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Tatjana Levi

Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome
1997 · Craig T. Basson, David R. Bachinsky, et al. · Nature Genetics · 1,090
Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
1993 · Martin R. Pollak, Edward M. Brown, et al. · Cell · 1,038
Characteristics and Prognostic Implications of Myosin Missense Mutations in Familial Hypertrophic Cardiomyopathy
1992 · Hugh Watkins, Anthony Rosenzweig, et al. · New England Journal of Medicine · 742
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Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1
1989 · John A. Jarcho, William McKenna, et al. · New England Journal of Medicine · 537
Chamber-Specific Cardiac Expression of Tbx5 and Heart Defects in Holt–Oram Syndrome
1999 · Benoit G. Bruneau, Malcolm Logan, et al. · Developmental Biology · 507
Cloning, Expression, and Chromosomal Location of SHH and IHH: Two Human Homologues of the Drosophila Segment Polarity Gene Hedgehog
1995 · Valeria Marigo, Drucilla J. Roberts, et al. · Genomics · 198
Erratum: Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome
1997 · Craig T. Basson, David R. Bachinsky, et al. · Nature Genetics · 114
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Fine-Structure Mapping of the Hereditary Inclusion Body Myopathy Locus
1999 · Iris Eisenberg, Corinna Thiel, et al. · Genomics · 25
Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13
2001 · Iris Eisenberg, Hagit Hochner, et al. · European Journal of Human Genetics · 22
Cloning and characterization of a novel human gene RNF38 encoding a conserved putative protein with a RING finger domain
2002 · Iris Eisenberg, Hagit Hochner, et al. · Biochemical and Biophysical Research Communications · 21
Works count: 10
Citation count: 4,294
H-index: 10
I10-index: 10
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