B
Beatrice Renault
Researcher at Albert Einstein College of Medicine
Publications - 18
Citations - 2385
Beatrice Renault is an academic researcher from Albert Einstein College of Medicine. The author has contributed to research in topics: Gene mapping & Contig. The author has an hindex of 13, co-authored 18 publications receiving 2326 citations. Previous affiliations of Beatrice Renault include Leiden University & Yeshiva University.
Papers
More filters
Journal ArticleDOI
Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.
Craig T. Basson,D. R. Bachinsky,R. C. Lin,Tatjana Levi,Jacob A. Elkins,Johanna Soults,David Grayzel,Elena Kroumpouzou,Thomas A. Traill,Janine M. LeBlanc-Straceski,Janine M. LeBlanc-Straceski,Beatrice Renault,Raju Kucherlapati,Jonathan G. Seidman,Christine E. Seidman +14 more
TL;DR: It is concluded that TBX5 is critical for limb and heart development and suggest that haploinsufficiency ofTBX5 causes Holt-Oram syndrome.
Journal ArticleDOI
A targeted chain-termination mutation in the mouse Apc gene results in multiple intestinal tumors
Riccardo Fodde,Winfried Edelmann,Kan Yang,C. van Leeuwen,C Carlson,Beatrice Renault,Beatrice Renault,Cor Breukel,E Alt,Martin Lipkin,P M Khan +10 more
TL;DR: The results indicate that the Apc gene modification is a critical event in the initiation of intestinal tumor formation and results in an autosomal dominant predisposition toward development of spontaneous colonic and intestinal tumors in mice.
Journal ArticleDOI
Linkage of Asthma and Total Serum IgE Concentration to Markers on Chromosome 12q: Evidence From Afro-Caribbean and Caucasian Populations
Kathleen C. Barnes,John D. Neely,David L. Duffy,Linda R. Freidhoff,Daniel R. Breazeale,Carsten Schou,Raana P. Naidu,Paul N. Levett,Beatrice Renault,Raju Kucherlapati,Sebastiano Iozzino,Eva Ehrlich,Terri H. Beaty,David G. Marsh +13 more
TL;DR: Findings suggest that the 12q15-q24.1 region may contain a gene(s) controlling asthma and the associated "high total IgE" trait.
Journal ArticleDOI
Erratum: Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome (Nature Genetics (1997) 15 (30-35))
Craig T. Basson,D. R. Bachinsky,R. C. Lin,Tatjana Levi,J. A. Elkins,J. Soults,D. Grayzel,E. Kroumpouzou,Thomas A. Traill,J. Leblanc-Straceski,Beatrice Renault,Raju Kucherlapati,Jon G. Seidman,Christine E. Seidman +13 more
TL;DR: The name of the gene TBX5 was unintentionally left out of the title of this report and the authors regret any difficulty this caused.
Journal Article
Type I Transforming Growth Factor β Receptor Maps to 9q22 and Exhibits a Polymorphism and a Rare Variant within a Polyalanine Tract
Boris Pasche,Yan Luo,Pulivarthi H. Rao,Stephen D. Nimer,Ethan Dmitrovsky,Philip Caron,Lucio Luzzatto,Kenneth Offit,Carlos Cordon-Cardo,Beatrice Renault,Jaya M. Satagopan,Vundavalli V. Murty,Joan Massagué,Joan Massagué +13 more
TL;DR: The frequency of TbetaR-I(6A) homozygotes among nontumor and tumor samples obtained from patients with a diagnosis of cancer was higher than that predicted by the Hardy-Weinberg law, and the clinical and biological significance of T betaR- I( 6A)homozygosity needs to be further investigated.