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Aravinda Chakravarti

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Disorders

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Anatomy

Chromosomes, Human, Pair 21

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Physiology

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Publications

TOP 3
Weiss Lauren A; Arking Dan E; Daly Mark J; Chakravarti Aravinda
A genome-wide linkage and association scan reveals novel loci for autism.
Manolio Teri A; Collins Francis S; Cox Nancy J; Goldstein David B; Hindorff Lucia A; Hunter David J; McCarthy Mark I; Ramos Erin M; Cardon Lon R; Chakravarti Aravinda; Cho Judy H; Guttmacher Alan E; Kong Augustine; Kruglyak Leonid; Mardis Elaine; Rotimi Charles N; Slatkin Montgomery; Valle David; Whittemore Alice S; Boehnke Michael; Clark Andrew G; Eichler Evan E; Gibson Greg; Haines Jonathan L; Mackay Trudy F C; McCarroll Steven A; Visscher Peter M
Finding the missing heritability of complex diseases.
Chakravarti Aravinda
Human genetics: Tracing India's invisible threads.

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All Publications

2009: Weiss Lauren A; Arking Dan E; Daly Mark J; Chakravarti Aravinda
A genome-wide linkage and association scan reveals novel loci for autism.
Nature 2009;461(7265):802-8.
2009: Manolio Teri A; Collins Francis S; Cox Nancy J; Goldstein David B; Hindorff Lucia A; Hunter David J; McCarthy Mark I; Ramos Erin M; Cardon Lon R; Chakravarti Aravinda; Cho Judy H; Guttmacher Alan E; Kong Augustine; Kruglyak Leonid; Mardis Elaine; Rotimi Charles N; Slatkin Montgomery; Valle David; Whittemore Alice S; Boehnke Michael; Clark Andrew G; Eichler Evan E; Gibson Greg; Haines Jonathan L; Mackay Trudy F C; McCarroll Steven A; Visscher Peter M
Finding the missing heritability of complex diseases.
Nature 2009;461(7265):747-53.
2009: Chakravarti Aravinda
Human genetics: Tracing India's invisible threads.
Nature 2009;461(7263):487-8.
2009: Arking Dan E; Chakravarti Aravinda
Understanding cardiovascular disease through the lens of genome-wide association studies.
Trends in genetics : TIG 2009;25(9):387-94.
2009: Milan David J; Kim Albert M; Winterfield Jeffrey R; Jones Ian L; Pfeufer Arne; Sanna Serena; Arking Dan E; Amsterdam Adam H; Sabeh Khaled M; Mably John D; Rosenbaum David S; Peterson Randall T; Chakravarti Aravinda; Kääb Stefan; Roden Dan M; MacRae Calum A
Drug-sensitized zebrafish screen identifies multiple genes, including GINS3, as regulators of myocardial repolarization.
Circulation 2009;120(7):553-9.
2009: Joe Bina; Saad Yasser; Lee Norman H; Frank Bryan C; Achinike Ovokeraye H; Luu Truong V; Gopalakrishnan Kathirvel; Toland Edward J; Farms Phyllis; Yerga-Woolwine Shane; Manickavasagam Ezhilarasi; Rapp John P; Garrett Michael R; Coe David; Apte Suneel S; Rankinen Tuomo; Pérusse Louis; Ehret Georg B; Ganesh Santhi K; Cooper Richard S; O'Connor Ashley; Rice Treva; Weder Alan B; Chakravarti Aravinda; Rao Dabeeru C; Bouchard Claude
Positional identification of variants of Adamts16 linked to inherited hypertension.
Human molecular genetics 2009;18(15):2825-38.
2009: Arnold Stacey; Pelet Anna; Amiel Jeanne; Borrego Salud; Hofstra Robert; Tam Paul; Ceccherini Isabella; Lyonnet Stanislas; Sherman Stephanie; Chakravarti Aravinda
Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association.
Human mutation 2009;30(5):771-5.
2009: Franceschini Nora; North Kari E; Arnett Donna; Pankow James S; Chung Jay H; Baird Lisa; Leppert Mark F; Eckfeldt John H; Boerwinkle Eric; Gu C Charles; Lewis Cora E; Myers Richard H; Turner Stephen T; Weder Alan; Kao W H Linda; Mosley Thomas H; Chakravarti Aravinda; Kramer Holly; Zhang Jinghui; Hunt Steven C
The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study.
American journal of hypertension 2009;22(5):552-8.
2009: Pfeufer Arne; Sanna Serena; Arking Dan E; Müller Martina; Gateva Vesela; Fuchsberger Christian; Ehret Georg B; Orrú Marco; Pattaro Cristian; Köttgen Anna; Perz Siegfried; Usala Gianluca; Barbalic Maja; Li Man; Pütz Benno; Scuteri Angelo; Prineas Ronald J; Sinner Moritz F; Gieger Christian; Najjar Samer S; Kao W H Linda; Mühleisen Thomas W; Dei Mariano; Happle Christine; Möhlenkamp Stefan; Crisponi Laura; Erbel Raimund; Jöckel Karl-Heinz; Naitza Silvia; Steinbeck Gerhard; Marroni Fabio; Hicks Andrew A; Lakatta Edward; Müller-Myhsok Bertram; Pramstaller Peter P; Wichmann H-Erich; Schlessinger David; Boerwinkle Eric; Meitinger Thomas; Uda Manuela; Coresh Josef; Kääb Stefan; Abecasis Gonçalo R; Chakravarti Aravinda
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
Nature genetics 2009;41(4):407-14.
2009: Dezentje David A; Arking Dan E; Kortenhorst Madeleine S Q; West Kristen; Chakravarti Aravinda; Kern Scott E
Hybrids of aneuploid human cancer cells permit complementation of simple and complex cancer defects.
Cancer biology & therapy 2009;8(4):347-55.
2009: Kao W H Linda; Arking Dan E; Post Wendy; Rea Thomas D; Sotoodehnia Nona; Prineas Ronald J; Bishe Bryan; Doan Betty Q; Boerwinkle Eric; Psaty Bruce M; Tomaselli Gordon F; Coresh Josef; Siscovick David S; Marbán Eduardo; Spooner Peter M; Burke Gregory L; Chakravarti Aravinda
Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.
Circulation 2009;119(7):940-51.
2009: Chakravarti Aravinda
Being human: kinship: race relations.
Nature 2009;457(7228):380-1.
2009: Wang Ying; O'Connell Jeffrey R; McArdle Patrick F; Wade James B; Dorff Sarah E; Shah Sanjiv J; Shi Xiaolian; Pan Lin; Rampersaud Evadnie; Shen Haiqing; Kim James D; Subramanya Arohan R; Steinle Nanette I; Parsa Afshin; Ober Carole C; Welling Paul A; Chakravarti Aravinda; Weder Alan B; Cooper Richard S; Mitchell Braxton D; Shuldiner Alan R; Chang Yen-Pei C
From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(1):226-31.
2009: SanGiovanni John Paul; Arking Dan E; Iyengar Sudha K; Elashoff Michael; Clemons Traci E; Reed George F; Henning Alice K; Sivakumaran Theru A; Xu Xuming; DeWan Andrew; Agrón Elvira; Rochtchina Elena; Sue Carolyn M; Wang Jie Jin; Mitchell Paul; Hoh Josephine; Francis Peter J; Klein Michael L; Chew Emily Y; Chakravarti Aravinda
Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration.
PloS one 2009;4(5):e5508.
2009: Arking Dan E; Khera Amit; Xing Chao; Kao W H Linda; Post Wendy; Boerwinkle Eric; Chakravarti Aravinda
Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population.
PloS one 2009;4(1):e4333.
2008: Ehret Georg B; Morrison Alanna C; O'Connor Ashley A; Grove Megan L; Baird Lisa; Schwander Karen; Weder Alan; Cooper Richard S; Rao D C; Hunt Steven C; Boerwinkle Eric; Chakravarti Aravinda
Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program.
European journal of human genetics : EJHG 2008;16(12):1507-11.
2008: Chakravarti Aravinda
Obituary: Victor Almon McKusick (1921-2008).
Nature 2008;455(7209):46.
2008: Wang Wenyi; Carvalho Benilton; Miller Nathaniel D; Pevsner Jonathan; Chakravarti Aravinda; Irizarry Rafael A
Estimating genome-wide copy number using allele-specific mixture models.
Journal of computational biology : a journal of computational molecular cell biology 2008;15(7):857-66.
2008: Hastie Nick; Chakravarti Aravinda
Genetics of disease.
Current opinion in genetics & development 2008;18(3):227-8.
2008: Weiss Lauren A; Shen Yiping; Korn Joshua M; Arking Dan E; Miller David T; Fossdal Ragnheidur; Saemundsen Evald; Stefansson Hreinn; Ferreira Manuel A R; Green Todd; Platt Orah S; Ruderfer Douglas M; Walsh Christopher A; Altshuler David; Chakravarti Aravinda; Tanzi Rudolph E; Stefansson Kari; Santangelo Susan L; Gusella James F; Sklar Pamela; Wu Bai-Lin; Daly Mark J;
Association between microdeletion and microduplication at 16p11.2 and autism.
The New England journal of medicine 2008;358(7):667-75.
2008: Arking Dan E; Cutler David J; Brune Camille W; Teslovich Tanya M; West Kristen; Ikeda Morna; Rea Alexis; Guy Moltu; Lin Shin; Cook Edwin H; Chakravarti Aravinda
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
American journal of human genetics 2008;82(1):160-4.
2008: Tan Aik Choon; Fan Jian-Bing; Karikari Collins; Bibikova Marina; Garcia Eliza Wickham; Zhou Lixin; Barker David; Serre David; Feldmann Georg; Hruban Ralph H; Klein Alison P; Goggins Michael; Couch Fergus J; Hudson Thomas J; Winslow Raimond L; Maitra Anirban; Chakravarti Aravinda
Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discovery.
Cancer biology & therapy 2008;7(1):135-44.
2008: Amiel J; Sproat-Emison E; Garcia-Barcelo M; Lantieri F; Burzynski G; Borrego S; Pelet A; Arnold S; Miao X; Griseri P; Brooks A S; Antinolo G; de Pontual L; Clement-Ziza M; Munnich A; Kashuk C; West K; Wong K K-Y; Lyonnet S; Chakravarti A; Tam P K-H; Ceccherini I; Hofstra R M W; Fernandez R;
Hirschsprung disease, associated syndromes and genetics: a review.
Journal of medical genetics 2008;45(1):1-14.
2007: Sabeti Pardis C; Varilly Patrick; Fry Ben; Lohmueller Jason; Hostetter Elizabeth; Cotsapas Chris; Xie Xiaohui; Byrne Elizabeth H; McCarroll Steven A; Gaudet Rachelle; Schaffner Stephen F; Lander Eric S; Frazer Kelly A; Ballinger Dennis G; Cox David R; Hinds David A; Stuve Laura L; Gibbs Richard A; Belmont John W; Boudreau Andrew; Hardenbol Paul; Leal Suzanne M; Pasternak Shiran; Wheeler David A; Willis Thomas D; Yu Fuli; Yang Huanming; Zeng Changqing; Gao Yang; Hu Haoran; Hu Weitao; Li Chaohua; Lin Wei; Liu Siqi; Pan Hao; Tang Xiaoli; Wang Jian; Wang Wei; Yu Jun; Zhang Bo; Zhang Qingrun; Zhao Hongbin; Zhao Hui; Zhou Jun; Gabriel Stacey B; Barry Rachel; Blumenstiel Brendan; Camargo Amy; Defelice Matthew; Faggart Maura; Goyette Mary; Gupta Supriya; Moore Jamie; Nguyen Huy; Onofrio Robert C; Parkin Melissa; Roy Jessica; Stahl Erich; Winchester Ellen; Ziaugra Liuda; Altshuler David; Shen Yan; Yao Zhijian; Huang Wei; Chu Xun; He Yungang; Jin Li; Liu Yangfan; Shen Yayun; Sun Weiwei; Wang Haifeng; Wang Yi; Wang Ying; Xiong Xiaoyan; Xu Liang; Waye Mary M Y; Tsui Stephen K W; Xue Hong; Wong J Tze-Fei; Galver Luana M; Fan Jian-Bing; Gunderson Kevin; Murray Sarah S; Oliphant Arnold R; Chee Mark S; Montpetit Alexandre; Chagnon Fanny; Ferretti Vincent; Leboeuf Martin; Olivier Jean-François; Phillips Michael S; Roumy Stéphanie; Sallée Clémentine; Verner Andrei; Hudson Thomas J; Kwok Pui-Yan; Cai Dongmei; Koboldt Daniel C; Miller Raymond D; Pawlikowska Ludmila; Taillon-Miller Patricia; Xiao Ming; Tsui Lap-Chee; Mak William; Song You Qiang; Tam Paul K H; Nakamura Yusuke; Kawaguchi Takahisa; Kitamoto Takuya; Morizono Takashi; Nagashima Atsushi; Ohnishi Yozo; Sekine Akihiro; Tanaka Toshihiro; Tsunoda Tatsuhiko; Deloukas Panos; Bird Christine P; Delgado Marcos; Dermitzakis Emmanouil T; Gwilliam Rhian; Hunt Sarah; Morrison Jonathan; Powell Don; Stranger Barbara E; Whittaker Pamela; Bentley David R; Daly Mark J; de Bakker Paul I W; Barrett Jeff; Chretien Yves R; Maller Julian; McCarroll Steve; Patterson Nick; Pe'er Itsik; Price Alkes; Purcell Shaun; Richter Daniel J; Sabeti Pardis; Saxena Richa; Schaffner Stephen F; Sham Pak C; Varilly Patrick; Altshuler David; Stein Lincoln D; Krishnan Lalitha; Smith Albert Vernon; Tello-Ruiz Marcela K; Thorisson Gudmundur A; Chakravarti Aravinda; Chen Peter E; Cutler David J; Kashuk Carl S; Lin Shin; Abecasis Gonçalo R; Guan Weihua; Li Yun; Munro Heather M; Qin Zhaohui Steve; Thomas Daryl J; McVean Gilean; Auton Adam; Bottolo Leonardo; Cardin Niall; Eyheramendy Susana; Freeman Colin; Marchini Jonathan; Myers Simon; Spencer Chris; Stephens Matthew; Donnelly Peter; Cardon Lon R; Clarke Geraldine; Evans David M; Morris Andrew P; Weir Bruce S; Tsunoda Tatsuhiko; Johnson Todd A; Mullikin James C; Sherry Stephen T; Feolo Michael; Skol Andrew; Zhang Houcan; Zeng Changqing; Zhao Hui; Matsuda Ichiro; Fukushima Yoshimitsu; Macer Darryl R; Suda Eiko; Rotimi Charles N; Adebamowo Clement A; Ajayi Ike; Aniagwu Toyin; Marshall Patricia A; Nkwodimmah Chibuzor; Royal Charmaine D M; Leppert Mark F; Dixon Missy; Peiffer Andy; Qiu Renzong; Kent Alastair; Kato Kazuto; Niikawa Norio; Adewole Isaac F; Knoppers Bartha M; Foster Morris W; Clayton Ellen Wright; Watkin Jessica; Gibbs Richard A; Belmont John W; Muzny Donna; Nazareth Lynne; Sodergren Erica; Weinstock George M; Wheeler David A; Yakub Imtaz; Gabriel Stacey B; Onofrio Robert C; Richter Daniel J; Ziaugra Liuda; Birren Bruce W; Daly Mark J; Altshuler David; Wilson Richard K; Fulton Lucinda L; Rogers Jane; Burton John; Carter Nigel P; Clee Christopher M; Griffiths Mark; Jones Matthew C; McLay Kirsten; Plumb Robert W; Ross Mark T; Sims Sarah K; Willey David L; Chen Zhu; Han Hua; Kang Le; Godbout Martin; Wallenburg John C; L'Archevêque Paul; Bellemare Guy; Saeki Koji; Wang Hongguang; An Daochang; Fu Hongbo; Li Qing; Wang Zhen; Wang Renwu; Holden Arthur L; Brooks Lisa D; McEwen Jean E; Guyer Mark S; Wang Vivian Ota; Peterson Jane L; Shi Michael; Spiegel Jack; Sung Lawrence M; Zacharia Lynn F; Collins Francis S; Kennedy Karen; Jamieson Ruth; Stewart John
Genome-wide detection and characterization of positive selection in human populations.
Nature 2007;449(7164):913-8.
2007: Frazer Kelly A; Ballinger Dennis G; Cox David R; Hinds David A; Stuve Laura L; Gibbs Richard A; Belmont John W; Boudreau Andrew; Hardenbol Paul; Leal Suzanne M; Pasternak Shiran; Wheeler David A; Willis Thomas D; Yu Fuli; Yang Huanming; Zeng Changqing; Gao Yang; Hu Haoran; Hu Weitao; Li Chaohua; Lin Wei; Liu Siqi; Pan Hao; Tang Xiaoli; Wang Jian; Wang Wei; Yu Jun; Zhang Bo; Zhang Qingrun; Zhao Hongbin; Zhao Hui; Zhou Jun; Gabriel Stacey B; Barry Rachel; Blumenstiel Brendan; Camargo Amy; Defelice Matthew; Faggart Maura; Goyette Mary; Gupta Supriya; Moore Jamie; Nguyen Huy; Onofrio Robert C; Parkin Melissa; Roy Jessica; Stahl Erich; Winchester Ellen; Ziaugra Liuda; Altshuler David; Shen Yan; Yao Zhijian; Huang Wei; Chu Xun; He Yungang; Jin Li; Liu Yangfan; Shen Yayun; Sun Weiwei; Wang Haifeng; Wang Yi; Wang Ying; Xiong Xiaoyan; Xu Liang; Waye Mary M Y; Tsui Stephen K W; Xue Hong; Wong J Tze-Fei; Galver Luana M; Fan Jian-Bing; Gunderson Kevin; Murray Sarah S; Oliphant Arnold R; Chee Mark S; Montpetit Alexandre; Chagnon Fanny; Ferretti Vincent; Leboeuf Martin; Olivier Jean-François; Phillips Michael S; Roumy Stéphanie; Sallée Clémentine; Verner Andrei; Hudson Thomas J; Kwok Pui-Yan; Cai Dongmei; Koboldt Daniel C; Miller Raymond D; Pawlikowska Ludmila; Taillon-Miller Patricia; Xiao Ming; Tsui Lap-Chee; Mak William; Song You Qiang; Tam Paul K H; Nakamura Yusuke; Kawaguchi Takahisa; Kitamoto Takuya; Morizono Takashi; Nagashima Atsushi; Ohnishi Yozo; Sekine Akihiro; Tanaka Toshihiro; Tsunoda Tatsuhiko; Deloukas Panos; Bird Christine P; Delgado Marcos; Dermitzakis Emmanouil T; Gwilliam Rhian; Hunt Sarah; Morrison Jonathan; Powell Don; Stranger Barbara E; Whittaker Pamela; Bentley David R; Daly Mark J; de Bakker Paul I W; Barrett Jeff; Chretien Yves R; Maller Julian; McCarroll Steve; Patterson Nick; Pe'er Itsik; Price Alkes; Purcell Shaun; Richter Daniel J; Sabeti Pardis; Saxena Richa; Schaffner Stephen F; Sham Pak C; Varilly Patrick; Altshuler David; Stein Lincoln D; Krishnan Lalitha; Smith Albert Vernon; Tello-Ruiz Marcela K; Thorisson Gudmundur A; Chakravarti Aravinda; Chen Peter E; Cutler David J; Kashuk Carl S; Lin Shin; Abecasis Gonçalo R; Guan Weihua; Li Yun; Munro Heather M; Qin Zhaohui Steve; Thomas Daryl J; McVean Gilean; Auton Adam; Bottolo Leonardo; Cardin Niall; Eyheramendy Susana; Freeman Colin; Marchini Jonathan; Myers Simon; Spencer Chris; Stephens Matthew; Donnelly Peter; Cardon Lon R; Clarke Geraldine; Evans David M; Morris Andrew P; Weir Bruce S; Tsunoda Tatsuhiko; Mullikin James C; Sherry Stephen T; Feolo Michael; Skol Andrew; Zhang Houcan; Zeng Changqing; Zhao Hui; Matsuda Ichiro; Fukushima Yoshimitsu; Macer Darryl R; Suda Eiko; Rotimi Charles N; Adebamowo Clement A; Ajayi Ike; Aniagwu Toyin; Marshall Patricia A; Nkwodimmah Chibuzor; Royal Charmaine D M; Leppert Mark F; Dixon Missy; Peiffer Andy; Qiu Renzong; Kent Alastair; Kato Kazuto; Niikawa Norio; Adewole Isaac F; Knoppers Bartha M; Foster Morris W; Clayton Ellen Wright; Watkin Jessica; Gibbs Richard A; Belmont John W; Muzny Donna; Nazareth Lynne; Sodergren Erica; Weinstock George M; Wheeler David A; Yakub Imtaz; Gabriel Stacey B; Onofrio Robert C; Richter Daniel J; Ziaugra Liuda; Birren Bruce W; Daly Mark J; Altshuler David; Wilson Richard K; Fulton Lucinda L; Rogers Jane; Burton John; Carter Nigel P; Clee Christopher M; Griffiths Mark; Jones Matthew C; McLay Kirsten; Plumb Robert W; Ross Mark T; Sims Sarah K; Willey David L; Chen Zhu; Han Hua; Kang Le; Godbout Martin; Wallenburg John C; L'Archevêque Paul; Bellemare Guy; Saeki Koji; Wang Hongguang; An Daochang; Fu Hongbo; Li Qing; Wang Zhen; Wang Renwu; Holden Arthur L; Brooks Lisa D; McEwen Jean E; Guyer Mark S; Wang Vivian Ota; Peterson Jane L; Shi Michael; Spiegel Jack; Sung Lawrence M; Zacharia Lynn F; Collins Francis S; Kennedy Karen; Jamieson Ruth; Stewart John
A second generation human haplotype map of over 3.1 million SNPs.
Nature 2007;449(7164):851-61.
2007: Gherman Adrian; Chen Peter E; Teslovich Tanya M; Stankiewicz Pawel; Withers Marjorie; Kashuk Carl S; Chakravarti Aravinda; Lupski James R; Cutler David J; Katsanis Nicholas
Population bottlenecks as a potential major shaping force of human genome architecture.
PLoS genetics 2007;3(7):e119.
2007: Scuteri Angelo; Sanna Serena; Chen Wei-Min; Uda Manuela; Albai Giuseppe; Strait James; Najjar Samer; Nagaraja Ramaiah; Orrú Marco; Usala Gianluca; Dei Mariano; Lai Sandra; Maschio Andrea; Busonero Fabio; Mulas Antonella; Ehret Georg B; Fink Ashley A; Weder Alan B; Cooper Richard S; Galan Pilar; Chakravarti Aravinda; Schlessinger David; Cao Antonio; Lakatta Edward; Abecasis Gonçalo R
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.
PLoS genetics 2007;3(7):e115.
2007: Wen Gen; Wessel Jennifer; Zhou Weidong; Ehret Georg B; Rao Fangwen; Stridsberg Mats; Mahata Sushil K; Gent Peter M; Das Madhusudan; Cooper Richard S; Chakravarti Aravinda; Zhou Huilin; Schork Nicholas J; O'connor Daniel T; Hamilton Bruce A
An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension.
Human molecular genetics 2007;16(14):1752-64.
2007: Gu C Charles; Hunt Steven C; Kardia Sharon; Turner Stephen T; Chakravarti Aravinda; Schork Nicholas; Olshen Richard; Curb David; Jaquish Cashell; Boerwinkle Eric; Rao D C
An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP).
Human genetics 2007;121(5):577-90.
2007: Zlotogora J; Hujerat Y; Barges S; Shalev S A; Chakravarti A
The fate of 12 recessive mutations in a single village.
Annals of human genetics 2007;71(Pt 2):202-8.
2007: Chang Yen-Pei Christy; Liu Xin; Kim James Dae Ok; Ikeda Morna A; Layton Marnie R; Weder Alan B; Cooper Richard S; Kardia Sharon L R; Rao D C; Hunt Steve C; Luke Amy; Boerwinkle Eric; Chakravarti Aravinda
Multiple genes for essential-hypertension susceptibility on chromosome 1q.
American journal of human genetics 2007;80(2):253-64.
2007: Post Wendy; Shen Haiqing; Damcott Coleen; Arking Dan E; Kao W H Linda; Sack Paul A; Ryan Kathleen A; Chakravarti Aravinda; Mitchell Braxton D; Shuldiner Alan R
Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish.
Human heredity 2007;64(4):214-9.
2006: Blackman Scott M; Deering-Brose Rebecca; McWilliams Rita; Naughton Kathleen; Coleman Barbara; Lai Teresa; Algire Marilyn; Beck Suzanne; Hoover-Fong Julie; Hamosh Ada; Fallin M Daniele; West Kristen; Arking Dan E; Chakravarti Aravinda; Cutler David J; Cutting Garry R
Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis.
Gastroenterology 2006;131(4):1030-9.
2006: Bibikova Marina; Chudin Eugene; Wu Bonnie; Zhou Lixin; Garcia Eliza Wickham; Liu Ying; Shin Soojung; Plaia Todd W; Auerbach Jonathan M; Arking Dan E; Gonzalez Rodolfo; Crook Jeremy; Davidson Bruce; Schulz Thomas C; Robins Allan; Khanna Aparna; Sartipy Peter; Hyllner Johan; Vanguri Padmavathy; Savant-Bhonsale Smita; Smith Alan K; Chakravarti Aravinda; Maitra Anirban; Rao Mahendra; Barker David L; Loring Jeanne F; Fan Jian-Bing
Human embryonic stem cells have a unique epigenetic signature.
Genome research 2006;16(9):1075-83.
2006: Calhoun Eric S; Hucl Tomas; Gallmeier Eike; West Kristen M; Arking Dan E; Maitra Anirban; Iacobuzio-Donahue Christine A; Chakravarti Aravinda; Hruban Ralph H; Kern Scott E
Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.
Cancer research 2006;66(16):7920-8.
2006: Arking Dan E; Pfeufer Arne; Post Wendy; Kao W H Linda; Newton-Cheh Christopher; Ikeda Morna; West Kristen; Kashuk Carl; Akyol Mahmut; Perz Siegfried; Jalilzadeh Shapour; Illig Thomas; Gieger Christian; Guo Chao-Yu; Larson Martin G; Wichmann H Erich; Marbán Eduardo; O'Donnell Christopher J; Hirschhorn Joel N; Kääb Stefan; Spooner Peter M; Meitinger Thomas; Chakravarti Aravinda
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
Nature genetics 2006;38(6):644-51.
2006: Arking Dan E; Fallin Daniele M; Fried Linda P; Li Tao; Beamer Brock A; Xue Qian Li; Chakravarti Aravinda; Walston Jeremy
Variation in the ciliary neurotrophic factor gene and muscle strength in older Caucasian women.
Journal of the American Geriatrics Society 2006;54(5):823-6.
2006: Chang Yen-Pei Christy; Kim James Dae-Ok; Schwander Karen; Rao Dabeeru C; Miller Mike B; Weder Alan B; Cooper Richard S; Schork Nicholas J; Province Michael A; Morrison Alanna C; Kardia Sharon L R; Quertermous Thomas; Chakravarti Aravinda
The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.
European journal of human genetics : EJHG 2006;14(4):469-77.
2006: Zlotogora Joël; Carasquillo Minerva; Barges Saleh; Shalev Stavit A; Hujerat Yasir; Chakravarti Aravinda
High incidence of deafness from three frequent connexin 26 mutations in an isolated community.
Genetic testing 2006;10(1):40-3.
2006: Laramie Jason M; Wilk Jemma B; Hunt Steven C; Ellison R Curtis; Chakravarti Aravinda; Boerwinkle Eric; Myers Richard H
Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program.
BMC medical genetics 2006;7():17.
2005: Young J Hunter; Chang Yen-Pei C; Kim James Dae-Ok; Chretien Jean-Paul; Klag Michael J; Levine Michael A; Ruff Christopher B; Wang Nae-Yuh; Chakravarti Aravinda
Differential susceptibility to hypertension is due to selection during the out-of-Africa expansion.
PLoS genetics 2005;1(6):e82.
2005: Rasmussen-Torvik Laura J; North Kari E; Gu C Charles; Lewis Cora E; Wilk Jemma B; Chakravarti Aravinda; Chang Yen-Pei C; Miller Michael B; Li Na; Devereux Richard B; Arnett Donna K
A population association study of angiotensinogen polymorphisms and haplotypes with left ventricular phenotypes.
Hypertension 2005;46(6):1294-9.
2005: Grice Elizabeth A; Rochelle Erin S; Green Eric D; Chakravarti Aravinda; McCallion Andrew S
Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer.
Human molecular genetics 2005;14(24):3837-45.
2005: Armanios Mary; Chen Jiunn-Liang; Chang Yen-Pei Christy; Brodsky Robert A; Hawkins Anita; Griffin Constance A; Eshleman James R; Cohen Alan R; Chakravarti Aravinda; Hamosh Ada; Greider Carol W
Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(44):15960-4.
2005: Maitra Anirban; Arking Dan E; Shivapurkar Narayan; Ikeda Morna; Stastny Victor; Kassauei Keyaunoosh; Sui Guoping; Cutler David J; Liu Ying; Brimble Sandii N; Noaksson Karin; Hyllner Johan; Schulz Thomas C; Zeng Xianmin; Freed William J; Crook Jeremy; Abraham Suman; Colman Alan; Sartipy Peter; Matsui Sei-Ichi; Carpenter Melissa; Gazdar Adi F; Rao Mahendra; Chakravarti Aravinda
Genomic alterations in cultured human embryonic stem cells.
Nature genetics 2005;37(10):1099-103.
2005: Zlotogora Joël; Hujerat Yasir; Zalman Luci; Barges Saleh; Filon Dori; Koren Ariel; Shalev Stavit A; Chakravarti Aravinda
Origin and expansion of four different beta globin mutations in a single Arab village.
American journal of human biology : the official journal of the Human Biology Council 2005;17(5):659-61.
2005: Mitchell Adele A; Chakravarti Aravinda; Cutler David J
On the probability that a novel variant is a disease-causing mutation.
Genome research 2005;15(7):960-6.
2005: Kashuk Carl S; Stone Eric A; Grice Elizabeth A; Portnoy Matthew E; Green Eric D; Sidow Arend; Chakravarti Aravinda; McCallion Andrew S
Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(25):8949-54.
2005: Mulle J G; Chowdari K V; Nimgaonkar V; Chakravarti A
No evidence for association to the G72/G30 locus in an independent sample of schizophrenia families.
Molecular psychiatry 2005;10(5):431-3.
2005: Mulle J G; McDonough J A; Chowdari K V; Nimgaonkar V; Chakravarti A
Evidence for linkage to chromosome 13q32 in an independent sample of schizophrenia families.
Molecular psychiatry 2005;10(5):429-31.
2005: Emison Eileen Sproat; McCallion Andrew S; Kashuk Carl S; Bush Richard T; Grice Elizabeth; Lin Shin; Portnoy Matthew E; Cutler David J; Green Eric D; Chakravarti Aravinda
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.
Nature 2005;434(7035):857-63.
2005: Walston J; Arking D E; Fallin D; Li T; Beamer B; Xue Q; Ferrucci L; Fried L P; Chakravarti A
IL-6 gene variation is not associated with increased serum levels of IL-6, muscle, weakness, or frailty in older women.
Experimental gerontology 2005;40(4):344-52.
2005: Gu C Charles; Chang Yen-Pei C; Hunt Steven C; Schwander Karen; Arnett Donna; Djousse Luc; Heiss Gerardo; Oberman Al; Lalouel Jean-Marc; Province Mike; Chakravarti Aravinda; Rao D C
Haplotype association analysis of AGT variants with hypertension-related traits: the HyperGEN study.
Human heredity 2005;60(3):164-76.
2004: Lin Shin; Chakravarti Aravinda; Cutler David J
Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.
Nature genetics 2004;36(11):1181-8.
2004: Chakravarti Aravinda
Finding needles in haystacks--IRF6 gene variants in isolated cleft lip or cleft palate.
The New England journal of medicine 2004;351(8):822-4.
2004: Lin Shin; Chakravarti Aravinda; Cutler David J
Haplotype and missing data inference in nuclear families.
Genome research 2004;14(8):1624-32.
2004: Maitra Anirban; Cohen Yoram; Gillespie Susannah E D; Mambo Elizabeth; Fukushima Noriyoshi; Hoque Mohammad O; Shah Nila; Goggins Michael; Califano Joseph; Sidransky David; Chakravarti Aravinda
The Human MitoChip: a high-throughput sequencing microarray for mitochondrial mutation detection.
Genome research 2004;14(5):812-9.
2004: Mitchell Adele A; Zwick Michael E; Chakravarti Aravinda; Cutler David J
Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns.
Bioinformatics (Oxford, England) 2004;20(7):1022-32.
2004: Arking Dan E; Chugh Sumeet S; Chakravarti Aravinda; Spooner Peter M
Genomics in sudden cardiac death.
Circulation research 2004;94(6):712-23.
2004: Hong Hee-Kyung; Chakravarti Aravinda; Takahashi Joseph S
The gene for soluble N-ethylmaleimide sensitive factor attachment protein alpha is mutated in hydrocephaly with hop gait (hyh) mice.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(6):1748-53.
2004: Xu Zhiying; Kerstann Kimberly F; Sherman Stephanie L; Chakravarti Aravinda; Feingold Eleanor
A trisomic transmission disequilibrium test.
Genetic epidemiology 2004;26(2):125-31.
2004: Barkley Ruth Ann; Chakravarti Aravinda; Cooper Richard S; Ellison R Curtis; Hunt Steven C; Province Michael A; Turner Stephen T; Weder Alan B; Boerwinkle Eric;
Positional identification of hypertension susceptibility genes on chromosome 2.
Hypertension 2004;43(2):477-82.
2003: Faden Ruth R; Dawson Liza; Bateman-House Alison S; Agnew Dawn Mueller; Bok Hilary; Brock Dan W; Chakravarti Aravinda; Gao Xiao-Jiang; Greene Mark; Hansen John A; King Patricia A; O'Brien Stephen J; Sachs David H; Schill Kathryn E; Siegel Andrew; Solter Davor; Suter Sonia M; Verfaillie Catherine M; Walters LeRoy B; Gearhart John D
Public stem cell banks: considerations of justice in stem cell research and therapy.
The Hastings Center report 2003;33(6):13-27.
2003: Dawson Liza; Bateman-House Alison S; Mueller Agnew Dawn; Bok Hilary; Brock Dan W; Chakravarti Aravinda; Greene Mark; King Patricia A; O'Brien Stephen J; Sachs David H; Schill Kathryn E; Siegel Andrew; Solter Davor; Suter Sonia M; Verfaillie Catherine M; Walters LeRoy B; Gearhart John D; Faden Ruth R
Safety issues in cell-based intervention trials.
Fertility and sterility 2003;80(5):1077-85.
2003: Peri Suraj; Navarro J Daniel; Amanchy Ramars; Kristiansen Troels Z; Jonnalagadda Chandra Kiran; Surendranath Vineeth; Niranjan Vidya; Muthusamy Babylakshmi; Gandhi T K B; Gronborg Mads; Ibarrola Nieves; Deshpande Nandan; Shanker K; Shivashankar H N; Rashmi B P; Ramya M A; Zhao Zhixing; Chandrika K N; Padma N; Harsha H C; Yatish A J; Kavitha M P; Menezes Minal; Choudhury Dipanwita Roy; Suresh Shubha; Ghosh Neelanjana; Saravana R; Chandran Sreenath; Krishna Subhalakshmi; Joy Mary; Anand Sanjeev K; Madavan V; Joseph Ansamma; Wong Guang W; Schiemann William P; Constantinescu Stefan N; Huang Lily; Khosravi-Far Roya; Steen Hanno; Tewari Muneesh; Ghaffari Saghi; Blobe Gerard C; Dang Chi V; Garcia Joe G N; Pevsner Jonathan; Jensen Ole N; Roepstorff Peter; Deshpande Krishna S; Chinnaiyan Arul M; Hamosh Ada; Chakravarti Aravinda; Pandey Akhilesh
Development of human protein reference database as an initial platform for approaching systems biology in humans.
Genome research 2003;13(10):2363-71.
2003: Thomas J W; Touchman J W; Blakesley R W; Bouffard G G; Beckstrom-Sternberg S M; Margulies E H; Blanchette M; Siepel A C; Thomas P J; McDowell J C; Maskeri B; Hansen N F; Schwartz M S; Weber R J; Kent W J; Karolchik D; Bruen T C; Bevan R; Cutler D J; Schwartz S; Elnitski L; Idol J R; Prasad A B; Lee-Lin S-Q; Maduro V V B; Summers T J; Portnoy M E; Dietrich N L; Akhter N; Ayele K; Benjamin B; Cariaga K; Brinkley C P; Brooks S Y; Granite S; Guan X; Gupta J; Haghighi P; Ho S-L; Huang M C; Karlins E; Laric P L; Legaspi R; Lim M J; Maduro Q L; Masiello C A; Mastrian S D; McCloskey J C; Pearson R; Stantripop S; Tiongson E E; Tran J T; Tsurgeon C; Vogt J L; Walker M A; Wetherby K D; Wiggins L S; Young A C; Zhang L-H; Osoegawa K; Zhu B; Zhao B; Shu C L; De Jong P J; Lawrence C E; Smit A F; Chakravarti A; Haussler D; Green P; Miller W; Green E D
Comparative analyses of multi-species sequences from targeted genomic regions.
Nature 2003;424(6950):788-93.
2003: Zhu Xiaofeng; Chang Yen-Pei C; Yan Denise; Weder Alan; Cooper Richard; Luke Amy; Kan Donghui; Chakravarti Aravinda
Associations between hypertension and genes in the renin-angiotensin system.
Hypertension 2003;41(5):1027-34.
2003: Uhlmann Wendy R; Bennett Robin; Botkin Jeffrey R; Botstein David; Boughman Joann A; Chakravarti Aravinda; Clayton Ellen Wright; Kahn Jeffrey; Koenig Barbara; Murray Thomas H; Olson Maynard V; Rowley Janet; Terry Sharon; Valle David
Planning the genome institute's future.
Science (New York, N.Y.) 2003;299(5612):1515; author reply 1515.
2003: Weder Alan B; Delgado Maria Carolina; Zhu Xiaofeng; Gleiberman Lillian; Kan Donghui; Chakravarti Aravinda
Erythrocyte sodium-lithium countertransport and blood pressure: a genome-wide linkage study.
Hypertension 2003;41(3 Pt 2):842-6.
2003: Mitchell Adele A; Cutler David J; Chakravarti Aravinda
Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test.
American journal of human genetics 2003;72(3):598-610.
2003: Sen Srijan; Nesse Randolph M; Stoltenberg Scott F; Li Sheng; Gleiberman Lillian; Chakravarti Aravinda; Weder Alan B; Burmeister Margit
A BDNF coding variant is associated with the NEO personality inventory domain neuroticism, a risk factor for depression.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2003;28(2):397-401.
2003: McCallion Andrew S; Stames Erine; Conlon Ronald A; Chakravarti Aravinda
Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(4):1826-31.
2003: Zhu Xiaofeng; Yan Denise; Cooper Richard S; Luke Amy; Ikeda Morna A; Chang Yen-Pei C; Weder Alan; Chakravarti Aravinda
Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program.
Genome research 2003;13(2):173-81.
2003: Thiel Bonnie A; Chakravarti Aravinda; Cooper Richard S; Luke Amy; Lewis Sue; Lynn Audrey; Tiwari Hemant; Schork Nicholas J; Weder Alan B
A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans.
American journal of hypertension 2003;16(2):151-3.
2003: Chakravarti Aravinda; Little Peter
Nature, nurture and human disease.
Nature 2003;421(6921):412-4.
2003: Marth Gabor; Schuler Greg; Yeh Raymond; Davenport Ruth; Agarwala Richa; Church Deanna; Wheelan Sarah; Baker Jonathan; Ward Ming; Kholodov Michael; Phan Lon; Czabarka Eva; Murvai Janos; Cutler David; Wooding Stephen; Rogers Alan; Chakravarti Aravinda; Harpending Henry C; Kwok Pui-Yan; Sherry Stephen T
Sequence variations in the public human genome data reflect a bottlenecked population history.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(1):376-81.
2003: McCallion A S; Emison E S; Kashuk C S; Bush R T; Kenton M; Carrasquillo M M; Jones K W; Kennedy G C; Portnoy M E; Green E D; Chakravarti A
Genomic variation in multigenic traits: Hirschsprung disease.
Cold Spring Harbor symposia on quantitative biology 2003;68():373-81.
2002: Lin Shin; Cutler David J; Zwick Michael E; Chakravarti Aravinda
Haplotype inference in random population samples.
American journal of human genetics 2002;71(5):1129-37.
2002: Carrasquillo Minerva M; McCallion Andrew S; Puffenberger Erik G; Kashuk Carl S; Nouri Nassim; Chakravarti Aravinda
Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.
Nature genetics 2002;32(2):237-44.
2002: Merikangas Kathleen R; Chakravarti Aravinda; Moldin Steven O; Araj Houmam; Blangero John C; Burmeister Margit; Crabbe John; Depaulo J Raymond; Foulks Edward; Freimer Nelson B; Koretz Doreen S; Lichtenstein William; Mignot Emmanuel; Reiss Allan L; Risch Neil J; Takahashi Joseph S
Future of genetics of mood disorders research.
Biological psychiatry 2002;52(6):457-77.
2002: Christian Susan L; McDonough Jennifer; Liu Cy Chun-yu; Shaikh Sanober; Vlamakis Vivian; Badner Judith A; Chakravarti Aravinda; Gershon Elliot S
An evaluation of the assembly of an approximately 15-Mb region on human chromosome 13q32-q33 linked to bipolar disorder and schizophrenia.
Genomics 2002;79(5):635-56.
2002: Gabriel Stacey B; Salomon Rémi; Pelet Anna; Angrist Misha; Amiel Jeanne; Fornage Myriam; Attié-Bitach Tania; Olson Jane M; Hofstra Robert; Buys Charles; Steffann Julie; Munnich Arnold; Lyonnet Stanislas; Chakravarti Aravinda
Segregation at three loci explains familial and population risk in Hirschsprung disease.
Nature genetics 2002;31(1):89-93.
2002: Chakravarti Aravinda
A compelling genetic hypothesis for a complex disease: PRODH2/DGCR6 variation leads to schizophrenia susceptibility.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(8):4755-6.
2002: Marshall Donald G; Meier-Ruge W A; Chakravarti Aravinda; Langer Jacob C
Chronic constipation due to Hirschsprung's disease and desmosis coli in a family.
Pediatric surgery international 2002;18(2-3):110-4.
2002: Nath Swapan K; Chakravarti Aravinda; Chen Chien-Hsiun; Cooper Richard; Weder Alan; Schork Nicholas J
Segregation analysis of blood pressure and body mass index in a rural US community.
Human biology; an international record of research 2002;74(1):11-23.
2002: Blagoev Blagoy; Nielsen Mogens M; Angrist Misha; Chakravarti Aravinda; Pandey Akhilesh
Cloning of rat thymic stromal lymphopoietin receptor (TSLPR) and characterization of genomic structure of murine Tslpr gene.
Gene 2002;284(1-2):161-8.
2002: Weese-Mayer Debra E; Bolk Stacey; Silvestri Jean M; Chakravarti Aravinda
Idiopathic congenital central hypoventilation syndrome: evaluation of brain-derived neurotrophic factor genomic DNA sequence variation.
American journal of medical genetics 2002;107(4):306-10.
2002: Kashuk Carl; SenGupta Sanghamitra; Eichler Evan; Chakravarti Aravinda
ViewGene: a graphical tool for polymorphism visualization and characterization.
Genome research 2002;12(2):333-8.
2002: Zhu Xiaofeng; Cooper Richard S; Luke Amy; Chen Guanjie; Wu Xiaodong; Kan Donghui; Chakravarti Aravinda; Weder Alan
A genome-wide scan for obesity in African-Americans.
Diabetes 2002;51(2):541-4.
2001: Cutler D J; Zwick M E; Carrasquillo M M; Yohn C T; Tobin K P; Kashuk C; Mathews D J; Shah N A; Eichler E E; Warrington J A; Chakravarti A
High-throughput variation detection and genotyping using microarrays.
Genome research 2001;11(11):1913-25.
2001: Mathews D J; Kashuk C; Brightwell G; Eichler E E; Chakravarti A
Sequence variation within the fragile X locus.
Genome research 2001;11(8):1382-91.
2001: McCallion A S; Chakravarti A
EDNRB/EDN3 and Hirschsprung disease type II.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 2001;14(3):161-9.
2001: Chakravarti A
Statistical analysis of radiation hybrid data.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 3():Unit 3.4.
2001: Green E D; Chakravarti A
The human genome sequence expedition: views from the "base camp".
Genome research 2001;11(5):645-51.
2001: Hong H K; Noveroske J K; Headon D J; Liu T; Sy M S; Justice M J; Chakravarti A
The winged helix/forkhead transcription factor Foxq1 regulates differentiation of hair in satin mice.
Genesis (New York, N.Y. : 2000) 2001;29(4):163-71.
2001: Wiesner G L; Platzer P; Buxbaum S; Lewis S; MacMillen M; Olechnowicz J; Willis J; Chakravarti A; Elston R C; Markowitz S D
Testing for colon neoplasia susceptibility variants at the human COX2 locus.
Journal of the National Cancer Institute 2001;93(8):635-9.
2001: Chakravarti A
To a future of genetic medicine.
Nature 2001;409(6822):822-3.
2001: Chatterjee S K; Banerjee S; Basak D; Basu A K; Chakravarti A K; Chatterjee U S; Haque J
Posterior urethral valves: the scenario in a developing center.
Pediatric surgery international 2001;17(1):2-7.
2000: Schork N J; Nath S K; Fallin D; Chakravarti A
Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects.
American journal of human genetics 2000;67(5):1208-18.
2000: Lynn A; Kashuk C; Petersen M B; Bailey J A; Cox D R; Antonarakis S E; Chakravarti A
Patterns of meiotic recombination on the long arm of human chromosome 21.
Genome research 2000;10(9):1319-32.
2000: Province M A; Boerwinkle E; Chakravarti A; Cooper R; Fornage M; Leppert M; Risch N; Ranade K
Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. National Heart, Lung and Blood Institute.
Journal of hypertension 2000;18(7):867-76.
2000: Schork N J; Chakravarti A; Thiel B; Fornage M; Jacob H J; Cai R; Rotimi C N; Cooper R S; Weder A B
Lack of association between a biallelic polymorphism in the adducin gene and blood pressure in whites and African Americans.
American journal of hypertension 2000;13(6 Pt 1):693-8.
2000: Fan J B; Chen X; Halushka M K; Berno A; Huang X; Ryder T; Lipshutz R J; Lockhart D J; Chakravarti A
Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays.
Genome research 2000;10(6):853-60.
2000: Bailey J A; Carrel L; Chakravarti A; Eichler E E
Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(12):6634-9.
2000: Zaragoza M V; Surti U; Redline R W; Millie E; Chakravarti A; Hassold T J
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole.
American journal of human genetics 2000;66(6):1807-20.
2000: Bolk S; Pelet A; Hofstra R M; Angrist M; Salomon R; Croaker D; Buys C H; Lyonnet S; Chakravarti A
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(1):268-73.
2000: Zwick M E; Cutler D J; Chakravarti A
Patterns of genetic variation in Mendelian and complex traits.
Annual review of genomics and human genetics 2000;1():387-407.
1999: Bolk S; Puffenberger E G; Hudson J; Morton D H; Chakravarti A
Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites.
American journal of human genetics 1999;65(6):1785-90.
1999: Halushka M K; Mathews D J; Bailey J A; Chakravarti A
GIST: A web tool for collecting gene information.
Physiological genomics 1999;1(2):75-81.
1999: Jönsson E G; Nimgaonkar V L; Zhang X R; Shaw S H; Burgert E; Crocq M A; Chakravarti A; Sedvall G C
Trend for an association between schizophrenia and D3S1310, a marker in proximity to the dopamine D3 receptor gene.
American journal of medical genetics 1999;88(4):352-7.
1999: Halushka M K; Fan J B; Bentley K; Hsie L; Shen N; Weder A; Cooper R; Lipshutz R; Chakravarti A
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis.
Nature genetics 1999;22(3):239-47.
1999: Hong H K; Lass J H; Chakravarti A
Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene.
Human molecular genetics 1999;8(4):625-37.
1999: Southard-Smith E M; Angrist M; Ellison J S; Agarwala R; Baxevanis A D; Chakravarti A; Pavan W J
The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.
Genome research 1999;9(3):215-25.
1999: Kibar Z; Lafrenière R G; Chakravarti A; Wang J C; Chevrette M; Der Kaloustian V M; Rouleau G A
A radiation hybrid map of 48 loci including the clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q.
Genomics 1999;56(1):127-30.
1999: Chakravarti A
1998 ASHG Award for Excellence in Education. Professor Ching Chun Li, courageous scholar and educator.
American journal of human genetics 1999;64(1):14-5.
1999: Chakravarti A
Population genetics--making sense out of sequence.
Nature genetics 1999;21(1 Suppl):56-60.
1998: Angrist M; Bolk S; Bentley K; Nallasamy S; Halushka M K; Chakravarti A
Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease.
Oncogene 1998;17(23):3065-70.
1998: Collins F S; Brooks L D; Chakravarti A
A DNA polymorphism discovery resource for research on human genetic variation.
Genome research 1998;8(12):1229-31.
1998: Collins F S; Patrinos A; Jordan E; Chakravarti A; Gesteland R; Walters L
New goals for the U.S. Human Genome Project: 1998-2003.
Science (New York, N.Y.) 1998;282(5389):682-9.
1998: Blouin J L; Dombroski B A; Nath S K; Lasseter V K; Wolyniec P S; Nestadt G; Thornquist M; Ullrich G; McGrath J; Kasch L; Lamacz M; Thomas M G; Gehrig C; Radhakrishna U; Snyder S E; Balk K G; Neufeld K; Swartz K L; DeMarchi N; Papadimitriou G N; Dikeos D G; Stefanis C N; Chakravarti A; Childs B; Housman D E; Kazazian H H; Antonarakis S; Pulver A E
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21.
Nature genetics 1998;20(1):70-3.
1998: Potier M; Dutriaux A; Orti R; Groet J; Gibelin N; Karadima G; Lutfalla G; Lynn A; Van Broeckhoven C; Chakravarti A; Petersen M; Nizetic D; Delabar J; Rossier J
Two sequence-ready contigs spanning the two copies of a 200-kb duplication on human 21q: partial sequence and polymorphisms.
Genomics 1998;51(3):417-26.
1998: Chakravarti A
It's raining SNPs, hallelujah?
Nature genetics 1998;19(3):216-7.
1998: Brown D M; Matise T C; Koike G; Simon J S; Winer E S; Zangen S; McLaughlin M G; Shiozawa M; Atkinson O S; Hudson J R; Chakravarti A; Lander E S; Jacob H J
An integrated genetic linkage map of the laboratory rat.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(7):521-30.
1998: Angrist M; Jing S; Bolk S; Bentley K; Nallasamy S; Halushka M; Fox G M; Chakravarti A
Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.
Genomics 1998;48(3):354-62.
1998: Shaw S H; Carrasquillo M M; Kashuk C; Puffenberger E G; Chakravarti A
Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes.
Genome research 1998;8(2):111-23.
1998: Chadwick B P; Helbling L A; Angrist M; Chakravarti A; Gusella J F; Slaugenhaupt S A
Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR.
Cytogenetics and cell genetics 1998;83(3-4):236-7.
1997: Carrasquillo M M; Zlotogora J; Barges S; Chakravarti A
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
Human molecular genetics 1997;6(12):2163-72.
1997: Petersen M B; Tomasetto C; Lynn A; Chakravarti A
A PvuII polymorphism detected by a cDNA clone of the gene encoding the human spasmolytic protein protein (SML1 gene), one of three members of the trefoil peptide gene family clustered on chromosome 21q22.3.
Clinical genetics 1997;52(4):247-8.
1997: Chen H; Rossier C; Nakamura Y; Lynn A; Chakravarti A; Antonarakis S E
Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3.
Genomics 1997;41(2):193-200.
1996: Nimgaonkar V L; Sanders A R; Ganguli R; Zhang X R; Brar J; Hogge W; Fann W E; Patel P I; Chakravarti A
Association study of schizophrenia and the dopamine D3 receptor gene locus in two independent samples.
American journal of medical genetics 1996;67(6):505-14.
1996: Angrist M; Bolk S; Halushka M; Lapchak P A; Chakravarti A
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
Nature genetics 1996;14(3):341-4.
1996: Cohen T; Zeitune M; McGillivray B C; Hall J G; Lynn A H; Aston C E; Chakravarti A
Segregation analysis of microcephaly.
American journal of medical genetics 1996;65(3):226-34.
1996: Boguski M; Chakravarti A; Gibbs R; Green E; Myers R M
The end of the beginning: the race to begin human genome sequencing.
Genome research 1996;6(9):771-2.
1996: Bolk S; Angrist M; Xie J; Yanagisawa M; Silvestri J M; Weese-Mayer D E; Chakravarti A
Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome.
Nature genetics 1996;13(4):395-6.
1996: Chen H; Rossier C; Lalioti M D; Lynn A; Chakravarti A; Perrin G; Antonarakis S E
Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3.
American journal of human genetics 1996;59(1):66-75.
1996: Kwoh C K; Venglish C; Lynn A H; Whitley D M; Young E; Chakravarti A
Age, sex, and the familial risk of rheumatoid arthritis.
American journal of epidemiology 1996;144(1):15-24.
1996: Bolk S; Angrist M; Schwartz S; Silvestri J M; Weese-Mayer D E; Chakravarti A
Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.
American journal of medical genetics 1996;63(4):603-9.
1996: Hofstra R M; Osinga J; Tan-Sindhunata G; Wu Y; Kamsteeg E J; Stulp R P; van Ravenswaaij-Arts C; Majoor-Krakauer D; Angrist M; Chakravarti A; Meijers C; Buys C H
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).
Nature genetics 1996;12(4):445-7.
1996: Eichler E E; Macpherson J N; Murray A; Jacobs P A; Chakravarti A; Nelson D L
Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.
Human molecular genetics 1996;5(3):319-30.
1996: Chakravarti A
Endothelin receptor-mediated signaling in hirschsprung disease.
Human molecular genetics 1996;5(3):303-7.
1995: Angrist M; Wells D E; Chakravarti A; Pandey A
Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA.
Genomics 1995;30(3):623-5.
1995: Chakravarti A
The CD4/CD8 ratio: message in a bottle?
Nature medicine 1995;1(12):1240-1.
1995: Nimgaonkar V L; Yang Z W; Zhang X R; Brar J S; Chakravarti A; Ganguli R
Association study of schizophrenia and the IL-2 receptor beta chain gene.
American journal of medical genetics 1995;60(5):448-51.
1995: Blouin J L; Christie D H; Gos A; Lynn A; Morris M A; Ledbetter D H; Chakravarti A; Antonarakis S E
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.
American journal of human genetics 1995;57(2):388-94.
1995: Talbot C C; Avramopoulos D; Gerken S; Chakravarti A; Armour J A; Matsunami N; White R; Antonarakis S E
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells.
Human molecular genetics 1995;4(7):1193-9.
1995: Christian S L; Robinson W P; Huang B; Mutirangura A; Line M R; Nakao M; Surti U; Chakravarti A; Ledbetter D H
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.
American journal of human genetics 1995;57(1):40-8.
1995: Lynn A H; Kwoh C K; Venglish C M; Aston C E; Chakravarti A
Genetic epidemiology of rheumatoid arthritis.
American journal of human genetics 1995;57(1):150-9.
1995: Angrist M; Bolk S; Thiel B; Puffenberger E G; Hofstra R M; Buys C H; Cass D T; Chakravarti A
Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.
Human molecular genetics 1995;4(5):821-30.
1995: Scott J A; Wenger S L; Steele M W; Chakravarti A
Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.
American journal of medical genetics 1995;56(1):67-71.
1995: Washington S S; Warburton D; Chakravarti A
Report and abstracts of the Second International Workshop on Human Chromosome 13 Mapping 1994.
Cytogenetics and cell genetics 1995;70(1-2):1-22.
1994: Chakravarti A
The behavior of meiosis in sperm.
American journal of human genetics 1994;55(3):421-2.
1994: Matise T C; Chakravarti A; Patel P I; Lupski J R; Nelis E; Timmerman V; Van Broeckhoven C; Weeks D E
Detection of tandem duplications and implications for linkage analysis.
American journal of human genetics 1994;54(6):1110-21.
1994: Hoffner L; Deka R; Chakravarti A; Surti U
Cytogenetics and origins of pediatric germ cell tumors.
Cancer genetics and cytogenetics 1994;74(1):54-8.
1994: Matise T C; Perlin M; Chakravarti A
Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map.
Nature genetics 1994;6(4):384-90.
1994: Li C C; Chakravarti A
DNA profile similarity in a subdivided population.
Human heredity 1994;44(2):100-9.
1994: Zappata S; Petersen M B; König U; Blaschak J; Chakravarti A; Tassone F; Serra A; Antonarakis S E; Brahe C
Highly polymorphic repeat marker within the beta-amyloid precursor protein gene.
Human genetics 1994;93(1):85-6.
1994: Samec S; Clarkson S G; Blaschak J; Chakravarti A; Morris M A; Scherly D; Antonarakis S E
Dinucleotide repeat polymorphism within ERCC5 gene.
Human molecular genetics 1994;3(1):214.
1993: Delabar J M; Créau N; Sinet P M; Ritter O; Antonarakis S E; Burmeister M; Chakravarti A; Nizetic D; Ohki M; Patterson D
Report of the Fourth International Workshop on Human Chromosome 21.
Genomics 1993;18(3):735-45.
1993: Washington S S; Bowcock A M; Gerken S; Matsunami N; Lesh D; Osborne-Lawrence S L; Cowell J; Ledbetter D H; White R L; Chakravarti A
A somatic cell hybrid map of human chromosome 13.
Genomics 1993;18(3):486-95.
1993: Nimgaonkar V L; Zhang X R; Caldwell J G; Ganguli R; Chakravarti A
Association study of schizophrenia with dopamine D3 receptor gene polymorphisms: probable effects of family history of schizophrenia?
American journal of medical genetics 1993;48(4):214-7.
1993: Perlin M; Chakravarti A
Efficient construction of high-resolution physical maps from yeast artificial chromosomes using radiation hybrids: inner product mapping.
Genomics 1993;18(2):283-9.
1993: Nimgaonkar V L; Scott J A; Brar J S; Ganguli R; Chakravarti A
Co-occurrence of schizophrenia and Treacher Collins syndrome.
American journal of medical genetics 1993;48(3):156-8.
1993: Winokur S T; Schutte B; Weiffenbach B; Washington S S; McElligott D; Chakravarti A; Wasmuth J H; Altherr M R
A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).
American journal of human genetics 1993;53(4):874-80.
1993: Hong H K; Giorda R; Trucco M; Chakravarti A
Dinucleotide repeat polymorphism at the DXS1146 locus.
Human molecular genetics 1993;2(7):1078.
1993: McInnis M G; Chakravarti A; Blaschak J; Petersen M B; Sharma V; Avramopoulos D; Blouin J L; König U; Brahe C; Matise T C
A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM.
Genomics 1993;16(3):562-71.
1993: Hong H K; Giorda R; Yu L M; Trucco M; Chakravarti A
Microsatellite repeat polymorphism at the D13S197 locus.
Human molecular genetics 1993;2(3):337.
1993: Warren A C; McInnis M G; Kalaitsidaki M; Cox T K; Blaschak J; Chakravarti A; Antonarakis S E
D21S210: a highly polymorphic (GT)n marker closely linked to the beta-amyloid protein precursor (APP) gene.
Human genetics 1993;91(1):87-8.
1993: Mutirangura A; Greenberg F; Butler M G; Malcolm S; Nicholls R D; Chakravarti A; Ledbetter D H
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.
Human molecular genetics 1993;2(2):143-51.
1993: Bowcock A; Osborne-Lawrence S; Barnes R; Chakravarti A; Washington S; Dunn C
Microsatellite polymorphism linkage map of human chromosome 13q.
Genomics 1993;15(2):376-86.
1993: Li C C; Weeks D E; Chakravarti A
Similarity of DNA fingerprints due to chance and relatedness.
Human heredity 1993;43(1):45-52.
1993: Hong H K; Giorda R; Trucco M; Chakravarti A
Dinucleotide repeat polymorphisms at the D13S192 and D13S193 loci.
Human molecular genetics 1993;2(1):86.
1993: Avramopoulos D; Chakravarti A; Antonarakis S E
DNA polymorphisms in the 3' untranslated region of genes on human chromosome 21.
Genomics 1993;15(1):98-102.
1993: Avramopoulos D; Cox T; Kraus J P; Chakravarti A; Antonarakis S E
Linkage mapping of the cystathionine beta-synthase (CBS) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region.
Human genetics 1993;90(5):566-8.
1993: Matise T C; Perlin M; Chakravarti A
MultiMap: an expert system for automated genetic linkage mapping.
Proceedings / ... International Conference on Intelligent Systems for Molecular Biology ; ISMB. International Conference on Intelligent Systems for Molecular Biology 1993;1():260-5.
1992: Kalaitsidaki M; Cox T; Chakravarti A; Antonarakis S E
Cloning and linkage mapping of three polymorphic tetranucleotide (TAAA)n repeats on human chromosome 21.
Genomics 1992;14(4):1071-5.
1992: Warren A C; McInnis M G; Blaschak J; Kaliatsidaki M; Petersen M B; Chakravarti A; Antonarakis S E
Dinucleotide repeat (GT)n markers on chromosome 21.
Genomics 1992;14(3):818-9.
1992: Avramopoulos D; Cox T; Blaschak J E; Chakravarti A; Antonarakis S E
Linkage mapping of the AML1 gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region.
Genomics 1992;14(2):506-7.
1992: Nimgaonkar V L; Ganguli R; Washington S S; Chakravarti A
Schizophrenia and porphobilinogen deaminase gene polymorphisms: an association study.
Schizophrenia research 1992;8(1):51-8.
1992: Peterson M B; Frantzen M; Antonarakis S E; Warren A C; Van Broeckhoven C; Chakravarti A; Cox T K; Lund C; Olsen B; Poulsen H
Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.
American journal of human genetics 1992;51(3):516-25.
1992: Hoffner L; Shen-Schwarz S; Deka R; Chakravarti A; Surti U
Genetics and biology of human ovarian teratomas. III. Cytogenetics and origins of malignant ovarian germ cell tumors.
Cancer genetics and cytogenetics 1992;62(1):58-65.
1992: Warren A C; Petersen M B; Van Hul W; McInnis M G; Van Broeckhoven C; Cox T K; Chakravarti A; Antonarakis S E
D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21.
Genomics 1992;13(4):1365-7.
1992: Chakravarti A
Fragile X founder effect?
Nature genetics 1992;1(4):237-8.
1992: Avramopoulos D; Cox T; Forrest G L; Chakravarti A; Antonarakis S E
Linkage mapping of the carbonyl reductase (CBR) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region.
Genomics 1992;13(2):447-8.
1992: Spielvogel H; Hennies H C; Claussen U; Washington S S; Chakravarti A; Reis A
Band-specific localization of the microsatellite at D13S71 by microdissection and enzymatic amplification.
American journal of human genetics 1992;50(5):1031-7.
1992: Chakravarti A; Reefer J E
A theory for radiation hybrid (Goss-Harris) mapping: application to proximal 21q markers.
Cytogenetics and cell genetics 1992;59(2-3):99-101.
1992: Aston C E; Chakravarti A
The gene order problem when using somatic cell hybrids.
Cytogenetics and cell genetics 1992;59(2-3):90-2.
1992: Warren A C; Antonarakis S E; Chakravarti A
Chromosome 21 genetic linkage data set based on CEPH pedigrees.
Cytogenetics and cell genetics 1992;59(2-3):86-7.
1991: McInnis M G; Lutfalla G; Slaugenhaupt S; Petersen M B; Uze G; Chakravarti A; Antonarakis S E
Linkage mapping of highly informative DNA polymorphisms within the human interferon-alpha receptor gene on chromosome 21.
Genomics 1991;11(3):573-6.
1991: Chakravarti A
Information content of the Centre d'Etude du Polymorphisme Humain (CEPH) family structures for linkage studies.
Human genetics 1991;87(6):721-4.
1991: Chakravarti A
A graphical representation of genetic and physical maps: the Marey map.
Genomics 1991;11(1):219-22.
1991: Petersen M B; Weber J L; Slaugenhaupt S A; Kwitek A E; McInnis M G; Chakravarti A; Antonarakis S E
Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat.
Human genetics 1991;87(4):401-4.
1991: Lupski J R; de Oca-Luna R M; Slaugenhaupt S; Pentao L; Guzzetta V; Trask B J; Saucedo-Cardenas O; Barker D F; Killian J M; Garcia C A; Chakravarti A; Patel P I
DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
Cell 1991;66(2):219-32.
1991: Chakravarti A; Lasher L K; Reefer J E
A maximum likelihood method for estimating genome length using genetic linkage data.
Genetics 1991;128(1):175-82.
1991: Keats B J; Sherman S L; Morton N E; Robson E B; Buetow K H; Cartwright P E; Chakravarti A; Francke U; Green P P; Ott J
Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990).
Genomics 1991;9(3):557-60.
1991: Petersen M B; Slaugenhaupt S A; Lewis J G; Warren A C; Chakravarti A; Antonarakis S E
A genetic linkage map of 27 markers on human chromosome 21.
Genomics 1991;9(3):407-19.
1991: Morizot D C; Slaugenhaupt S A; Kallman K D; Chakravarti A
Genetic linkage map of fishes of the genus Xiphophorus (Teleostei: Poeciliidae).
Genetics 1991;127(2):399-410.
1991: Keats B J; Sherman S L; Morton N E; Robson E B; Buetow K H; Cartwright P E; Chakravarti A; Francke U; Green P P; Ott J
Guidelines for human linkage maps. An International System for Human Linkage Maps (ISLM, 1990).
Annals of human genetics 1991;55(Pt 1):1-6.
1990: Patel P I; Garcia C; Montes de Oca-Luna R; Malamut R I; Franco B; Slaugenhaupt S; Chakravarti A; Lupski J R
Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids.
American journal of human genetics 1990;47(6):926-34.
1990: Surti U; Hoffner L; Chakravarti A; Ferrell R E
Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin.
American journal of human genetics 1990;47(4):635-43.
1990: Lewis J G; Weber J L; Petersen M B; Slaugenhaupt S A; Kwitek A; May P E; Warren A C; Chakravarti A; Antonarakis S E
Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat.
Genomics 1990;8(2):400-2.
1990: Deka R; Chakravarti A; Surti U; Hauselman E; Reefer J; Majumder P P; Ferrell R E
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers.
American journal of human genetics 1990;47(4):644-55.
1990: Neiswanger K; Slaugenhaupt S A; Hughes H B; Frank E; Frankel D R; McCarty M J; Chakravarti A; Zubenko G S; Kupfer D J; Kaplan B B
Evidence against close linkage of unipolar affective illness to human chromosome 11p markers HRAS1 and INS and chromosome Xq marker DXS52.
Biological psychiatry 1990;28(1):63-72.
1990: Petersen M B; Economou E P; Slaugenhaupt S A; Chakravarti A; Antonarakis S E
Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker.
Genomics 1990;7(1):136-8.
1990: Patel P I; Franco B; Garcia C; Slaugenhaupt S A; Nakamura Y; Ledbetter D H; Chakravarti A; Lupski J R
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.
American journal of human genetics 1990;46(4):801-9.
1990: Badner J A; Sieber W K; Garver K L; Chakravarti A
A genetic study of Hirschsprung disease.
American journal of human genetics 1990;46(3):568-80.
1990: Badner J A; Chakravarti A
Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene.
American journal of medical genetics 1990;35(1):100-4.
1990: Long J C; Chakravarti A; Boehm C D; Antonarakis S; Kazazian H H
Phylogeny of human beta-globin haplotypes and its implications for recent human evolution.
American journal of physical anthropology 1990;81(1):113-30.
1989: Kerem B; Rommens J M; Buchanan J A; Markiewicz D; Cox T K; Chakravarti A; Buchwald M; Tsui L C
Identification of the cystic fibrosis gene: genetic analysis.
Science (New York, N.Y.) 1989;245(4922):1073-80.
1989: Chakravarti A; Slaugenhaupt S A; Zubenko G S
Inheritance pattern of platelet membrane fluidity in Alzheimer disease.
American journal of human genetics 1989;44(6):799-805.
1989: Chakravarti A
The probability of detecting the origin of nondisjunction of autosomal trisomies.
American journal of human genetics 1989;44(5):639-45.
1989: Warren A C; Slaugenhaupt S A; Lewis J G; Chakravarti A; Antonarakis S E
A genetic linkage map of 17 markers on human chromosome 21.
Genomics 1989;4(4):579-91.
1989: Leitersdorf E; Chakravarti A; Hobbs H H
Polymorphic DNA haplotypes at the LDL receptor locus.
American journal of human genetics 1989;44(3):409-21.
1989: Kittur S D; Bagdon M M; Lubs M L; Phillips J A; Murray J C; Slaugenhaupt S A; Chakravarti A; Adler W H
Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers.
American journal of human genetics 1989;44(1):48-50.
1989: Chakravarti A; Majumder P P; Slaugenhaupt S A; Deka R; Warren A C; Surti U; Ferrell R E; Antonarakis S E
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas.
Progress in clinical and biological research 1989;311():45-79.
1989: Antonarakis S E; Warren A C; McCormick M K; Lewis J G; Hieter P A; Chakravarti A
Molecular mapping of chromosome 21 and the region responsible for Down syndrome.
Progress in clinical and biological research 1989;311():29-43.
1988: Antonarakis S E; Oettgen P; Chakravarti A; Halloran S L; Hudson R R; Feisee L; Karathanasis S K
DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster.
Human genetics 1988;80(3):265-73.
1988: Cramer D V; Chakravarti A; Arenas O; Humprieres J; Mowery P A
Genetic diversity within and between natural populations of Rattus norvegicus.
The Journal of heredity 1988;79(5):319-24.
1988: Li C C; Chakravarti A
An expository review of two methods of calculating the paternity probability.
American journal of human genetics 1988;43(2):197-205.
1988: Huff F J; Auerbach J; Chakravarti A; Boller F
Risk of dementia in relatives of patients with Alzheimer's disease.
Neurology 1988;38(5):786-90.
1988: Murray J C; Buetow K H; Smith M; Carlock L; Chakravarti A; Ferrell R F; Gedamu L; Gilliam C; Shiang R; DeHaven C R
Pairwise linkage analysis of 11 loci on human chromosome 4.
American journal of human genetics 1988;42(3):490-7.
1988: Chatterjee S K; Chakravarti A K; Deb Maulik T K; De Majumdar N; Sen M K
Staging the separation of ischiopagus twins.
Journal of pediatric surgery 1988;23(1 Pt 2):73-5.
1988: Chidambaram A; Chakravarti A; Ferrell R E; Iyengar S
Estimating the age-at-onset function using life-table methods.
Genetic epidemiology 1988;5(4):255-63.
1987: Chakravarti A; Slaugenhaupt S A
Methods for studying recombination on chromosomes that undergo nondisjunction.
Genomics 1987;1(1):35-42.
1987: Halloran S L; Chakravarti A
DSLINK: a computer program for gene-centromere linkage analysis in families with a trisomic offspring.
American journal of human genetics 1987;41(3):350-5.
1987: Kittur S; Lubs M L; Bauer M; Chakravarti A; Kazazian H
Linkage analysis of neurofibromatosis.
Journal of medical genetics 1987;24(9):526-7.
1987: Buetow K H; Chakravarti A
Multipoint gene mapping using seriation. II. Analysis of simulated and empirical data.
American journal of human genetics 1987;41(2):189-201.
1987: Buetow K H; Chakravarti A
Multipoint gene mapping using seriation. I. General methods.
American journal of human genetics 1987;41(2):180-8.
1987: Warren A C; Chakravarti A; Wong C; Slaugenhaupt S A; Halloran S L; Watkins P C; Metaxotou C; Antonarakis S E
Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome.
Science (New York, N.Y.) 1987;237(4815):652-4.
1987: Chakravarti A; Badner J A; Li C C
Tests of linkage and heterogeneity in Mendelian diseases using identity by descent scores.
Genetic epidemiology 1987;4(4):255-66.
1987: Li C C; Chakravarti A; Halloran S L
Estimation of segregation and ascertainment probabilities by discarding the single probands.
Genetic epidemiology 1987;4(3):185-91.
1986: Bale S J; Chakravarti A; Greene M H
Cutaneous malignant melanoma and familial dysplastic nevi: evidence for autosomal dominance and pleiotropy.
American journal of human genetics 1986;38(2):188-96.
1986: Chakravarti A; Elbein S C; Permutt M A
Evidence for increased recombination near the human insulin gene: implication for disease association studies.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(4):1045-9.
1986: Chakravarti A; Halloran S L; Bale S J; Tucker M A
Etiological heterogeneity in Hodgkin's disease: HLA linked and unlinked determinants of susceptibility independent of histological concordance.
Genetic epidemiology 1986;3(6):407-15.
1986: Buetow K H; Chakravarti A; Cole S A
A genetic map of human chromosome 11p.
Genetic epidemiology. Supplement 1986;1():135-40.
1986: Antonarakis S E; Chakravarti A; Warren A C; Slaugenhaupt S A; Wong C; Halloran S L; Metaxotou C
Reduced recombination rate on chromosomes 21 that have undergone nondisjunction.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():185-90.
1986: Badner J A; Chakravarti A; Buetow K H
Linkage analysis between Huntington disease and the G8 marker locus.
Genetic epidemiology. Supplement 1986;1():211-6.
1985: Kittur S D; Antonarakis S E; Tanzi R E; Meyers D A; Chakravarti A; Groner Y; Phillips J A; Watkins P C; Gusella J F; Kazazian H H
A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21.
The EMBO journal 1985;4(9):2257-60.
1985: Chakravarti A; Buetow K H
A strategy for using multiple linked markers for genetic counseling.
American journal of human genetics 1985;37(5):984-97.
1985: Li C C; Chakravarti A
Basic fallacies in the formulation of the paternity index.
American journal of human genetics 1985;37(4):809-18.
1985: Matteson K J; Ostrer H; Chakravarti A; Buetow K H; O'Brien W E; Beaudet A L; Phillips J A
A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locus.
Human genetics 1985;69(3):263-7.
1984: Chakravarti A; Buetow K H; Antonarakis S E; Waber P G; Boehm C D; Kazazian H H
Nonuniform recombination within the human beta-globin gene cluster.
American journal of human genetics 1984;36(6):1239-58.
1984: Chakravarti A; Phillips J A; Mellits K H; Buetow K H; Seeburg P H
Patterns of polymorphism and linkage disequilibrium suggest independent origins of the human growth hormone gene cluster.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(19):6085-9.
1984: Bale S J; Chakravarti A; Ferrell R E; Spence M A
Possible heterogeneity in the phosphoglycolate phosphatase (PGP)-haptoglobin alpha (HPA) linkage.
American journal of human genetics 1984;36(4):808-14.
1984: Chakravarti A; Li C C
Estimating the prior probability of paternity from the results of exclusion tests.
Forensic science international 1984;24(2):143-7.
1984: Chakravarti A; Li C C; Buetow K H
Estimation of the marker gene frequency and linkage disequilibrium from conditional marker data.
American journal of human genetics 1984;36(1):177-86.
1984: Badner J A; Chakravarti A; Wagener D K
A test of nonrandom segregation.
Genetic epidemiology 1984;1(4):329-40.
1984: Chakravarti A
Aspects of linkage analysis using RFLP's.
Progress in clinical and biological research 1984;147():293-5.
1984: Bale S J; Chakravarti A; Strong L C
Aggregation of colon cancer in family data.
Genetic epidemiology 1984;1(1):53-61.
1983: Chakravarti A; Bale S J
Differences in the frequency of X-linked deleterious genes in human populations.
American journal of human genetics 1983;35(6):1252-7.
1983: Chakravarti A; Li C C
The probability of exclusion based on the HLA locus.
American journal of human genetics 1983;35(5):1048-52.
1983: Lebo R V; Chakravarti A; Buetow K H; Cheung M C; Cann H; Cordell B; Goodman H
Recombination within and between the human insulin and beta-globin gene loci.
Proceedings of the National Academy of Sciences of the United States of America 1983;80(15):4808-12.
1983: Chakravarti A
Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium.
American journal of human genetics 1983;35(4):592-610.
1983: Daiger S P; Chakravarti A
Deletion mapping of polymorphic loci by apparent parental exclusion.
American journal of medical genetics 1983;14(1):43-8.
1982: Chakravarti A; Nei M
Utility and efficiency of linked marker genes for genetic counseling. II. Identification of linkage phase by offspring phenotypes.
American journal of human genetics 1982;34(4):531-51.
1981: Ferrell R E; Hittner H M; Chakravarti A
Autosomal dominant cone-rod dystrophy: a linkage study with 17 biochemical and serological markers.
American journal of medical genetics 1981;8(3):363-9.
1980: Ferrell R E; Chakravarti A; Hittner H M; Riccardi V M
Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2.
Proceedings of the National Academy of Sciences of the United States of America 1980;77(3):1580-2.
1978: Chakravarti A; Chakraborty R
Elevated frequency of Tay-Sachs disease among Ashkenazic Jews unlikely by genetic drift alone.
American journal of human genetics 1978;30(3):256-61.
1978: Malhotra K C; Chakraborty R; Chakravarti A
Gene differentiation among the Dhangar caste-cluster of Maharashtra, India.
Human heredity 1978;28(1):26-36.
1977: Nei M; Chakravarti A
Drift variances of FST and GST statistics obtained from a finite number of isolated populations.
Theoretical population biology 1977;11(3):307-25.
1977: Nei M; Chakravarti A; Tateno Y
Mean and variance of FST in a finite number of incompletely isolated populations.
Theoretical population biology 1977;11(3):291-306.
1977: Chakraborty R; Chakravarti A; Malhotra K C
Variation in allele frequencies among caste groups of the Dhangars of Maharashtra, India: an analysis with Wright's Fst statistic.
Annals of human biology 1977;4(3):275-80.
1977: Chakraborty R; Chakravarti A
On consanguineous marriages and the genetic load.
Human genetics 1977;36(1):47-54.

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