I. Hansmann

发表

The human gene for oxytocin-neurophysin I (OXT) is physically mapped to chromosome 20p13 by in situ hybridization.

J. Battey, V. Rao, C. Löffler, 1992, Cytogenetics and cell genetics.

Renal failure and hypertension in Alagille syndrome with a novel JAG1 mutation.

F. Thaiss, R. Stahl, S. Harendza, 2005, Journal of nephrology.

Inheritance of a meiosis I error expressed in mouse oocytes and modulated by a maternal factor.

E. Hummler, F. Beermann, I. Hansmann, 1987, Genetical research.

Cystatin C (CST3), the candidate gene for hereditary cystatin C amyloid angiopathy (HCCAA), and other members of the cystatin gene family are clustered on chromosome 20p11.2.

S. Schnittger, M. Abrahamson, V. Rao, 1993, Genomics.

Nondisjunction by failures in the molecular control of oocyte maturation.

I. Hansmann, B. Pabst, 1992, Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft.

The RBE of 30 kV X-rays for the induction of dicentric chromosomes in human lymphocytes

D. Harder, I. Hansmann, R. Virsik, 1977, Radiation and environmental biophysics.

Control of meiosis by somatic cells in mice: inheritance of the meiosis I error 'diploidy' and nonexpression in sensitive NMRI/Han oocytes ovulated from chimeras.

I. Hansmann, J. Jenderny, I. Bartels, 1984, Cell differentiation.

Mechanisms of nondisjunction: facts and perspectives.

E. Hummler, F. Beermann, I. Hansmann, 1985, Basic life sciences.

Familial Prader-Willi syndrome with apparently normal chromosomes.

D. Ledbetter, I. Hansmann, M. Lubinsky, 1987, American journal of medical genetics.

Characterization and regional mapping of new anonymous chromosome 20-specific DNA markers isolated from a flow-sorted DNA library.

K. Grzeschik, S. Schnittger, I. Hansmann, 1991, Genomics.

Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24.

I. Hansmann, A. Midro, C. Färber, 2001, Genomics.

High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.

E. Zackai, N. Spinner, S. Schuffenhauer, 1993, Journal of medical genetics.

Parental mosaicism of JAG1 mutations in families with Alagille syndrome

J. Fryns, A. Bankier, A. Röpke, 2001, European Journal of Human Genetics.

Mapping of the ribophorin II (RPN II) gene to human chromosome 20q12–q13.1 by in-situ hybridization

V. Rao, C. Löffler, I. Hansmann, 1991, Human Genetics.

G protein Gs alpha (GNAS 1), the probable candidate gene for Albright hereditary osteodystrophy, is assigned to human chromosome 20q12-q13.2.

S. Schnittger, V. Rao, I. Hansmann, 1991, Genomics.

Transgenic mouse--an in vivo system for detection of aneugens.

J. Vijg, A. Natarajan, E. Hummler, 1990, Progress in clinical and biological research.

Twelve novel JAG1 gene mutations in polish Alagille syndrome patients

I. Hansmann, D. Jurkiewicz, E. Popowska, 2005, Human mutation.

Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting the JAG1 gene.

P. Stankiewicz, I. Hansmann, M. Krajewska-Walasek, 2001, American journal of medical genetics.

Gene structure of semenogelin I and II. The predominant proteins in human semen are encoded by two homologous genes on chromosome 20.

H. Lilja, N. Spurr, C. Lazure, 1992, The Journal of biological chemistry.

The gene for the novel vasoactive peptide endothelin 3 (EDN3) is localized to human chromosome 20q13.2-qter.

V. Rao, C. Löffler, I. Hansmann, 1991, Genomics.

Prenatal diagnosis of genetic disease by chorionic villi sampling

I. Hansmann, I. Bartels, Ingo Hansmann, 1986, Indian journal of pediatrics.

A genetic map of chromosome 20q12-q13.1: multiple highly polymorphic microsatellite and RFLP markers linked to the maturity-onset diabetes of the young (MODY) locus.

P. N. Rao, T. Keith, I. Hansmann, 1993, American journal of human genetics.

Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus.

P. Stankiewicz, G. Rappold, I. Hansmann, 2001, American journal of medical genetics.

A new polymorphic DNA probe pS43 derived from a flow sorted library is assigned to human chromosome 20q13

S. Schnittger, F. Beermann, I. Hansmann, 1989, Human Genetics.

Biochemical and therapeutical studies in a case of atrophia gyrata

I. Hansmann, W. Behrens-Baumann, U. Langenbeck, 2005, Graefe's Archive for Clinical and Experimental Ophthalmology.

Chromosome segregation at meiosis I in female T(2;4)1Gö/+ mice: no evidence for a decreased crossover frequency with maternal age

F. Beermann, I. Hansmann, I. Bartels, 2004, Chromosoma.

Structural variability of human chromosome 9 in relation to its evolution

I. Hansmann, 1976, Human Genetics.

A subtelocentric chromosome 9 in a dysplastic 18-year-old boy with dissociated mental development

I. Hansmann, J. Keute, 1975, Humangenetik.

Crossing-over during human spermatogenesis visualized cytologically

I. Hansmann, T. Grimm, M. Geisler, 2004, Human Genetics.

Cri‐du‐chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatin

I. Hansmann, T. Grimm, H. Gebauer, 1978, Clinical genetics.

Aneuploidy in man and mechanisms of nondisjunction inferred from studying Djungarian hamster oocytes

E. Hummler, F. Beermann, I. Hansmann, 1990 .

The dup(3q) syndrome: report of eight cases and review of the literature.

J. Opitz, L. Meisner, I. Hansmann, 1981, American journal of medical genetics.

High susceptibility for diploidy in ovulated oocytes from XO mice

F. Beermann, I. Hansmann, U. Franke, 1986, Human Genetics.

Absence of specific luteinizing hormone-releasing hormone (LHRH) receptors in the ovaries of Djungarian hamsters (Phodopus sungorus).

I. Hansmann, F. Theuring, U. Uçer, 1987, Biology of reproduction.

Comparative Mutagenicity of Procarbazine (Natulan)

I. Hansmann, 1981 .

Molecular structure and chromosomal mapping of the human homolog of the agouti gene.

W. Wilkison, J. G. Powell, C. Löffler, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Reciprocal or nonreciprocal human chromosome translocations?

I. Hansmann, T. Grimm, C. Wiedeking, 1977, Human Genetics.

Impaired gene activity for 18S and 28S rRNA in early embryonic development of mouse parthenogenones

I. Hansmann, T. Grimm, J. Gebauer, 1978, Nature.

A sterile male with 45,X0 and a Y;22 translocation

S. Schnittger, J. Schmidtke, I. Hansmann, 1991, Human Genetics.

The 9p24.3 Breakpoint of a Constitutional t(6;9)(p12;p24) in a Patient with Chronic Lymphocytic Leukemia Maps Close to the Putative Promoter Region of the DMRT2 Gene

J. Rüssel, I. Hansmann, D. Wand, 2009, Cytogenetic and Genome Research.

Bibliography of Ulrich Wolf

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

The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families

A. Robinson, Y. Fukushima, N. Niikawa, 2004, Human Genetics.

Onset of nucleolus organizer activity in early mouse embryogenesis and evidence for its regulation.

I. Hansmann, T. Grimm, J. Gebauer, 1978, Experimental cell research.

H-Y antigen in Turner's syndrome patients with different sex chromosome constitutions

W. Engel, I. Hansmann, B. Klemme, 2004, Human Genetics.

An excess of chromosome 1 breakpoints in male infertility

R. Stallings, C. Lundsteen, Z. Tümer, 2004, European Journal of Human Genetics.

A family case of fertile human 45,X,psu dic(15;Y) males

W. Schempp, P. M. Gopinath, I. Hansmann, 2006, Cytogenetic and Genome Research.

Phenotypic variability in Hey2 −/− mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome

A. Fischer, M. Gessler, I. Hansmann, 2004, Mammalian Genome.

Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family

E. Mariman, B. Hamel, I. Hansmann, 1995, Human Genetics.

Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH).

P Gruss, R. Balling, P. Gruss, 1992, Genomics.

Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expression.

P. Stankiewicz, I. Hansmann, H. Thiele, 2001, American journal of medical genetics.

Assignment1 of SUPV3L1 to human chromosome band 10q22.1 by in situ hybridization

P. Stankiewicz, P. Golik, I. Hansmann, 1999, Cytogenetic and Genome Research.

20p12.3 microdeletion predisposes to Wolff–Parkinson–White syndrome with variable neurocognitive deficits

Z. Ou, P. Stankiewicz, A. C. Chinault, 2008, Journal of Medical Genetics.

Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome

A. Röpke, I. Hansmann, A. Kujat, 2003, Human mutation.

Parental mosaicism of JAG1 mutations in families with Alagille syndrome

J. Fryns, A. Bankier, A. Röpke, 2001, European Journal of Human Genetics.

Report of the First International Workshop on Human Chromosome 20 Mapping 1993.

J. Weissenbach, D. Bowden, T. Keith, 1994, Cytogenetics and cell genetics.

Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation

P. Stankiewicz, J. Lupski, T. Liehr, 2006, American journal of medical genetics. Part A.

Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVS.

H. Rehder, C. Waldenmaier, B. Zoll, 1992, American journal of medical genetics.

Duplication of Xq26.2–q27.1, including SOX3, in a mother and daughter with short stature and dyslalia

P. Stankiewicz, J. Lupski, S. Bartel-Friedrich, 2005, American journal of medical genetics. Part A.

High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 gene.

H. Kehrer-Sawatzki, L. Kluwe, K. Wimmer, 2004, American journal of human genetics.

Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)

S. Schnittger, F. Beermann, I. Hansmann, 1989, Human Genetics.

Maternal UPD 20 in a hyperactive child with severe growth retardation

G. Senger, I. Hansmann, I. Chudoba, 1999, European Journal of Human Genetics.

Cytogenetic analysis of early human abortuses after preparation of chromosomes directly from chorionic villi

I. Hansmann, I. Bartels, I. Schübbe, 1986, Human Genetics.

Silver-Russell syndrome and cystic fibrosis associated with maternal uniparental disomy 7.

I. Hansmann, U. Hehr, M. Hagemann, 2000, American journal of medical genetics.

Genomic structure of karyopherin α2 (KPNA2) within a low-copy repeat on chromosome 17q23-q24 and mutation analysis in patients with Russell-Silver syndrome

I. Hansmann, S. Dörr, M. Schlicker, 2001, Human Genetics.

Low doses of X-rays decrease the risk of diploidy in mouse oocytes.

I. Hansmann, J. Jenderny, H. Probeck, 1983, Mutation research.

Follicular maturation, luteinization and first meiotic division in oocytes after inhibiting mitochondrial function in mice with chloramphenicol.

F. Beermann, I. Hansmann, 1986, Mutation research.

Incidence of nondisjunction in mouse oocytes.

I. Hansmann, E. El-Nahass, 1979, Cytogenetics and cell genetics.

Detection of nondisjunction in mammals.

I. Hansmann, H. Probeck, 1979, Environmental health perspectives.

Induced chromosomal aberrations in pronuclei, 2-cell stages and morulae of mice.

I. Hansmann, 1973, Mutation research.

Chromosomal imbalance in ovulated oocytes from Syrian hamsters (Mesocricetus auratus) and Chinese hamsters (Cricetulus griseus).

I. Hansmann, H. Probeck, 1979, Cytogenetics and cell genetics.

Chromosome anomalies in mouse oocytes after irradiation

I. Hansmann, W. Reichert, G. Röhrborn, 1975, Human Genetics.

Chromosome aberrations in metaphase II oocytes of Chinese hamster (Cricetulus griseus). I. The sensitivity of the pre-ovulatory phase to triaziquone.

I. Hansmann, G. Röhrborn, J. Neher, 1974, Mutation research.

Chromosome aberrations in metaphase II-oocytes. Stage sensitivity in the mouse oogenesis to amethopterin and cyclophosphamide.

I. Hansmann, 1974, Mutation research.

Genomic organization and expression pattern of scapinin (PHACTR3) in mouse and human

I. Hansmann, S. Worch, D. Schlote, 2006, Cytogenetic and Genome Research.

Excess of females in chromosomally normal spontaneous abortuses.

I. Hansmann, B. Eiben, I. Bartels, 1990, American journal of medical genetics.

A cytogenetic study directly from chorionic villi of 140 spontaneous abortions

I. Hansmann, B. Eiben, S. Borgmann, 1987, Human Genetics.

Follicular development in immature Djungarian hamsters (Phodopus sungorus) and the influence of exogenous gonadotropins.

I. Hansmann, F. Theuring, 1986, Biology of reproduction.

The predictive value of chorionic villus histology for identifying chromosomally normal and abnormal spontaneous abortions

M. Vogel, I. Hansmann, B. Eiben, 1989, Human Genetics.

Chromosome anomalies in 136 couples with a history of recurrent abortions

I. Hansmann, U. Diedrich, H. Probeck, 2004, Human Genetics.

Chromosome aberrations in preimplantation stages of mice after treatment with triazoquinone

I. Hansmann, G. Röhrborn, 1973, Humangenetik.

Pattern and frequency of nondisjunction in oocytes from the Djungarian hamster are determined by the stage of first meiotic spindle inhibition

E. Hummler, I. Hansmann, 1988, Chromosoma.

Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq.

A. Clarke, L. Edström, M. Anvret, 1998, Journal of medical genetics.

Developmental pathogenesis of chromosome disorders: report on two newly recognized signs of Down syndrome.

I. Hansmann, U. Langenbeck, E. Blum, 1984, American journal of medical genetics.

The genetic significance of accessory bisatellited marker chromosomes

M. Djalali, M. Wolf, I. Hansmann, 2004, Human Genetics.

The genetic basis of non-disjunction: Increased incidence of hyperploidy in oocytes from F1 hybrid mice

I. Hansmann, J. Jenderny, 2004, Human Genetics.

Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia.

J. P. Meza-Espinoza, I. Hansmann, M. Gutiérrez-Angulo, 2002, Cancer genetics and cytogenetics.

Short communication Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia

I. Hansmann, 2002 .

Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature.

I. Hansmann, U. Dutta, D. Schlote, 2015, European journal of medical genetics.

Chromosomal mosaicism of trisomy 7 restricted to chorionic villi.

I. Hansmann, I. Bartels, R. Rauskolb, 1986, American journal of medical genetics.

Fanconi's anaemia developing erythroleukaemia.

G. Prindull, I. Hansmann, E. Jentsch, 2009, Scandinavian journal of haematology.

Aspects of Nondisjunction

I. Hansmann, 1984 .

The gene for bone morphogenetic protein 2A (BMP2A) is localized to human chromosome 20pl2 by radioactive and nonradioactive in situ hybridization

J. Wozney, V. Rao, C. Löffler, 1992, Human Genetics.

Association of a specific haplotype across the genes MMP1 and MMP3 with radiographic joint destruction in rheumatoid arthritis

U. Wagner, B. Müller-Myhsok, R. Rau, 2004, Arthritis research & therapy.

Prenatal Diagnosis and Fetopathological Findings in a Fetus with Ring Chromosome 18

H. Rehder, B. Zoll, I. Hansmann, 1998, Fetal Diagnosis and Therapy.

Preferential nondisjunction of specific bivalents in oocytes from Djungarian hamsters (Phodopus sungorus) following colchicine treatment.

E. Hummler, I. Hansmann, 1985, Cytogenetics and cell genetics.

A female with XO/XY mosaicism and partial trisomy 9p.

M. Schmid, J. Schmidtke, I. Hansmann, 1981, Journal of Medical Genetics.

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

Uwe Claussen, Thomas Liehr, T. Liehr, 2002, European Journal of Human Genetics.

Down syndrome at birth not detected by first-trimester chorionic villus sampling.

B. Zoll, I. Hansmann, I. Bartels, 1989, American journal of medical genetics.

Assignment1 of Karyopherin alpha 1 (KPNA1) to human chromosome band 3q21 by in situ hybridization

I. Hansmann, M. L. Ayala-Madrigal, M. L. Ramírez-Dueńas, 2000, Cytogenetic and Genome Research.

Assignment1 of KPNA4 and KPNB1 encoding karyopherin alpha 4 and beta 1 to human chromosome bands 11q22 and 17q21 respectively, by in situ hybridization

I. Hansmann, M. L. Ayala-Madrigal, M. L. Ramírez-Dueńas, 2000, Cytogenetic and Genome Research.

A familial X-autosome translocation with the breakpoint in the “critical region”

I. Hansmann, U. Diedrich, 2004, Human Genetics.

Maternal modulation of the inheritable meiosis I error Dipl I in mouse oocytes is associated with the type of mitochondrial DNA

E. Hummler, F. Beermann, I. Hansmann, 1988, Human Genetics.

Clustering of chromosomal aneuploidy and tracing of nondisjunction in man.

I. Hansmann, 1979, Environmental health perspectives.

X-ray induced reciprocal translocations and dicentrics in human G0 lymphocytes.

I. Hansmann, R. Virsik, U. Meyding, 1983, International journal of radiation biology and related studies in physics, chemistry, and medicine.

Meiotic nondisjunction in oocytes from aged Djungarian hamsters correlates with an alteration in meiosis rate but not in univalent formation

E. Hummler, I. Hansmann, F. Theuring, 1987, Human Genetics.

Cytogenetic investigation of 103 patients with primary or secondary amenorrhea

I. Hansmann, B. Hinney, O. Opitz, 2004, Human Genetics.

Sex reversal in the mouse

I. Hansmann, 1982, Cell.

Induced chromosome aberrations in unfertilized oocytes of mice

I. Hansmann, G. Röhrborn, 2004, Humangenetik.

Oral contraceptives and chromosome segregation in oocytes of mice.

I. Hansmann, G. Röhrborn, 1974, Mutation research.

On the origin of the supernumerary chromosome in autosomal trisomies — with special reference to Down's syndrome

I. Hansmann, U. Langenbeck, B. Hinney, 1976, Human Genetics.

Phenotype–genotype correlations in patients with Marinesco–Sjögren syndrome

J. Graham, W. Wilcox, I. Hansmann, 2014, Clinical genetics.

The predictive value of dermatoglyphic anomalies in the diagnosis of fra(X)-positive Martin-Bell syndrome (MBS)

I. Hansmann, I. Varga, U. Langenbeck, 1988, American journal of medical genetics.

Nondisjunction and chromosome breakage in mouse oocytes after various X-ray doses

I. Hansmann, J. Jenderny, H. Probeck, 1982, Human Genetics.

The gene for the amyloid precursor-like protein APLP2 is assigned to human chromosome 11q23-q25.

J. Hanes, J. Klaudiny, C. Löffler, 1994, Genomics.

The induction of non-disjunction by irradiation in mammalian oogenesis and spermatogenesis.

I. Hansmann, H. Probeck, 1979, Mutation research.

Induced chromosome aberrations in early embryogenesis of mice

I. Hansmann, G. Röhrborn, O. Kühn, 2004, Humangenetik.

Neuropathology of Seckel syndrome in fetal stage with evidence of intrauterine developmental retardation

I. Hansmann, A. Hori, S. Eber, 2004, Acta Neuropathologica.

Partial deletion of 4p in fetal cells not present in chorionic villi

I. Hansmann, B. Eiben, M. Leipoldt, 1988, Clinical genetics.

RAPID CYTOGENETIC DIAGNOSIS OF EARLY SPONTANEOUS ABORTIONS

I. Hansmann, B. Eiben, S. Borgmann, 1986, The Lancet.

2. A Multilocus DNA Fingerprint with Built-in Security Devices

M. Krawczak, J. Schmidtke, I. Hansmann, 1994, Medicine, science, and the law.

Report of the First International Workshop on Human Chromosome 20 Mapping 1993

J. Weissenbach, T. Keith, I. Hansmann, 1994 .

The gene for receptor-linked protein-tyrosine-phosphatase (PTPA) is assigned to human chromosome 20p12-pter by in situ hybridization (ISH and FISH).

J. Schlessinger, J. Sap, V. Rao, 1992, Genomics.

Familial mosaicism of del(Y) and inv del(Y)

P. Yen, W. Schempp, I. Hansmann, 2001, Cytogenetic and Genome Research.

Aneuploidy in mouse fetuses after paternal exposure to X rays

I. Hansmann, J. Jenderny, J. Schäfer, 1979, Nature.

PRENATAL DIAGNOSIS OF MOST COMMON MEDITERRANEAN β-THALASSAEMIA MUTANTS

M. Pirastu, A. Cao, I. Hansmann, 1986, The Lancet.

Stage sensitivity in the oogenesis of mice

I. Hansmann, G. Röhrborn, 1973 .

Gene symbol: JAG1. Disease: tetralogy of Fallot.

A. Caliebe, I. Hansmann, D. Kotzot, 2006, Human genetics.

A male with a monocentric Yq isochromosome and presence of a Yp-specific DNA sequence

M. Schmid, J. Schmidtke, I. Hansmann, 2004, Human Genetics.