Results : 1-25/181
Authors:
Edwards, Stephen M.
Kote-Jarai, Zsofia
Meitz, Julia
Hamoudi, Rifat
Hope, Questa
Osin, Peter
Jackson, Rachel
Southgate, Christine
Singh, Rashmi
Faconer, Alison
Dearnaley, David P.
Ardern-Jones, Audrey
Murkin, Annette
Dowe, Anna
Kelly, Jo
Williams, Sue
Oram, Richard
Stevens, Margaret
Teare, Dawn M.
Ponder, A.J. Bruce
Gayther, Simon A.
Cancer Research UK/British Prostate Group UK Familial Prostate Cancer Study Coll
British Association of Urological Surgeons Section of Oncology,
Easton, Doug F.
Eeles, Rosalind A.
Journal: American journal of human genetics
Citation: M. Edwards, Stephen et al., Two Percent of Men with Early-Onset Prostate Cancer Harbor Germline Mutations in the BRCA2 Gene, American journal of human genetics , 72(1), 2003, pp. 1-12
Authors:
Chen, Qui
Reis, Steven E.
Kammerer, Candace M.
McNamara, Dennis M.
Holubkov, Richard
Sharaf, Barry L.
Sopko, George
Pauly, Daniel F.
Bairey Merz, C. Noel
Kamboh, M. Ilyas
WISE Study Group
Journal: American journal of human genetics
Citation: Chen, Qui et al., Association between the Severity of Angiographic Coronary Artery Disease and Paraoxonase Gene Polymorphisms in the National Heart, Lung, and Blood Institute.Sponsored Women.s Ischemia Syndrome Evaluation (WISE) Study, American journal of human genetics , 72(1), 2003, pp. 13-22
Authors:
Levinson, Douglas F.
Levinson, Matthew D.
Segurado, Ricardo
Lewis, Cathryn M.
Journal: American journal of human genetics
Citation: F. Levinson, Douglas et al., Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part I: Methods and Power Analysis, American journal of human genetics , 73(1), 2003, pp. 17-33
Authors:
Blom, Daniël
Speijer, Dave
Linthorst, Gabor E.
Donker-Koopman, Wilma G.
Strijland, Anneke
Aerts, M.F.G. Johannes
Journal: American journal of human genetics
Citation: Blom, Daniël et al., Recombinant Enzyme Therapy for Fabry Disease: Absence of Editing of Human .-Galactosidase A mRNA, American journal of human genetics , 72(1), 2003, pp. 23-31
Authors:
Gilbert, M. Thomas P.
Willerslev, Eske
Hansens, Anders J.
Barnes, Ian
Rudbeck, Lars
Lynnerup, Niels
Cooper, Alan
Journal: American journal of human genetics
Citation: P. Gilbert, M. Thomas et al., Distribution Patterns of Postmortem Damage in Human Mitochondrial DNA, American journal of human genetics , 72(1), 2003, pp. 32-47
Authors:
Lewis, Cathryn M.
Levinson, Douglas F.
Wise, Lesley H.
DeLisi, Lynn E.
Straub, Richard E.
Hovatta, Iiris
Williams, Nigel M.
Schwab, Sibylle G.
Pulver, Ann E.
Faraone, Stephen V.
Brzustowicz, Linda M.
Kaufmann, Charles A.
Garver, David L.
Gurling, Hugh M.D.
Lindholm, Eva
Coon, Hilary
Moises, Hans W.
Byerley, William
Shaw, Sarah H.
Mesen, Andrea
Sherrington, Robin
O'Neill, F. Anthony
Walsh, Dermot
Kendler, Kenneth S.
Ekelund, Jesper
Paunio, Tiina
Lönnqvist, Jouko
Peltonen, Leena
O'Donovan, Michael C.
Owen, Michael J.
Wildenauer, Dieter B.
Maier, Wolfgang
Nestadt, Gerald
Blouin, Jean-Louis
Antonarakis, Stylianos E.
Mowry, Bryan J.
Silverman, Jeremy M.
Crowe, Raymond R.
Cloninger, Robert C.
Tsuang, Jeremy M.
Malaspina, Dolores
Harkavy-Friedman, Jill M.
Svrakic, Dragan M.
Bassett, Anne S.
Holcomb, Jennifer
Kalsi, Gursharan
McQuillin, Andrew
Brynjolfson, Jon
Sigmundsson, Thordur
Petursson, Hannes
Jazin, Elena
Zoëga, Tomas
Helgason, Tomas
Journal: American journal of human genetics
Citation: M. Lewis, Cathryn et al., Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia, American journal of human genetics , 73(1), 2003, pp. 34-48
Authors:
Gilbert, M. Thomas P.
Hansen, Anders J.
Willerslev, Eske
Rudbeck, Lars
Barnes, Ian
Lynnerup, Niels
Cooper, Alan
Journal: American journal of human genetics
Citation: P. Gilbert, M. Thomas et al., Characterization of Genetic Miscoding Lesions Caused by Postmortem Damage, American journal of human genetics , 72(1), 2003, pp. 48-61
Authors:
Segurado, Ricardo
Detera-Wadleigh, Sevilla D.
Levinson, Douglas F.
Lewis, Cathryn M.
Gil, Michael
Nurnberger, John I., Jr.
Craddock, Nick
DePaulo, Raymond J.
Baron, Miron
Gershon, Elliot S.
Ekhoolm, Jenny
Cichon, Sven
Turecki, Gustavo
Claes, Stephan
Kelsoe, John R.
Badenhop, Renee F.
Morissette, J.
Coon, Hilary
Blackwood, Douglas
McInnes, L.Allison
Foroud, Tatiana
Edenberg, Howard J.
Reich, Theodore
Rice, John P.
Goate, Alison
McInnis, Melvin G.
McMahon, Francis J.
Badner, Judith A.
Goldin, Lynn R.
Bennett, Phil
Willour, Virginia L.
Zandi, Peter P.
Liu, Jianjun
Gillam, Conrad
Juo, Suh-Hang
Berrettini, Wade H.
Yoshikawa, Takeo
Peltonen, Leena
Lönnqvist, Juoko
Nöthen, Markus M.
Schumacher, Johannes
Windemuth, Christine
Rietschel, Marcella
Proppin, Peter
Maier, Wolfgang
Alda, Martin
Grof, Paul
Rouleau, Guy A.
Del-Favero, Jurgen
Van Broeckhoven, Christine
Mendlewicz, Julien
Adolfsson, Rolf
Spence, M. Anne
Luebbert, Hermann
Adams, Linda J.
Donald, Jennifer A.
Mitchell, Philip B.
Barden, Nicholas
Shink, Eric
Byerley, William
Muir, Walter
Visscher, Peter M.
Macgregor, Stuart
Gurling, Hugh
Kalsi, Gursharan
McQuillin, Andrew
Escamilla, Michael A.
Reus, Victor I.
Leon, Pedro
Freimer, Nelson B.
Ewald, Henrik
Kruse, Torben A.
Mors, Ole
Radhakrishna, Uppala
Blouin, Jean-Louis
Antonarakis, Stylianos
Akarsu, Nurten
Journal: American journal of human genetics
Citation: Segurado, Ricardo et al., Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder, American journal of human genetics , 73(1), 2003, pp. 49-62
Authors:
Yi, Zanhua
Garrison, Nanibaa
Cohen-Barak, Orit
Karafet, Tatiana M.
King, RIchard A.
Erickson, Robert P.
Hammer, Michael F.
Brilliant, Murray H.
Journal: American journal of human genetics
Citation: Yi, Zanhua et al., A 122.5-Kilobase Deletion of the P Gene Underlies the High Prevalence of Oculocutaneous Albinism Type 2 in the Navajo Population, American journal of human genetics , 72(1), 2003, pp. 62-72
Authors:
Zhang, Kui
Sun, Fengzhu
Wateran, Michael S.
Chen, Ting
Journal: American journal of human genetics
Citation: Zhang, Kui et al., Haplotype Block Partition with Limited Resources and Applications to Human Chromosome 21 Haplotype Data, American journal of human genetics , 73(1), 2003, pp. 63-73
Authors:
Abe, Satoko
Katagiri, Toyomasa
Saito-Hisaminato, Akihiko
Usami, Shin-ichi
Inoue, Yasuhiro
Tsunoda, Tatsuhiko
Nakamura, Yusuke
Journal: American journal of human genetics
Citation: Abe, Satoko et al., Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues, American journal of human genetics , 72(1), 2003, pp. 73-82
Authors:
Brassington, Anne-Marie E.
Sung, Sandy S.
Toydemir, Reha M.
Le, Trung
Roeder, Amy D.
Rutherford, Ann E.
Whitby, Frank G.
Jorde, Lynn B.
Bamshad, Michael J.
Journal: American journal of human genetics
Citation: E. Brassington, Anne-marie et al., Expressivity of Holt-Oram Syndrome Is Not Predicted by TBX5 Genotype, American journal of human genetics , 73(1), 2003, pp. 74-85
Authors:
Stefansson, Hreinn
Sarginson, Jane
Kong, Augustine
Yates, Phil
Steinthorsdottir, Valgerdur
Gudfinnson, Einar
Gunnarsdottir, Steinunn
Walker, Nicholas
Petursson, Hannes
Crombie, Caroline
Ingason, Andres
Gulcher, Jeffrey R.
Stefansson, Kari
St Clair, David
Journal: American journal of human genetics
Citation: Stefansson, Hreinn et al., Association of Neuregulin 1 with Schizophrenia Confirmed in a Scottish Population, American journal of human genetics , 72(1), 2003, pp. 83-87
Authors:
Manilla, H.
Koivisto, M.
Perola, M.
Varilo, T.
Hennah, W.
Ekelund, J.
Lukk, M.
Peltonen, L.
Ukkonen, E.
Journal: American journal of human genetics
Citation: H. Manilla, et al., Minimum Description Length Block Finder, a Method to Identify Haplotype Blocks and to Compare the Strength of Block Boundaries, American journal of human genetics , 73(1), 2003, pp. 86-94
Authors:
Borrego, Salud
Wright, Fred A.
Fernàndez, Raquel M.
Williams, Nita
Lòpez-Alonso, Manuel
Davuluri, Ramana
Antiñolo, Guillermo
Eng, Charis
Journal: American journal of human genetics
Citation: Borrego, Salud et al., A Founding Locus within the RET Proto-Oncogene May Account for a Large Proportion of Apparently Sporadic Hirschsprung Disease and a Subset of Cases of Sporadic Medullary Thyroid Carcinoma, American journal of human genetics , 72(1), 2003, pp. 88-100
Authors:
Toro, Jorge R.
Nickerson, Michael L.
Wei, Ming-Hui
Warren, Michelle B.
Glenn, Gladys M.
Turner, Maria L.
Stewart, Laveta
Durray, Paul
Tourre, Ousman
Sharma, Nirmala
Choyke, Peter
Stratton, Pamela
Merino, Maria
Walther, McClellan M.
Marston Linehan, W.
Schmidt, Laura S.
Zbar, Berton
Journal: American journal of human genetics
Citation: R. Toro, Jorge et al., Mutations in the Fumarate Hydratase Gene Cause Hereditary Leiomyomatosis and Renal Cell Cancer in Families in North America, American journal of human genetics , 73(1), 2003, pp. 95-106
Authors:
Antonicka, Hana
Mattman, Andre
Carlson, Christopher G.
Glerum, D. Moira
Hoffbuhr, Kristen C.
Leary, Scot C.
Kennaway, Nancy G.
Shoubridge, Eric A.
Journal: American journal of human genetics
Citation: Antonicka, Hana et al., Mutations in COX15 Produce a Defect in the Mitochondrial Heme Biosynthetic Pathway, Causing Early-Onset Fatal Hypertrophic Cardiomyopathy, American journal of human genetics , 72(1), 2003, pp. 101-114
Authors:
Dick, Danielle M.
Foroud, Tatiana
Flury, Leah
Bowman, Elizabeth S.
Miller, Marvin J.
Rau, N. Leela
Moe, P. Ryan
Samavedy, Nalini
El-Mallakh, Rif
Manji, Husseini
Glitz, Debra A.
Meyer, Eric T.
Smiley, Carrie
Hahn, Rhoda
Widmark, Clifford
McKinney, Rebecca
Sutton, Laura
Ballas, Christos
Grice, Dorothy
Berrettini, Wade
Byerley, William
Coryell, William
DePaulo, Raymond
MacKinnon, Dean F.
Gershon, Elliot S.
Kelsoe, John R.
McMahon, Francis J.
McInnis, Melvin
Murphy, Dennis L.
Reich, Theodore
Scheftner, William
Nurnberger, John I. , Jr.
Journal: American journal of human genetics
Citation: M. Dick, Danielle et al., Genomewide Linkage Analyses of Bipolar Disorder: A New Sample of 250 Pedigrees from the National Institute of Mental Health Genetics Initiative, American journal of human genetics , 73(1), 2003, pp. 107-114
Authors:
Dong, Chanhui
Wang, Shuang
Li, Wei-Dong
Li, Ding
Zhao, Hongyu
Price, R. Arlen
Journal: American journal of human genetics
Citation: Dong, Chanhui et al., Interacting Genetic Loci on Chromosomes 20 and 10 Influence Extreme Human Obesity, American journal of human genetics , 72(1), 2003, pp. 115-124
Authors:
Meng, Zhaoling
Zaykin, Dmitri V.
Xu, Chun-Fang
Wagner, Michael
Ehm, Margaret G.
Journal: American journal of human genetics
Citation: Meng, Zhaoling et al., Selection of Genetic Markers for Association Analyses, Using Linkage Disequilibrium and Haplotypes, American journal of human genetics , 73(1), 2003, pp. 115-130
Authors:
Karason, Ari
Gudjonsson, Johann E.
Upmanyu, Ruchi
Antonsdottir, Arna A.
Hauksson, Valdimar B.
Runasdottir, E. Hjaltey
Jonsson, Hjortur H.
Gudbjartsson, Daniel F.
Frigge, Micheal L.
Kong, Augustine
Stefansson, Kari
Valdimarsson, Helgi
Gulcher, Jeffrey R.
Journal: American journal of human genetics
Citation: Karason, Ari et al., A Susceptibility Gene for Psoriatic Arthritis Maps to Chromosome 16q: Evidence for Imprinting, American journal of human genetics , 72(1), 2003, pp. 125-131
Authors:
Bayés, Mònica
Magano, Luis F.
Rivera, Nùria
Flores, Raquel
Pérez Jurado, Luis A.
Journal: American journal of human genetics
Citation: Bayés, Mònica et al., Mutational Mechanisms of Williams-Beuren Syndrome Deletions, American journal of human genetics , 73(1), 2003, pp. 131-151
Authors:
Douglas, Jenny
Hanks, Sandra
Temple, I. Karen
Davies, Sally
Murray, Alexandra
Upadhyaya, Meena
Tomkins, Susan
Hughes, Helen E.
Cole, R.P. Trevor
Rahman, Nazneen
Journal: American journal of human genetics
Citation: Douglas, Jenny et al., NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes, American journal of human genetics , 72(1), 2003, pp. 132-143
Authors:
Wilson, S.G.
Reed, P.W.
Bansal, A.
Chiano, M.
Lindersson, M.
Langdown, M.
Prince, R.L.
Thompson, D.
Thompson, E.
Bailey, M.
Kleyn, P.W.
Sambrook, P.
Shi, M.M.
Spector, T.D.
Journal: American journal of human genetics
Citation: Wilson, S.g et al., Comparison of Genome Screens for Two Independent Cohorts Provides Replication of Suggestive Linkage of Bone Mineral Density to 3p21 and 1p36, American journal of human genetics , 72(1), 2003, pp. 144-155
Authors:
Bray, Nicholas J.
Buckland, Paul R.
Williams, Nigel M.
Norton, Nadine
Owen, Michael J.
O'Donovan, Michael C.
Williams, Hywel J.
Journal: American journal of human genetics
Citation: J. Bray, Nicholas et al., A Haplotype Implicated in Schizophrenia Susceptibility Is Associated with Reduced COMT Expression in Human Brain, American journal of human genetics , 73(1), 2003, pp. 152-161