W. Berger

W. Berger, A. Medeiros-Domingo, A. Saguner, 2016, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints

D. Weghuis, R. Sinke, W. Berger, 1993, Human Genetics.

Large genomic fibrillin-1 (FBN1) gene deletions provide evidence for true haploinsufficiency in Marfan syndrome

W. Berger, A. Patrignani, I. Magyar, 2007, Human Genetics.

A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO‐1 and UBC9

W. Berger, A. Zankl, D. Betts, 2005 .

Syndromic choroideremia: sublocalization of phenotypes associated with Martin-Probst deafness mental retardation syndrome.

M. Bach, W. Berger, C. Poloschek, 2008, Investigative ophthalmology & visual science.

Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria.

W. Berger, G. Nürnberg, P. Nürnberg, 2008, American journal of human genetics.

Novel mutations in the folliculin gene associated with spontaneous pneumothorax

H. Alkadhi, W. Berger, E. Russi, 2008, European Respiratory Journal.

Vascular changes in the cerebellum of Norrin /Ndph knockout mice correlate with high expression of Norrin and Frizzled‐4

S. Feil, W. Berger, U. Luhmann, 2008, The European journal of neuroscience.

Retinal vasculature changes in Norrie disease mice.

W. Berger, E. Lütjen-Drecoll, C. May, 1998, Investigative ophthalmology & visual science.

NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein.

S. Freier, H. Scherthan, S. Feil, 2003, Investigative ophthalmology & visual science.

A R T Ic L E

H. Ropers, W. Berger, H. Hameister, 2017 .

A Swiss Patient Cohort Reveals Genetic Predisposition Of Known And New Genetic Loci To AMD And To Intravitreal Ranibizumab (lucentis®) Treatment Outcome

W. Berger, S. Michels, M. Menghini, 2011 .

Cloning of the breakpoints of a deletion associated with choroideremia

F. Cremers, H. Ropers, W. Berger, 1990, Human Genetics.

Year : 2009 Genotyping Microarray for CSNB-Associated Genes

J. Sahel, B. Lorenz, E. Zrenner, 2010 .

Genotyping microarray for CSNB-associated genes.

J. Sahel, B. Lorenz, E. Zrenner, 2009, Investigative ophthalmology & visual science.

Mutations in the MEN I gene in sporadic neuroendocrine tumours of gastroenteropancreatic system

H. Ropers, W. Berger, P. Neuhaus, 1997, The Lancet.

Norrin stimulates cell proliferation in the superficial retinal vascular plexus and is pivotal for the recruitment of mural cells.

S. Feil, W. Berger, Jurian Zuercher, 2012, Human molecular genetics.

Identification of the genetic defect in the original Wagner syndrome family.

W. Berger, D. Bartholdi, B. Kloeckener-Gruissem, 2006, Molecular vision.

Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals CYP1B1 and FOXC1 Variants as Most Frequent Causes

S. Feil, W. Berger, C. Gerth-Kahlert, 2020, Translational vision science & technology.

C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations.

James V. M. Hanson, W. Berger, B. Lam, 2017, Investigative ophthalmology & visual science.

Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retina.

W. Berger, C. Pusch, K. Kohler, 2003, Investigative ophthalmology & visual science.

Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans

W. Berger, S. Bhattacharya, A. Moore, 2019, Front. Physiol..

Associated With Cataract in Mouse and Humans.

W. Berger, S. Bhattacharya, A. Moore, 2019 .

Molecular Dissection of Norrie Disease

W. Berger, Wolfgang Berger, 1998, Cells Tissues Organs.

Intrafamilial variability of the ocular phenotype in a Polish family with a missense mutation (A63D) in the Norrie disease gene.

S. Feil, W. Berger, J. Zaremba, 1998, Ophthalmic genetics.

Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment

W. Berger, C. Gerth-Kahlert, A. Hackenberg, 2022, International journal of molecular sciences.

Long-term Studies On The Anti-VEGF Treatment Success In Age-related Macular Degeneration (amd)

W. Berger, M. Menghini, F. Sutter, 2012 .

Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease-associated genes.

L. Vissers, A. Hoischen, I. Fajardy, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

A Novel NYX Mutation Associated with X-Linked Congenital Stationary Night Blindness in a New Zealand Family

W. Berger, A. Vincent, D. Sharp, 2011 .

A common NYX mutation in Flemish patients with X linked CSNB

W. Berger, C. Zeitz, B. Budde, 2008, British Journal of Ophthalmology.

Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome‐related disorders

W. Berger, C. Boileau, G. Mátyás, 2006, Human mutation.

Development of a genotyping microarray for Usher syndrome

C. Cremers, M. Bitner-Glindzicz, E. van Wijk, 2006, Journal of Medical Genetics.

Ectopic Norrin Induces Growth of Ocular Capillaries and Restores Normal Retinal Angiogenesis in Norrie Disease Mutant Mice

M. Seeliger, E. Zrenner, W. Berger, 2005, The Journal of Neuroscience.

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

F. Riemslag, F. Cremers, W. Berger, 2005, Investigative ophthalmology & visual science.

Unusual retinopathy in a child with severe combined immune deficiency

James V. M. Hanson, W. Berger, C. Gerth-Kahlert, 2018, Ophthalmic genetics.

Long-term consequences of developmental vascular defects on retinal vessel homeostasis and function in a mouse model of Norrie disease

N. Tanimoto, S. Beck, Marina Garcia Garrido, 2017, PloS one.

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

C. Scharfe, A. Meindl, S. Feil, 2000, Nature Genetics.

The molecular basis of human retinal and vitreoretinal diseases

W. Berger, J. Neidhardt, B. Kloeckener‐Gruissem, 2010, Progress in Retinal and Eye Research.

Long-Range PCR-Based NGS Applications to Diagnose Mendelian Retinal Diseases

S. Feil, W. Berger, C. Gerth-Kahlert, 2020, medRxiv.

Norrie disease is caused by mutations in an extracellular protein resembling C–terminal globular domain of mucins

M. Haasemann, T. Meitinger, A. Meindl, 1992, Nature Genetics.

Full-length human L1 insertions retain the capacity for high frequency retrotransposition in cultured cells.

W. Berger, H. Kazazian, U. Schwahn, 1999, Human molecular genetics.

Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.

Olivier Poch, Sabine Defoort-Dhellemmes, Xavier Zanlonghi, 2012, American journal of human genetics.

TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.

T. Léveillard, J. Sahel, S. Jacobson, 2009, American journal of human genetics.

CORRIGENDUM: Nyctalopin is essential for synaptic transmission in the cone dominated zebrafish retina

T. Labhart, W. Berger, S. Neuhauss, 2007, The European journal of neuroscience.

Nyctalopin is essential for synaptic transmission in the cone dominated zebrafish retina

T. Labhart, W. Berger, S. Neuhauss, 2006, The European journal of neuroscience.

Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness.

S. Feil, F. Cremers, W. Berger, 2005, Molecular vision.

Positional cloning of the gene for X-linked retinitis pigmentosa 2

Steffen Lenzner, André Rosenthal, A. Rosenthal, 1998, Nature Genetics.

De Novo Assembly-Based Analysis of RPGR Exon ORF15 in an Indigenous African Cohort Overcomes Limitations of a Standard Next-Generation Sequencing (NGS) Data Analysis Pipeline

W. Berger, R. Ramesar, G. Rebello, 2020, Genes.

A gene therapeutic approach to correct splice defects with modified U1 and U6 snRNPs.

W. Berger, E. Glaus, J. Neidhardt, 2013, Human gene therapy.

U1 snRNA‐mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation

H. Omran, W. Berger, G. Nürnberg, 2011, Human mutation.

Gene therapeutic approach using mutation-adapted U1 snRNA to correct a RPGR splice defect in patient-derived cells.

W. Berger, E. Glaus, J. Neidhardt, 2011, Molecular therapy : the journal of the American Society of Gene Therapy.

Identification and functional characterization of a novel rhodopsin mutation associated with autosomal dominant CSNB.

W. Berger, A. K. Gross, J. Lemke, 2008, Investigative ophthalmology & visual science.

Integrin-linked kinase controls retinal angiogenesis and is linked to Wnt signaling and exudative vitreoretinopathy

S. Feil, W. Berger, R. Adams, 2019, Nature Communications.

Genetic Analysis in a Swiss Cohort of Bilateral Congenital Cataract.

S. Feil, W. Berger, C. Gerth-Kahlert, 2021, JAMA ophthalmology.

Genotype-Phenotype Analysis of a Novel Recessive and a Recurrent Dominant SNRNP200 Variant Causing Retinitis Pigmentosa.

F. Kivrak-Pfiffner, W. Berger, C. Gerth-Kahlert, 2019, Investigative ophthalmology & visual science.

Abnormal creatine transport of mutations in monocarboxylate transporter 12 (MCT12) found in patients with age-related cataract can be partially rescued by exogenous chaperone CD147

T. Wong, W. Berger, Ching-Yu Cheng, 2017, Human molecular genetics.

Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations

W. Berger, P. Nürnberg, H. Thiele, 2016, PloS one.

Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies

W. Berger, C. Gerth-Kahlert, L. Berger, 2016, Scientific Reports.

Application of WES towards Molecular Investigation of Congenital Cataracts: Identification of Novel Alleles and Genes in a Hospital-Based Cohort of South India

W. Berger, J. Graw, I. Magyar, 2020, International journal of molecular sciences.

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

George J. Feldman, Andrea Ballabio, Maximilian Muenke, 1997, Nature Genetics.

Isolation of a candidate gene for Norrie disease by positional cloning

A. Monaco, T. Meitinger, B. Lorenz, 1992, Nature Genetics.

Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases

W. Berger, G. Russo, A. Medeiros-Domingo, 2017, European Journal of Human Genetics.

Therapeutic strategy to rescue mutation‐induced exon skipping in rhodopsin by adaptation of U1 snRNA

W. Berger, F. Pagani, E. Glaus, 2009, Human mutation.

X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications.

Carolyn J. Brown, C. Brown, H. Lehrach, 2001, Human molecular genetics.

ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature

Christian Gilissen, Alexander Hoischen, Tomoko Tahira, 2013, Proceedings of the National Academy of Sciences.

Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.

E. Zrenner, S. Feil, W. Berger, 2006, American Journal of Human Genetics.

Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)

P. Sieving, A. Ballabio, T. Rosenberg, 1998 .

Impact of Genetic Variant Reassessment on the Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy Based on the 2010 Task Force Criteria.

F. Ruschitzka, W. Berger, A. Medeiros-Domingo, 2020, Circulation. Genomic and precision medicine.

Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes

S. Feil, W. Berger, C. Gerth-Kahlert, 2021, Genes.

Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1.

R. Reinhardt, A. Beck, R. Roepman, 1996, Human molecular genetics.

Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes

W. Berger, G. Russo, A. Medeiros-Domingo, 2018, International Journal of Legal Medicine.

A non‐ancestral RPGR missense mutation in families with either recessive or semi‐dominant X‐linked retinitis pigmentosa

D. Sharon, R. Roepman, T. Rosenberg, 2007, American journal of medical genetics. Part A.

RELP-discordance within the human phenylalanine hydroxylase locus

W. Berger, O. Riess, P. Nürnberg, 1989, Human Genetics.

ABCA4 and ROM1: implications for modification of the PRPH2-associated macular dystrophy phenotype.

M. Bach, W. Berger, W. Lagrèze, 2010, Investigative ophthalmology & visual science.

Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasia.

S. Feil, W. Berger, C. Gerth-Kahlert, 2019, Human molecular genetics.

A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO‐1 and UBC9 (Am J Med Genet 136A: 31–37, 2005)

W. Berger, A. Zankl, D. Betts, 2005, American journal of medical genetics. Part A.

Quantitative sequence analysis of FBN1 premature termination codons provides evidence for incomplete NMD in leukocytes

Beat Steinmann, Gábor Mátyás, Marie-Claude Addor, 2009, Human mutation.

Mutation- and tissue-specific alterations of RPGR transcripts.

F. Cremers, W. Berger, E. Glaus, 2010, Investigative ophthalmology & visual science.

Large genomic fibrillin-1 (FBN1) gene deletions provide evidence for true haploinsufficiency in Marfan syndrome

W. Berger, A. Patrignani, I. Magyar, 2007, Human Genetics.

Analysis of sporadic neuroendocrine tumours of the enteropancreatic system by comparative genomic hybridisation

W. Berger, B. Wiedenmann, M. Toliat, 2001, Gut.

Identification and characterization of a novel RPGR isoform in human retina

W. Berger, E. Glaus, J. Neidhardt, 2007, Human mutation.

Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene

W. Berger, E. Boltshauser, D. Bartholdi, 2006, Clinical genetics.

Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.

Peter Nürnberg, S. Feil, W. Berger, 2006, Investigative ophthalmology & visual science.

Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt

A. Rump, I. Glass, W. Berger, 2016, Journal of Medical Genetics.

Mutations in the candidate gene for Norrie disease.

T. Meitinger, M. Warburg, A. Meindl, 1992, Human molecular genetics.

Retinoschisislike alterations in the mouse eye caused by gene targeting of the Norrie disease gene.

E Zrenner, E. Zrenner, W. Berger, 1997, Investigative ophthalmology & visual science.

Mutations in the X-linked RP2 gene cause intracellular misrouting and loss of the protein.

S. Lenzner, W. Berger, U. Schwahn, 2001, Human molecular genetics.

Polar body diagnosis (PBD): an alternative and supplement to preimplantation diagnosis for single embryo transfer

W. Berger, A. Rauch, B. Oneda, 2015 .

Genotype–phenotype spectrum in isolated and syndromic nanophthalmos

S. Feil, W. Berger, K. Fasler, 2020, Acta ophthalmologica.

DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements

J. Ramser, R. Kirschner, F. Cremers, 2001, Human Genetics.

The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors.

R. Roepman, F. Cremers, H. Ropers, 2000, Human molecular genetics.

Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing

B. Lorenz, T. Rosenberg, S. Feil, 2008, Molecular vision.

Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2).

T. Rosenberg, S. Feil, W. Berger, 1999, Ophthalmic genetics.

Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction

L. Vissers, I. Fajardy, D. Sharon, 2023, HGG advances.

Impact of Loading Phase, Initial Response and CFH Genotype on the Long-Term Outcome of Treatment for Neovascular Age-Related Macular Degeneration

W. Berger, M. Menghini, F. Sutter, 2012, PloS one.

Genetic association with response to intravitreal ranibizumab in patients with neovascular AMD.

W. Berger, S. Michels, C. Schindler, 2011, Investigative ophthalmology & visual science.

Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.

W. Berger, J. Neidhardt, D. Barthelmes, 2006, Investigative ophthalmology & visual science.

RPGR mutations might cause reduced orientation of respiratory cilia

E. Haan, H. Omran, W. Berger, 2013, Pediatric pulmonology.

Degenerative Aortic Valve Stenosis, but not Coronary Disease, Is Associated With Shorter Telomere Length in the Elderly

A. Akhmedov, F. Eberli, T. Lüscher, 2006, Arteriosclerosis, thrombosis, and vascular biology.

Localizing the RPGR protein along the cilium: a new method to determine efficacies to treat RPGR mutations

W. Berger, E. Glaus, J. Neidhardt, 2015, Gene Therapy.

Absence of Goniodysgenesis in Patients with Chromosome 13Q Microdeletion-Related Microcoria.

W. Berger, P. Nürnberg, C. Gerth-Kahlert, 2018, Ophthalmology. Glaucoma.

Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome

W. Berger, G. Nürnberg, P. Nürnberg, 2014, PloS one.

Novel VCAN mutations and evidence for unbalanced alternative splicing in the pathogenesis of Wagner syndrome

W. Berger, A. Fry, J. Zech, 2012, European Journal of Human Genetics.

Lack of paraoxonase 1 alters phospholipid composition, but not morphology and function of the mouse retina.

C. Grimm, T. Hornemann, A. von Eckardstein, 2014, Investigative ophthalmology & visual science.

Regulation of ABCA1 by AMD-Associated Genetic Variants and Hypoxia in iPSC-RPE

C. Grimm, A. D. den Hollander, W. Berger, 2022, International journal of molecular sciences.

Regulatory regions of the paraoxonase 1 (PON1) gene are associated with neovascular age-related macular degeneration (AMD)

C. Grimm, W. Berger, M. Menghini, 2012, AGE.

The Expression of Decidual Protein Induced by Progesterone (DEPP) Is Controlled by Three Distal Consensus Hypoxia Responsive Element (HRE) in Hypoxic Retinal Epithelial Cells

C. Grimm, M. Samardzija, W. Berger, 2020, Genes.

Overexpression of RPGR Leads to Male Infertility in Mice Due to Defects in Flagellar Assembly1

C. Grimm, S. Feil, W. Berger, 2008, Biology of reproduction.

The timing of auditory sensory deficits in Norrie disease has implications for therapeutic intervention

K. Steel, M. Bitner-Glindzicz, D. Jagger, 2022, JCI insight.

Multimodal Imaging of Autosomal Dominant Drusen

W. Berger, S. Michels, S. Zweifel, 2012, Klinische Monatsblätter für Augenheilkunde.

Differential gene expression in Ndph-knockout mice in retinal development.

S. Feil, W. Berger, U. Luhmann, 2009, Investigative ophthalmology & visual science.

Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease

H. Rehm, M. C. Brown, D. Corey, 2002, The Journal of Neuroscience.

Alterations of the 5'untranslated region of SLC16A12 lead to age-related cataract.

W. Berger, S. Bhattacharya, A. Moore, 2010, Investigative ophthalmology & visual science.

Alterations of the 5 ’ untranslated leader region of SLC 16 A 12 lead to age-related cataract

W. Berger, S. Bhattacharya, A. Moore, 2010 .

Fetal loss in homozygous mutant Norrie disease mice: A new role of Norrin in reproduction

W. Berger, U. Luhmann, W. Shi, 2005, Genesis.

Regulatory regions of the paraoxonase 1 (PON1) gene are associated with neovascular age-related macular degeneration (AMD)

C. Grimm, W. Berger, M. Menghini, 2013, AGE.

Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis.

A. D. den Hollander, C. Westall, F. Cremers, 2016, Investigative ophthalmology & visual science.

Cone versus rod disease in a mutant Rpgr mouse caused by different genetic backgrounds.

K. Knobeloch, S. Feil, W. Berger, 2010, Investigative ophthalmology & visual science.

Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases

W. Berger, A. Medeiros-Domingo, C. Haas, 2016, International Journal of Legal Medicine.

Erratum to: Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases

W. Berger, A. Medeiros-Domingo, C. Haas, 2016, International Journal of Legal Medicine.

Functional Characterization of an In-Frame Deletion in the Basic Domain of the Retinal Transcription Factor ATOH7

S. Feil, W. Berger, D. Haenni, 2022, International journal of molecular sciences.

The Norrie Disease Gene: Positional Cloning, Mutation Analysis and Protein Homologies

T. Meitinger, A. Meindl, H. Ropers, 1993 .

Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa

S. Feil, W. Berger, C. Gerth-Kahlert, 2023, Genes.

An animal model for Norrie disease (ND): gene targeting of the mouse ND gene.

H. Ropers, W. Berger, H. Hameister, 1996, Human molecular genetics.

Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB)

F. Cremers, H. Ropers, W. Berger, 2004, Human Genetics.

A potential mouse model for the erosive vitreoretinopathy of Wagner disease

W. Berger, K. Rüther, M. Dours-Zimmermann, 2016 .

Global gene expression analysis in a mouse model for Norrie disease: late involvement of photoreceptor cells.

S. Lenzner, S. Feil, H. Ropers, 2002, Investigative ophthalmology & visual science.

Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retina

S. Beck, Marina Garcia Garrido, V. Sothilingam, 2018, Scientific Reports.

Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneity.

J. Ramser, A. Meindl, P. Lichtner, 2001, International journal of molecular medicine.

Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1

E. Zrenner, A. Meindl, W. Berger, 2000, Human Genetics.

Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome

T. Meitinger, A. Meindl, F. Cremers, 1992, Human Genetics.

Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes.

A H van Gennip, D. Murphy, H. Brunner, 1996, The Journal of clinical investigation.

Voltage-dependent ion channels in the mouse RPE: Comparison with Norrie disease mice

S. Lenzner, W. Berger, R. Rosenthal, 2006, Vision Research.