J
Jean Weissenbach
Researcher at Université Paris-Saclay
Publications - 56
Citations - 35232
Jean Weissenbach is an academic researcher from Université Paris-Saclay. The author has contributed to research in topics: Genome & Locus (genetics). The author has an hindex of 34, co-authored 56 publications receiving 32457 citations. Previous affiliations of Jean Weissenbach include University of Évry Val d'Essonne & Commissariat à l'énergie atomique et aux énergies alternatives.
Papers
More filters
Journal Article
A locus for Fanconi anemia on 16q determined by homozygosity mapping.
M. Gschwend,O. Levran,Leonid Kruglyak,Koustubh Ranade,Peter C. Verlander,S. Shen,Sabine Fauré,Jean Weissenbach,C. Altay,Eric S. Lander,Arleen D. Auerbach,David Botstein +11 more
TL;DR: The results of a genomewide scan using homozygosity mapping to identify genes causing Fanconi anemia, a genetically heterogeneous recessive disorder, find strong evidence of genetic heterogeneity and demonstrate the strong effect of marker allele frequencies on LOD scores obtained in hom chromosome mapping.
Journal ArticleDOI
A fourth locus for Autosomal Dominant Hypercholesterolemia maps at 16q22.1
Alice Marques-Pinheiro,M. Marduel,Jean-Pierre Rabès,Martine Devillers,Ludovic Villéger,Delphine Allard,Jean Weissenbach,Maryse Guerin,Yassine Zair,D. Erlich,Claudine Junien,Arnold Munnich,Michel Krempf,Marianne Abifadel,Marianne Abifadel,Jean-Philippe Jais,Catherine Boileau,Mathilde Varret +17 more
TL;DR: The results show the existence of other ADH genes as nine families were neither linked to LDLR, APOB, and PCSK9 genes nor to the new HCHOLA4 locus.
Journal ArticleDOI
No evidence of genetic heterogeneity in dominant optic atrophy.
Dominique Bonneau,Eric H Souied,Sylvie Gerber,Jean-Michel Rozet,E D'Haens,Hubert Journel,Ghislaine Plessis,Jean Weissenbach,Arnold Munnich,J. C. Kaplan +9 more
TL;DR: The present study provides three new markers closely linked to the disease gene for future genetic studies in OPA by showing close linkage of the disease locus to three recently reported microsatellite DNA markers in the interval defined by loci D3S1314 andD3S1265 in four French families.
The sequence of rice chromosomes 11 and 12 rich in disease resistance genes and recent gene duplicationsRice Chromosomes 11 and 12 Sequencing Consortia (RCSC)BMC Biol2005320126116516188032
Nathalie Choisne,Nadia Demange,Gisela Orjeda,Sylvie Samain,Angélique D'Hont,Laurence Cattolico,Eric Pelletier,Arnaud Couloux,Béatrice Segurens,Patrick Wincker,Claude Scarpelli,Jean Weissenbach,Marcel Salanoubat,Francis Quetier,Singh Nk,Trilochan Mohapatra,Tilak Raj Sharma,Kishor Gaikwad,Alok Singh,Vivek Dalal,Subodh K. Srivastava,Anupam Dixit,Ajit K. Pal,Ghazi Ia,Mahavir Yadav,A. Pandit,Atul Bhargava,K. Sureshbabu,R. Dixit,Harvinder Singh,Swain Sc,S. Pal,M. Ragiba,Pradeep K. Singh,Vibha Singhal,S. D. Mendiratta,Kamlesh Batra,Saurabh Raghuvanshi,Amitabh Mohanty,Bharti Ak,Anupama Gaur,Vipin Gupta,Dibyendu Kumar,Ravi Vydianathan,Shubha Vij,Anita Kapur,Paramjit Khurana,Sulabha Sharma,Khurana Jp,Tyagi Ak,Yuan Qp,Shu Ouyang,Jia Liu,Wei Zhu,Wang Ah,Lin Hn,John P. Hamilton,Brian J. Haas,Jennifer R. Wortman,Jones Km,Mary Kim,Larry Overton,Tamara Tsitrin,Douglas Fadrosh,Jayati Bera,Bruce Weaver,Jin Sh,Shivani Johri,Matt Reardon,Hue Vuong,Luke J. Tallon,S. Van Aken,Matthew R. Lewis,T. Utterback,Tamara Feldblyum,Victoria Zismann,Stacey E. Iobst,Joseph Hsiao,A. R. de Vazeille,Steven L. Salzberg,Owen White,Claire M. Fraser,Buell Cr,Yeisoo Yu,Teri Rambo,Jennifer Currie,Kristi Collura,Kim Hr,D. Stum,Wang Wm,Dave Kudrna,Christopher Mueller,Wing Ra,Melissa Kramer,Lori Spiegel,Lidia Nascimento,R. Preston,Theresa Zutavern,Lance E. Palmer,A. O'Shaughnessy +99 more
TL;DR: In this article, the complete sequences of two rice chromosomes, 11 and 12, were determined and analyzed based on a set of overlapping clones, and a total of 5,993 non-transposable element related genes are present on these chromosomes.
Journal ArticleDOI
Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity.
M Medhioub,Dorra Cherif,F Benessy,Flora Silbermann,Marie-Claire Gubler,D. Le Paslier,O. Cohen,Jean Weissenbach,Jacques S. Beckmann,Corinne Antignac +9 more
TL;DR: Haplotype analyses show unequivocally that four NPH families are not linked to the chromosome 2 markers, although there are no clinical or pathological features discernible in these families that could separate them from the families linked toThe chromosome 2 NPH locus (NPH1).