O
Orna Man
Researcher at Weizmann Institute of Science
Publications - 19
Citations - 5162
Orna Man is an academic researcher from Weizmann Institute of Science. The author has contributed to research in topics: Gene & Olfactory receptor. The author has an hindex of 13, co-authored 19 publications receiving 4899 citations.
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Journal ArticleDOI
Initial sequence of the chimpanzee genome and comparison with the human genome
Tarjei S. Mikkelsen,LaDeana W. Hillier,Evan E. Eichler,Michael C. Zody,David B. Jaffe,Shiaw-Pyng Yang,Wolfgang Enard,Ines Hellmann,Kerstin Lindblad-Toh,Tasha K. Altheide,Nicoletta Archidiacono,Peer Bork,Jonathan Butler,Jean L. Chang,Ze Cheng,Asif T. Chinwalla,Pieter J. de Jong,Kimberley D. Delehaunty,Catrina Fronick,Lucinda L. Fulton,Yoav Gilad,Gustavo Glusman,Sante Gnerre,Tina Graves,Toshiyuki Hayakawa,Karen E. Hayden,Xiaoqiu Huang,Hongkai Ji,W. James Kent,Mary Claire King,Edward J. Kulbokasl,Ming K. Lee,Ge Liu,Carlos López-Otín,Kateryna D. Makova,Orna Man,Elaine R. Mardis,Evan Mauceli,Tracie L. Miner,William E. Nash,Joanne O. Nelson,Svante Pääbo,Nick Patterson,Craig Pohl,Katherine S. Pollard,Kay Prüfer,Xose S. Puente,David Reich,Mariano Rocchi,Kate R. Rosenbloom,Maryellen Ruvolo,Daniel J. Richter,Stephen F. Schaffner,Arian F.A. Smit,Scott M. Smith,Mikita Suyama,James E. Taylor,David Torrents,Eray Tüzün,Ajit Varki,Gloria Velasco,Mario Ventura,John W. Wallis,Michael C. Wendl,Richard K. Wilson,Eric S. Lander,Robert H. Waterston +66 more
TL;DR: It is found that the patterns of evolution in human and chimpanzee protein-coding genes are highly correlated and dominated by the fixation of neutral and slightly deleterious alleles.
Journal ArticleDOI
FoldIndex©: a simple tool to predict whether a given protein sequence is intrinsically unfolded
Jaime Prilusky,Clifford E. Felder,Tzviya Zeev-Ben-Mordehai,Edwin H. Rydberg,Orna Man,Jacques S. Beckmann,Israel Silman,Joel L. Sussman +7 more
TL;DR: An easy-to-use, versatile and freely available graphic web server, FoldIndex© predicts if a given protein sequence is intrinsically unfolded implementing the algorithm of Uversky and co-workers, which is based on the average residue hydrophobicity and net charge of the sequence.
Journal ArticleDOI
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.
Hadas Lahat,Elon Pras,Tsviya Olender,Nili Avidan,Edna Ben-Asher,Orna Man,Etgar Levy-Nissenbaum,Asad Khoury,Avraham Lorber,Boleslaw Goldman,Doron Lancet,Michael Eldar +11 more
TL;DR: A missense mutation in a highly conserved region of the calsequestrin 2 gene (CASQ2) is described as the potential cause of the autosomal recessive form ofatecholamine-induced polymorphic ventricular tachycardia.
Journal ArticleDOI
Human specific loss of olfactory receptor genes
TL;DR: It is found that humans have accumulated mutations that disrupt OR coding regions roughly 4-fold faster than any other species sampled, suggesting a human-specific process of OR gene disruption, likely due to a reduced chemosensory dependence relative to apes.
Journal ArticleDOI
Natural Selection on Genes that Underlie Human Disease Susceptibility
Ran Blekhman,Orna Man,Leslie Herrmann,Adam R. Boyko,Amit Indap,Carolin Kosiol,Carlos Bustamante,Kosuke M. Teshima,Molly Przeworski +8 more
TL;DR: It is found that Mendelian-disease genes appear to be under widespread purifying selection, especially when the disease mutations are dominant (rather than recessive) and the class of genes that influence complex-Disease risk shows little signs of evolutionary conservation.