W Rosenkranz

NewYork–Presbyterian Brooklyn Methodist Hospital — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

17h-index952citations105works0.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(16), Prenatal Screening and Diagnostics(11), Chromosomal and Genetic Variations(7), Cystic Fibrosis Research Advances(7), Genetic Mapping and Diversity in Plants and Animals(5)

Publications101 total

Pick Me: Point of care ultrasound diagnosis of an inferior shoulder dislocation
Visual Journal of Emergency Medicine·2025
A new frameshift mutation 460delG in exon 4 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
Human Mutation·1996
A new frameshift mutation 460delG in exon 4 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
Human Mutation·1996
Molecular and clinical findings in Austrian cystic fibrosis patients with mutations in exon 11 of the CFTR gene.
PubMed·1995· 2 cited
A sporadic form of hereditary neuropathy with liability to pressure palsies
Neurology·1994· 27 cited
A New Missense Mutation G1249E in Exon 20 of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene
Human Heredity·1994· 3 cited
A New Missense Mutation G126D in Exon 4 of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene
Human Heredity·1994· 17 cited
A cystic fibrosis patient with ΔF508, G542X and a deletion at the D7S8 locus
Human Mutation·1994· 5 cited
Qualitative Analyse von fetalen Bewegungsmustern bei Fehlbildungen
Gyn�kologisch-geburtshilfliche Rundschau·1994
[Molecular genetic diagnosis of Wiskott-Aldrich syndrome].
PubMed·1993
Clinical and Molecular Analysis of Five(Inv) Dup(15) Patients
European Journal of Human Genetics·1993· 174 cited
Identification of a new splice site mutation (3849 +1G←A) in the intron 19 of the CFTR gene
Human Molecular Genetics·1993· 1 cited
Microdissection of a human marker chromosome reveals its origin and a new family of centromeric repetitive DNA
Human Molecular Genetics·1992· 28 cited
Frequency of ?F508 and haplotype association in Austrian cystic fibrosis families
Human Genetics·1992· 7 cited
Localization of genes and anonymous DNA probes on the short arm of Chromosome 7
Mammalian Genome·1992· 6 cited
Announcement
Human Heredity·1992Open Access
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)
Human Molecular Genetics·1992· 60 cited
Uniparental Origin of Sex Chromosome Polysomies
Human Heredity·1992· 26 cited
A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p
Genomics·1991· 17 cited
A Taql RFLP detected by the probe TN157 (D7S145) at the human chromosome region 7p13 – 14.2
Nucleic Acids Research·1991· 3 citedOpen Access
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Frequent Co-authors

Gerda Vistorin(5), Roswitha Gamperl(5), Klaus Wagner(5), Rudolf Rigler(5), Ignaz Greil(4), A. Behmel(3), Peter M. Kroisel(3), W.‐U. Müller(3), Franz Binkert(2), Albert Schinzel(2), Klaus W. Wagner(2), H. Hofmann(2), H Zierler(2), PM Kroisel(2), Stefanie U. Hölzer(2), Petra Schneditz(2), Peter M. Kroisel(2), M Zach(2), Wendy P. Robinson(1), Ramon Giné(1)