis using 202 microsatellite markers targeting apoptosis-related genes does not reveal new predisposing factors

J. Epplen, S. Schimrigk, M. Haupts, 2005, Journal of negative results in biomedicine.

Association of age at onset in Huntington disease with functional promoter variations in NPY and NPY2R

J. Epplen, C. Saft, L. Arning, 2014, Journal of Molecular Medicine.

Screening of a mouse/human Y‐chromosomal cosmid library for gene candidates and markers by using (short) oligonucleotide probes

J. Epplen, Jörg T. Epplen, T. Träger, 1994, Electrophoresis.

Early stages of sex chromosome differentiation in fish as analysed by simple repetitive DNA sequences

M. Schartl, M. Schmid, J. Epplen, 1992, Chromosoma.

Mutations in the calcium-sensing receptor: A new genetic risk factor for chronic pancreatitis?

F. Schmitz, J. Epplen, P. Felderbauer, 2006, Scandinavian journal of gastroenterology.

„Syndrom“ multiple Sklerose

R. Gold, J. Epplen, D. Akkad, 2007 .

GENOMIC INSTABILITY IN COLORECTAL CARCINOMAS: COMPARISON OF DIFFERENT EVALUATION METHODS AND THEIR BIOLOGICAL SIGNIFICANCE

J. Rüschoff, J. Schlegel, J. Epplen, 1996, The Journal of pathology.

The bovine interleukin-4 gene: genomic organization, localization, and evolution

J. Epplen, R. Fries, J. Epplen, 1995, Mammalian Genome.

Association of interleukin-8 receptor α polymorphisms with chronic obstructive pulmonary disease and asthma

J. Epplen, G. Rohde, G. Schultze-Werninghaus, 2005, Genes and Immunity.

DNA fingerprinting using non-radioactive oligonucleotide probes specific for simple repeats.

J. Epplen, H. Zischler, R. Schäfer, 1988, Nucleic acids research.

“Pseudodominant inheritance” of ataxia with ocular apraxia type 2 (AOA2)

D. Timmann, R. Schüle, L. Schöls, 2008, Journal of Neurology.

Prospective Evaluation of Predictive DNA Testing for Huntington’s Disease in a Large German Center

S. Ocklenburg, J. Epplen, C. Saft, 2017, Journal of Genetic Counseling.

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease

B. Müller-Myhsok, S. Brand, J. Glas, 2005, Gut.

Trinucleotide repeat expansions in the junctophilin‐3 gene are not found in caucasian patients with a huntington's disease‐like phenotype

C. Ross, P. Bauer, R. Margolis, 2002, Annals of neurology.

Novel SNPs in the CD18 gene validate the association with MPO-ANCA+ vasculitis

J. Epplen, S. Meller, M. Genčík, 2001, Genes and Immunity.

The expression of the evolutionarily conserved GATA/GACA repeats in mouse tissues

J. Epplen, A. Becker, R. Schäfer, 2004, Chromosoma.

Microsatellite evolution in the 5′ UTR of theHLA-F gene

J. Epplen, J. Guerreiro, E. Santos, 1998 .

Microsatellite and HLA class II oligonucleotide typing in a population of Yanomami Indians.

L. Roewer, J. Epplen, M. Nagy, 1993, EXS.

Association of UCP2 −866 G/A polymorphism with chronic inflammatory diseases

M. Pierer, T. Karlsen, K. Boberg, 2009, Genes and Immunity.

Multilocus fingerprinting and single locus analyses in the great tit for paternity determination

J. Epplen, T. Lubjuhn, C. Epplen, 1996, Electrophoresis.

False‐negative finding in rapid interphase FISH analysis of uncultured amniotic cells

J. Epplen, B. Eiben, W. Hammans, 1999, Prenatal diagnosis.

On the essence of "meaningless" simple repetitive DNA in eukaryote genomes.

J. Epplen, G. Melmer, J. Epplen, 1993, EXS.

Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease.

R. Krüger, D. Berg, H. Przuntek, 2000, Neuroreport.

A large deletion in RPGR causes XLPRA in Weimaraner dogs

P. Nürnberg, J. Altmüller, J. Epplen, 2016, Canine Genetics and Epidemiology.

Evaluation of RDS/Peripherin and ROM1 as candidate genes in generalised progressive retinal atrophy and exclusion of digenic inheritance.

J. Epplen, G. Dekomien, M. Runte, 2000, Animal genetics.

Selected di- and tetranucleotide microsatellites from chromosomes 7, 12, 14, and Y in various Eurasian populations

L. Roewer, P. Nürnberg, J. Epplen, 1994, Human Genetics.

Incorporation of subgenomic amounts of DNA as compensation for mutational load in a gynogenetic fish

M. Schartl, M. Schmid, J. Epplen, 1995, Nature.

Calculating paternity probabilities from DNA multilocus fingerprints in some cases of deficiency

J. Epplen, J. Epplen, A. Yassouridis, 1993, Electrophoresis.

Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia

L. Schöls, W. Engel, J. Epplen, 2002, Human mutation.

Spinocerebellar ataxia type 1: clinical and neurophysiological characteristics in German kindreds

L. Schöls, H. Przuntek, O. Riess, 1995, Acta neurologica Scandinavica.

The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy.

T. Wienker, O. Riess, J. Epplen, 1998, Epilepsy Research.

HLA class II disease associations in southern Africa.

P. V. van Helden, J. Epplen, Z. Lombard, 2006, Tissue antigens.

Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophy

J. Epplen, G. Dekomien, 2002, BMC Genetics.

Guillain-Barré syndrome associated with chromosome 17p11.2–12 duplication

J. Weber, J. Epplen, R. Meyer, 2007 .

POLYMORPHISMS IN THE CANINE ROD TRANSDUCIN GENE AND EXCLUSION AS CAUSE FORGENERALISED PROGRESSIVE RETINAL ATROPHY (GPRA): SHORT COMMUNICATION

J. Epplen, W. Klein, G. Dekomien, 1998 .

Different mRNA expression profile during tumor progression in a well-differentiated liposarcoma--A microdissection approach.

R. Schneider-Stock, A. Roessner, C. Boltze, 2003, Pathology, research and practice.

The IL‐10 gene is not involved in the predisposition to inflammatory bowel disease

J. Epplen, C. Folwaczny, W. Klein, 2000, Electrophoresis.

Familial parkinsonism with synuclein pathology

R. Krüger, L. Schöls, K. Leenders, 2001, Neurology.

The CYP2J2 G-50T polymorphism and myocardial infarction in patients with cardiovascular risk profile

T. Holland-Letz, J. Epplen, M. Spiecker, 2008, BMC cardiovascular disorders.

Helicobacter pylori infection and polymorphisms in the tumor necrosis factor region

J. Epplen, S. Suerbaum, U. Peitz, 1999, Electrophoresis.

Chorea Huntington: A Rare Case with Childhood Onset

J. Epplen, N. Wagner, H. Strehl, 2002, Neuropediatrics.

Confidence intervals for predicted age of onset, given the size of (CAG)n repeat, in Huntington's disease

S. Hazout, F. Loirat, J. Epplen, 1995, Human Genetics.

On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors

J. Epplen, W. Klein, L. Arning, 2005, Journal of Negative Results in BioMedicine.

Neurodegeneration in the olfactory bulb and olfactory deficits in the Ccdc66 -/- mouse model for retinal degeneration

J. Epplen, E. Förster, E. Petrasch‐Parwez, 2018, IBRO reports.

The multiple sclerosis severity score

S. Sawcer, X. Montalban, E. Celius, 2003 .

The functional BDNF Val66Met polymorphism affects functions of pre-attentive visual sensory memory processes

C. Beste, J. Epplen, L. Arning, 2011, Neuropharmacology.

N-methyl-d-aspartate receptor 2B subunit (GRIN2B) gene variation is associated with alerting, but not with orienting and conflicting in the Attention Network Test

M. Pinnow, C. Beste, J. Epplen, 2012, Neuropharmacology.

Dissociable electrophysiological subprocesses during response inhibition are differentially modulated by dopamine D1 and D2 receptors

C. Beste, A. Stock, J. Epplen, 2016, European Neuropsychopharmacology.

The G2964A polymorphism of the STAT6 gene in inflammatory bowel disease.

W. Schmiegel, J. Epplen, C. Folwaczny, 2005, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Promoter polymorphism rs3087456 in the MHC class II transactivator gene is not associated with susceptibility for selected autoimmune diseases in German patient groups

J. Epplen, S. Wieczorek, D. A. Akkad, 2006, International journal of immunogenetics.

Apolipoprotein E genotypes do not influence the age of onset in Huntington’s disease

H. Przuntek, J. Epplen, J. Andrich, 2004, Journal of Neurology, Neurosurgery & Psychiatry.