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Jutta Jenderny

Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype.
1993 · J Jenderny, A Caliebe, et al. · Journal of Medical Genetics · 91
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Chromosome aberrations in 450 sperm complements from eight controls and lack of increase after chemotherapy in two patients
1992 · J. Jenderny, M.L. Jacobi, et al. · Human Genetics · 78
Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicism
2009 · Jutta Jenderny, Winfried Schmidt, et al. · European Journal of Pediatrics · 71
Chromosome analysis of human sperm
1987 · J. Jenderny, G. R�hrborn · Human Genetics · 59
Mosaic and complete tetraploidy in live-born infants: two new patients and review of the literature
2010 · Irina Stefanova, Jutta Jenderny, et al. · Clinical Dysmorphology · 52
Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.
1993 · A Meindl, D Hosenfeld, et al. · Journal of Medical Genetics · 49
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Chromosome aberrations in a large series of spontaneous miscarriages in the German population and review of the literature
2014 · Jutta Jenderny · Molecular Cytogenetics · 46
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Detection of a concomitant distal deletion in an inverted duplication of chromosome 3. Is there an overall mechanism for the origin of such duplications/deficiencies?
1998 · Jutta Jenderny, Micaela Poetsch, et al. · European Journal of Human Genetics · 37
Common variable immunodeficiency, impaired neurological development and reduced numbers of T regulatory cells in a 10-year-old boy with a STAT1 gain-of-function mutation
2016 · Robin Kobbe, Manuela Kolster, et al. · Gene · 35
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Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 20
1992 · J. Jenderny, J. Gebauer, et al. · Human Genetics · 34
Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient
1997 · A. Caliebe, S. Waltz, et al. · Clinical Genetics · 29
Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhood
1995 · Jutta Jenderny, Eckhard K�ster, et al. · Human Genetics · 29
Chromosomal abnormalities and sister-chromatid exchange in bone marrow cells of mice and Chinese hamsters after inhalation and intraperitoneal administration: I. diepoxybutane
1987 · R.-A. Walk, J. Jenderny, et al. · Mutation Research/Environmental Mutagenesis and Related Subjects · 27
Interphase cytogenetics on paraffin sections of paediatric extragonadal yolk sac tumours
1996 · J. Jenderny, O. Borchers, et al. · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · 23
Aneuploidy in mouse fetuses after paternal exposure to X rays
1979 · I. HANSMANN, R. ZMARSLY, et al. · Nature · 21
The genetic basis of non-disjunction: Increased incidence of hyperploidy in oocytes from F1 hybrid mice
1983 · I. Hansmann, J. Jenderny · Human Genetics · 20
Low doses of X-rays decrease the risk of diploidy in mouse oocytes
1983 · I. Hansmann, J. Jenderny, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 18
Nondisjunction and chromosome breakage in mouse oocytes after various X-ray doses
1982 · I. Hansmann, J. Jenderny, et al. · Human Genetics · 18
Chromosomal abnormalities and sister-chromatid exchange in bone marrow cells of mice and Chinese hamsters after inhalation and intraperitoneal administration
1988 · J. Jenderny, R.-A. Walk, et al. · Mutation Research/Environmental Mutagenesis and Related Subjects · 14
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
1984 · I. Bartels, J. Jenderny, et al. · Cell Differentiation · 13
Increased Nuchal Translucency, Hydrops fetalis or Hygroma colli
2001 · J. Jenderny, W. Schmidt, et al. · Fetal Diagnosis and Therapy · 12
Sperm chromosome analysis of two males heterozygous for a t(2;17)(q35;p13) and t(3;8)(p13;p21) reciprocal translocation
1992 · J. Jenderny · Human Genetics · 12
Detection of Clonal Aberrations by Cytogenetic Analysis after Different Culture Methods and by FISH in 129 Patients with Chronic Lymphocytic Leukemia
2014 · Jutta Jenderny, Claudia Goldmann, et al. · Cytogenetic and Genome Research · 10
Severe prekallikrein deficiency due to a compound heterozygosis in the KLKB1-gene
2009 · L. Kochhan, P. Heuchel, et al. · Hämostaseologie · 9
Presence of the AZF region in a female with an idic(Y)(q11)
1998 · J. Jenderny, W. Schmidt, et al. · Clinical Genetics · 9
Works count: 39
Citation count: 830
H-index: 18
I10-index: 23
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