| Year |
Citation |
Score |
| 2022 |
He KY, Kelly TN, Wang H, Liang J, Zhu L, Cade BE, Assimes TL, Becker LC, Beitelshees AL, Bielak LF, Bress AP, Brody JA, Chang YC, Chang YC, de Vries PS, ... ... Chakravarti A, et al. Rare coding variants in RCN3 are associated with blood pressure. Bmc Genomics. 23: 148. PMID 35183128 DOI: 10.1186/s12864-022-08356-4 |
0.33 |
|
| 2021 |
Chakravarti A. Magnitude of Mendelian versus complex inheritance of rare disorders. American Journal of Medical Genetics. Part A. PMID 34418293 DOI: 10.1002/ajmg.a.62463 |
0.329 |
|
| 2019 |
Kapoor A, Lee D, Zhu L, Soliman EZ, Grove ML, Boerwinkle E, Arking DE, Chakravarti A. Multiple variant enhancers modulate its cardiac gene expression and the QT interval. Proceedings of the National Academy of Sciences of the United States of America. PMID 31068470 DOI: 10.1073/Pnas.1808734116 |
0.313 |
|
| 2019 |
He KY, Li X, Kelly TN, Liang J, Cade BE, Assimes TL, Becker LC, Beitelshees AL, Bress AP, Chang YC, Chen YI, de Vries PS, Fox ER, Franceschini N, Furniss A, ... ... Chakravarti A, et al. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data. Human Genetics. PMID 30671673 DOI: 10.1007/S00439-019-01975-0 |
0.323 |
|
| 2018 |
Kraja AT, Liu C, Fetterman JL, Graff M, Have CT, Gu C, Yanek LR, Feitosa MF, Arking DE, Chasman DI, Young K, Ligthart S, Hill WD, Weiss S, Luan J, ... ... Chakravarti A, et al. Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. American Journal of Human Genetics. PMID 30595373 DOI: 10.1016/J.Ajhg.2018.12.001 |
0.352 |
|
| 2018 |
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I, Ng FL, Evangelou M, Witkowska K, Tzanis E, Hellwege JN, ... ... Chakravarti A, et al. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics. PMID 30429575 DOI: 10.1038/S41588-018-0297-3 |
0.326 |
|
| 2018 |
Wang H, Nandakumar P, Tekola-Ayele F, Tayo BO, Ware EB, Gu CC, Lu Y, Yao J, Zhao W, Smith JA, Hellwege JN, Guo X, Edwards TL, Loos RJF, Arnett DK, ... ... Chakravarti A, et al. Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31. European Journal of Human Genetics : Ejhg. PMID 30262922 DOI: 10.1038/S41431-018-0277-1 |
0.452 |
|
| 2018 |
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I, Ng FL, Evangelou M, Witkowska K, Tzanis E, Hellwege JN, ... ... Chakravarti A, et al. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics. PMID 30224653 DOI: 10.1038/S41588-018-0205-X |
0.312 |
|
| 2018 |
Ashar FN, Mitchell RN, Albert CM, Newton-Cheh C, Brody JA, Müller-Nurasyid M, Moes A, Meitinger T, Mak A, Huikuri H, Junttila MJ, Goyette P, Pulit SL, Pazoki R, Tanck MW, ... ... Chakravarti A, et al. A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. European Heart Journal. PMID 30169657 DOI: 10.1093/Eurheartj/Ehy474 |
0.549 |
|
| 2018 |
Lee D, Kapoor A, Safi A, Song L, Halushka MK, Crawford GE, Chakravarti A. Human cardiac cis-regulatory elements, their cognate transcription factors, and regulatory DNA sequence variants. Genome Research. PMID 30139769 DOI: 10.1101/Gr.234633.118 |
0.542 |
|
| 2018 |
Nandakumar P, Morrison AC, Grove ML, Boerwinkle E, Chakravarti A. Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation. Medicine. 97: e11865. PMID 30113482 DOI: 10.1097/Md.0000000000011865 |
0.379 |
|
| 2018 |
Fernández-Rhodes L, Malinowski JR, Wang Y, Tao R, Pankratz N, Jeff JM, Yoneyama S, Carty CL, Setiawan VW, Le Marchand L, Haiman C, Corbett S, Demerath E, Heiss G, Gross M, ... ... Chakravarti A, et al. The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis. Plos One. 13: e0200486. PMID 30044860 DOI: 10.1371/Journal.Pone.0200486 |
0.397 |
|
| 2018 |
Feitosa MF, Kraja AT, Chasman DI, Sung YJ, Winkler TW, Ntalla I, Guo X, Franceschini N, Cheng CY, Sim X, Vojinovic D, Marten J, Musani SK, Li C, Bentley AR, ... ... Chakravarti A, et al. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Plos One. 13: e0198166. PMID 29912962 DOI: 10.1371/Journal.Pone.0198166 |
0.36 |
|
| 2018 |
Liang J, Le TH, Velez Edwards DR, Tayo BO, Gaulton KJ, Smith JA, Lu Y, Jensen RA, Chen G, Yanek LR, Schwander K, Tajuddin SM, Sofer T, Kim W, Kayima J, ... ... Chakravarti A, et al. Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Plos Genetics. 14: e1007345. PMID 29750786 DOI: 10.1371/Journal.Pgen.1007345 |
0.375 |
|
| 2018 |
Wang TY, Lee D, Fox-Talbot K, Arking DE, Chakravarti A, Halushka MK. Cardiomyocytes have mosaic patterns of protein expression. Cardiovascular Pathology : the Official Journal of the Society For Cardiovascular Pathology. 34: 50-57. PMID 29677652 DOI: 10.1016/J.Carpath.2018.03.002 |
0.507 |
|
| 2018 |
Sung YJ, Winkler TW, de Las Fuentes L, Bentley AR, Brown MR, Kraja AT, Schwander K, Ntalla I, Guo X, Franceschini N, Lu Y, Cheng CY, Sim X, Vojinovic D, Marten J, ... ... Chakravarti A, et al. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. American Journal of Human Genetics. PMID 29455858 DOI: 10.1016/J.Ajhg.2018.01.015 |
0.414 |
|
| 2018 |
Fadista J, Lund M, Skotte L, Geller F, Nandakumar P, Chatterjee S, Matsson H, Granström AL, Wester T, Salo P, Virtanen V, Carstensen L, Bybjerg-Grauholm J, Hougaard DM, Pakarinen M, ... ... Chakravarti A, et al. Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus. European Journal of Human Genetics : Ejhg. PMID 29379196 DOI: 10.1038/s41431-017-0053-7 |
0.331 |
|
| 2017 |
Jiang Q, Liu F, Miao C, Li Q, Zhang Z, Xiao P, Su L, Yu K, Chen X, Zhang F, Chakravarti A, Li L. RET somatic mutations are underrecognized in Hirschsprung disease. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29261189 DOI: 10.1038/Gim.2017.178 |
0.348 |
|
| 2017 |
Smith JA, Zhao W, Yasutake K, August C, Ratliff SM, Faul JD, Boerwinkle E, Chakravarti A, Diez Roux AV, Gao Y, Griswold ME, Heiss G, Kardia SLR, Morrison AC, Musani SK, et al. Gene-by-Psychosocial Factor Interactions Influence Diastolic Blood Pressure in European and African Ancestry Populations: Meta-Analysis of Four Cohort Studies. International Journal of Environmental Research and Public Health. 14. PMID 29258278 DOI: 10.3390/Ijerph14121596 |
0.398 |
|
| 2017 |
Wain LV, Vaez A, Jansen R, Joehanes R, van der Most PJ, Erzurumluoglu AM, O'Reilly PF, Cabrera CP, Warren HR, Rose LM, Verwoert GC, Hottenga JJ, Strawbridge RJ, Esko T, Arking DE, ... ... Chakravarti A, et al. Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Hypertension (Dallas, Tex. : 1979). PMID 28739976 DOI: 10.1161/Hypertensionaha.117.09438 |
0.372 |
|
| 2017 |
Liang J, Le TH, Edwards DRV, Tayo BO, Gaulton KJ, Smith JA, Lu Y, Jensen RA, Chen G, Yanek LR, Schwander K, Tajuddin SM, Sofer T, Kim W, Kayima J, ... ... Chakravarti A, et al. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Plos Genetics. 13: e1006728. PMID 28498854 DOI: 10.1371/Journal.Pgen.1006728 |
0.42 |
|
| 2017 |
He KY, Wang H, Cade BE, Nandakumar P, Giri A, Ware EB, Haessler J, Liang J, Smith JA, Franceschini N, Le TH, Kooperberg C, Edwards TL, Kardia SL, Lin X, ... Chakravarti A, et al. Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure. Plos Genetics. 13: e1006678. PMID 28346479 DOI: 10.1371/Journal.Pgen.1006678 |
0.394 |
|
| 2017 |
Gui H, Schriemer D, Cheng WW, Chauhan RK, Antiňolo G, Berrios C, Bleda M, Brooks AS, Brouwer RW, Burns AJ, Cherny SS, Dopazo J, Eggen BJ, Griseri P, Jalloh B, ... ... Chakravarti A, et al. Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes. Genome Biology. 18: 48. PMID 28274275 DOI: 10.1186/S13059-017-1174-6 |
0.353 |
|
| 2017 |
Nandakumar P, Lee D, Richard MA, Tekola-Ayele F, Tayo BO, Ware E, Sung YJ, Salako B, Ogunniyi A, Gu CC, Grove ML, Fornage M, Kardia S, Rotima C, Cooper RS, ... ... Chakravarti A, et al. Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry. Journal of Hypertension. PMID 28234671 DOI: 10.1097/Hjh.0000000000001319 |
0.361 |
|
| 2017 |
Warren HR, Evangelou E, Cabrera CP, Gao H, Ren M, Mifsud B, Ntalla I, Surendran P, Liu C, Cook JP, Kraja AT, Drenos F, Loh M, Verweij N, Marten J, ... ... Chakravarti A, et al. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nature Genetics. PMID 28135244 DOI: 10.1038/Ng.3768 |
0.35 |
|
| 2016 |
Yoneyama S, Yao J, Guo X, Fernandez-Rhodes L, Lim U, Boston J, Buzková P, Carlson CS, Cheng I, Cochran B, Cooper R, Ehret G, Fornage M, Gong J, Gross M, ... ... Chakravarti A, et al. Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations. International Journal of Obesity (2005). PMID 27867202 DOI: 10.1038/Ijo.2016.207 |
0.362 |
|
| 2016 |
Hoffmann TJ, Ehret GB, Nandakumar P, Ranatunga D, Schaefer C, Kwok PY, Iribarren C, Chakravarti A, Risch N. Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Nature Genetics. PMID 27841878 DOI: 10.1038/Ng.3715 |
0.358 |
|
| 2016 |
Franceschini N, Carty CL, Lu Y, Tao R, Sung YJ, Manichaikul A, Haessler J, Fornage M, Schwander K, Zubair N, Bien S, Hindorff LA, Guo X, Bielinski SJ, Ehret G, ... ... Chakravarti A, et al. Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans. Plos One. 11: e0164132. PMID 27736895 DOI: 10.1371/Journal.Pone.0164132 |
0.372 |
|
| 2016 |
Tang CS, Gui H, Kapoor A, Kim JH, Luzón-Toro B, Pelet A, Burzynski G, Lantieri F, So MT, Berrios C, Shin HD, Fernández RM, Le TL, Verheij JB, Matera I, ... ... Chakravarti A, et al. Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. Human Molecular Genetics. PMID 27702942 DOI: 10.1093/Hmg/Ddw333 |
0.431 |
|
| 2016 |
Ehret GB, Ferreira T, Chasman DI, Jackson AU, Schmidt EM, Johnson T, Thorleifsson G, Luan J, Donnelly LA, Kanoni S, Petersen AK, Pihur V, Strawbridge RJ, Shungin D, Hughes MF, ... ... Chakravarti A, et al. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nature Genetics. PMID 27618452 DOI: 10.1038/Ng.3667 |
0.343 |
|
| 2016 |
Chakravarti A. Commentary: The central questions of human genetics: Richard Lewontin's 1968 senior lecture in Victor McKusick's Bar Harbor short course. International Journal of Epidemiology. 45: 668-72. PMID 27582441 DOI: 10.1093/Ije/Dyw184 |
0.302 |
|
| 2016 |
Chakravarti A, Turner TN. Revealing rate-limiting steps in complex disease biology: The crucial importance of studying rare, extreme-phenotype families. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. PMID 27062178 DOI: 10.1002/Bies.201500203 |
0.381 |
|
| 2016 |
Rose AM, Shah AZ, Venturini G, Krishna A, Chakravarti A, Rivolta C, Bhattacharya SS. Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosa. Scientific Reports. 6: 19450. PMID 26781568 DOI: 10.1038/Srep19450 |
0.379 |
|
| 2015 |
Yu B, Pulit SL, Hwang SJ, Brody JA, Amin N, Auer PL, Bis JC, Boerwinkle E, Burke GL, Chakravarti A, Correa A, Dreisbach AW, Franco OH, Ehret GB, Franceschini N, et al. Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk. Circulation. Cardiovascular Genetics. PMID 26658788 DOI: 10.1161/Circgenetics.115.001215 |
0.32 |
|
| 2015 |
Winkler TW, Justice AE, Graff M, Barata L, Feitosa MF, Chu S, Czajkowski J, Esko T, Fall T, Kilpeläinen TO, Lu Y, Mägi R, Mihailov E, Pers TH, Rüeger S, ... ... Chakravarti A, et al. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Plos Genetics. 11: e1005378. PMID 26426971 DOI: 10.1371/Journal.Pgen.1005378 |
0.327 |
|
| 2015 |
Chakravarti A. Perspectives on Human Variation through the Lens of Diversity and Race. Cold Spring Harbor Perspectives in Biology. 7: a023358. PMID 26330522 DOI: 10.1101/Cshperspect.A023358 |
0.394 |
|
| 2015 |
Cornish TC, Chakravarti A, Kapoor A, Halushka MK. HPASubC: A suite of tools for user subclassification of human protein atlas tissue images. Journal of Pathology Informatics. 6: 36. PMID 26167380 DOI: 10.4103/2153-3539.159213 |
0.499 |
|
| 2015 |
Chong JX, Buckingham KJ, Jhangiani SN, Boehm C, Sobreira N, Smith JD, Harrell TM, McMillin MJ, Wiszniewski W, Gambin T, Coban Akdemir ZH, Doheny K, Scott AF, Avramopoulos D, Chakravarti A, et al. The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities. American Journal of Human Genetics. 97: 199-215. PMID 26166479 DOI: 10.1016/J.Ajhg.2015.06.009 |
0.737 |
|
| 2015 |
Salfati E, Morrison AC, Boerwinkle E, Chakravarti A. Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC). Plos One. 10: e0133031. PMID 26162070 DOI: 10.1371/Journal.Pone.0133031 |
0.449 |
|
| 2015 |
Joshi PK, Esko T, Mattsson H, Eklund N, Gandin I, Nutile T, Jackson AU, Schurmann C, Smith AV, Zhang W, Okada Y, Stančáková A, Faul JD, Zhao W, Bartz TM, ... ... Chakravarti A, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 523: 459-62. PMID 26131930 DOI: 10.1038/Nature14618 |
0.393 |
|
| 2015 |
Manolio TA, Abramowicz M, Al-Mulla F, Anderson W, Balling R, Berger AC, Bleyl S, Chakravarti A, Chantratita W, Chisholm RL, W Dissanayake VH, Dunn M, Dzau VJ, Han BG, Hubbard T, et al. Global implementation of genomic medicine: We are not alone. Science Translational Medicine. 7: 290ps13. PMID 26041702 DOI: 10.1126/Scitranslmed.Aab0194 |
0.312 |
|
| 2015 |
Jiang Q, Arnold S, Heanue T, Kilambi KP, Doan B, Kapoor A, Ling AY, Sosa MX, Guy M, Jiang Q, Burzynski G, West K, Bessling S, Griseri P, Amiel J, ... ... Chakravarti A, et al. Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability. American Journal of Human Genetics. 96: 581-96. PMID 25839327 DOI: 10.1016/J.Ajhg.2015.02.014 |
0.36 |
|
| 2015 |
Turner TN, Sharma K, Oh EC, Liu YP, Collins RL, Sosa MX, Auer DR, Brand H, Sanders SJ, Moreno-De-Luca D, Pihur V, Plona T, Pike K, Soppet DR, Smith MW, ... ... Chakravarti A, et al. Loss of δ-catenin function in severe autism. Nature. 520: 51-6. PMID 25807484 DOI: 10.1038/Nature14186 |
0.364 |
|
| 2015 |
Dávila-Román VG, Sung YJ, Basson J, Cheng N, Nguyen KH, Nandakumar P, Hunt SC, Arnett DK, Rao DC, Chakravarti A, Badii R, Alkowari MK, Girotto G, Gasparini P, Mezzavilla M, et al. 43rd European Mathematical Genetics Meeting (EMGM) 2015. April 16-17, 2015, Brest, France: Abstracts Human Heredity. 79: 28-52. PMID 25791167 DOI: 10.1159/000381109 |
0.333 |
|
| 2015 |
Sung YJ, Basson J, Cheng N, Nguyen KD, Nandakumar P, Hunt SC, Arnett DK, Dávila-Román VG, Rao DC, Chakravarti A. The role of rare variants in systolic blood pressure: analysis of ExomeChip data in HyperGEN African Americans. Human Heredity. 79: 20-7. PMID 25765051 DOI: 10.1159/000375373 |
0.439 |
|
| 2015 |
Shungin D, Winkler TW, Croteau-Chonka DC, Ferreira T, Locke AE, Mägi R, Strawbridge RJ, Pers TH, Fischer K, Justice AE, Workalemahu T, Wu JM, Buchkovich ML, Heard-Costa NL, Roman TS, ... ... Chakravarti A, et al. New genetic loci link adipose and insulin biology to body fat distribution. Nature. 518: 187-96. PMID 25673412 DOI: 10.1038/Nature14132 |
0.331 |
|
| 2015 |
Chong JX, Buckingham KJ, Jhangiani SN, Boehm C, Sobreira N, Smith JD, Harrell TM, McMillin MJ, Wiszniewski W, Gambin T, CobanAkdemir ZH, Doheny K, Scott AF, Avramopoulos D, Chakravarti A, et al. The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities American Journal of Human Genetics. DOI: 10.1016/j.ajhg.2015.06.009 |
0.676 |
|
| 2014 |
Gunadi, Kapoor A, Ling AY, Rochadi, Makhmudi A, Herini ES, Sosa MX, Chatterjee S, Chakravarti A. Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease. Journal of Pediatric Surgery. 49: 1614-8. PMID 25475805 DOI: 10.1016/J.Jpedsurg.2014.04.011 |
0.336 |
|
| 2014 |
Chakravarti A. Profile of Mary-Claire King, 2014 Lasker-Koshland Special Achievement in Medical Science awardee. Proceedings of the National Academy of Sciences of the United States of America. 111: 17690-2. PMID 25425662 DOI: 10.1073/Pnas.1418785111 |
0.326 |
|
| 2014 |
Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K, Luan J, Kutalik Z, Amin N, Buchkovich ML, Croteau-Chonka DC, Day FR, Duan Y, ... ... Chakravarti A, et al. Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics. 46: 1173-86. PMID 25282103 DOI: 10.1038/Ng.3097 |
0.421 |
|
| 2014 |
Morrison AC, Bis JC, Hwang SJ, Ehret GB, Lumley T, Rice K, Muzny D, Gibbs RA, Boerwinkle E, Psaty BM, Chakravarti A, Levy D. Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study. Plos One. 9: e109155. PMID 25275628 DOI: 10.1371/Journal.Pone.0109155 |
0.418 |
|
| 2014 |
Hoggart CJ, Venturini G, Mangino M, Gomez F, Ascari G, Zhao JH, Teumer A, Winkler TW, TÅ¡ernikova N, Luan J, Mihailov E, Ehret GB, Zhang W, Lamparter D, Esko T, ... ... Chakravarti A, et al. Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index. Plos Genetics. 10: e1004508. PMID 25078964 DOI: 10.1371/Journal.Pgen.1004508 |
0.415 |
|
| 2014 |
Scharpf RB, Mireles L, Yang Q, Köttgen A, Ruczinski I, Susztak K, Halper-Stromberg E, Tin A, Cristiano S, Chakravarti A, Boerwinkle E, Fox CS, Coresh J, Linda Kao WH. Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrations. Bmc Genetics. 15: 81. PMID 25007794 DOI: 10.1186/1471-2156-15-81 |
0.377 |
|
| 2014 |
Ganesh SK, Chasman DI, Larson MG, Guo X, Verwoert G, Bis JC, Gu X, Smith AV, Yang ML, Zhang Y, Ehret G, Rose LM, Hwang SJ, Papanicolau GJ, Sijbrands EJ, ... ... Chakravarti A, et al. Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. American Journal of Human Genetics. 95: 49-65. PMID 24975945 DOI: 10.1016/J.Ajhg.2014.06.002 |
0.41 |
|
| 2014 |
Simino J, Shi G, Bis JC, Chasman DI, Ehret GB, Gu X, Guo X, Hwang SJ, Sijbrands E, Smith AV, Verwoert GC, Bragg-Gresham JL, Cadby G, Chen P, Cheng CY, ... ... Chakravarti A, et al. Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. American Journal of Human Genetics. 95: 24-38. PMID 24954895 DOI: 10.1016/J.Ajhg.2014.05.010 |
0.369 |
|
| 2014 |
Kapoor A, Sekar RB, Hansen NF, Fox-Talbot K, Morley M, Pihur V, Chatterjee S, Brandimarto J, Moravec CS, Pulit SL, Pfeufer A, Mullikin J, Ross M, Green ED, ... ... Chakravarti A, et al. An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval. American Journal of Human Genetics. 94: 854-69. PMID 24857694 DOI: 10.1016/J.Ajhg.2014.05.001 |
0.602 |
|
| 2014 |
Tragante V, Barnes MR, Ganesh SK, Lanktree MB, Guo W, Franceschini N, Smith EN, Johnson T, Holmes MV, Padmanabhan S, Karczewski KJ, Almoguera B, Barnard J, Baumert J, Chang YP, ... ... Chakravarti A, et al. Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. American Journal of Human Genetics. 94: 349-60. PMID 24560520 DOI: 10.1016/J.Ajhg.2013.12.016 |
0.411 |
|
| 2014 |
Lemaitre RN, Johnson CO, Hesselson S, Sotoodehnia N, Sotoodhenia N, McKnight B, Sitlani CM, Rea TD, King IB, Kwok PY, Mak A, Li G, Brody J, Larson E, Mozaffarian D, ... ... Chakravarti A, et al. Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 471-7. PMID 24418166 DOI: 10.1016/J.Hrthm.2014.01.008 |
0.307 |
|
| 2014 |
Matteini AM, Li J, Lange EM, Tanaka T, Lange LA, Tracy RP, Wang Y, Biggs ML, Arking DE, Fallin MD, Chakravarti A, Psaty BM, Bandinelli S, Ferrucci L, Reiner AP, et al. Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults. Cytokine. 65: 10-6. PMID 24182552 DOI: 10.1016/J.Cyto.2013.10.002 |
0.316 |
|
| 2013 |
Ganesh SK, Arnett DK, Assimes TL, Assimes TL, Basson CT, Chakravarti A, Ellinor PT, Engler MB, Goldmuntz E, Herrington DM, Hershberger RE, Hong Y, Johnson JA, Kittner SJ, McDermott DA, et al. Genetics and genomics for the prevention and treatment of cardiovascular disease: update: a scientific statement from the American Heart Association. Circulation. 128: 2813-51. PMID 24297835 DOI: 10.1161/01.Cir.0000437913.98912.1D |
0.43 |
|
| 2013 |
Fernández RM, Bleda M, Luzón-Toro B, García-Alonso L, Arnold S, Sribudiani Y, Besmond C, Lantieri F, Doan B, Ceccherini I, Lyonnet S, Hofstra RM, Chakravarti A, Antiñolo G, Dopazo J, et al. Pathways systematically associated to Hirschsprung's disease. Orphanet Journal of Rare Diseases. 8: 187. PMID 24289864 DOI: 10.1186/1750-1172-8-187 |
0.345 |
|
| 2013 |
Sampath S, Bhat S, Gupta S, O'Connor A, West AB, Arking DE, Chakravarti A. Defining the contribution of CNTNAP2 to autism susceptibility. Plos One. 8: e77906. PMID 24147096 DOI: 10.1371/Journal.Pone.0077906 |
0.371 |
|
| 2013 |
Prasad MK, Bhalla K, Pan ZH, O'Connell JR, Weder AB, Chakravarti A, Tian B, Chang YP. A polymorphic 3'UTR element in ATP1B1 regulates alternative polyadenylation and is associated with blood pressure. Plos One. 8: e76290. PMID 24098465 DOI: 10.1371/Journal.Pone.0076290 |
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| 2013 |
Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, Demirkan A, ... ... Chakravarti A, et al. Discovery and refinement of loci associated with lipid levels. Nature Genetics. 45: 1274-83. PMID 24097068 DOI: 10.1038/Ng.2797 |
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| 2013 |
Chakravarti A, Clark AG, Mootha VK. Distilling pathophysiology from complex disease genetics. Cell. 155: 21-6. PMID 24074858 DOI: 10.1016/J.Cell.2013.09.001 |
0.392 |
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| 2013 |
Franceschini N, Fox E, Zhang Z, Edwards TL, Nalls MA, Sung YJ, Tayo BO, Sun YV, Gottesman O, Adeyemo A, Johnson AD, Young JH, Rice K, Duan Q, Chen F, ... ... Chakravarti A, et al. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. American Journal of Human Genetics. 93: 545-54. PMID 23972371 DOI: 10.1016/J.Ajhg.2013.07.010 |
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| 2013 |
Jannot AS, Pelet A, Henrion-Caude A, Chaoui A, Masse-Morel M, Arnold S, Sanlaville D, Ceccherini I, Borrego S, Hofstra RM, Munnich A, Bondurand N, Chakravarti A, Clerget-Darpoux F, Amiel J, et al. Chromosome 21 scan in Down syndrome reveals DSCAM as a predisposing locus in Hirschsprung disease. Plos One. 8: e62519. PMID 23671607 DOI: 10.1371/Journal.Pone.0062519 |
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| 2013 |
Wu Y, Waite LL, Jackson AU, Sheu WH, Buyske S, Absher D, Arnett DK, Boerwinkle E, Bonnycastle LL, Carty CL, Cheng I, Cochran B, Croteau-Chonka DC, Dumitrescu L, Eaton CB, ... ... Chakravarti A, et al. Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. Plos Genetics. 9: e1003379. PMID 23555291 DOI: 10.1371/Journal.Pgen.1003379 |
0.39 |
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| 2013 |
Shah SA, Herrington DM, Howard TD, Divers J, Arnett DK, Burke GL, Kao WH, Guo X, Siscovick DS, Chakravarti A, Lima JA, Psaty BM, Tomaselli GF, Rich SS, Bowden DW, et al. Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA). Annals of Noninvasive Electrocardiology : the Official Journal of the International Society For Holter and Noninvasive Electrocardiology, Inc. 18: 29-40. PMID 23347024 DOI: 10.1111/Anec.12028 |
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| 2013 |
Crosslin DR, McDavid A, Weston N, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Ritchie MD, Saip A, Crawford DC, ... ... Chakravarti A, et al. Genetic variation associated with circulating monocyte count in the eMERGE Network. Human Molecular Genetics. 22: 2119-27. PMID 23314186 DOI: 10.1093/Hmg/Ddt010 |
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| 2013 |
Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YP, Elbers CC, Farrall M, Fischer ME, Franceschini N, ... ... Chakravarti A, et al. Loci influencing blood pressure identified using a cardiovascular gene-centric array. Human Molecular Genetics. 22: 1663-78. PMID 23303523 DOI: 10.1093/Hmg/Dds555 |
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| 2013 |
Nguyen KD, Pihur V, Ganesh SK, Rakha A, Cooper RS, Hunt SC, Freedman BI, Coresh J, Kao WH, Morrison AC, Boerwinkle E, Ehret GB, Chakravarti A. Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies. Circulation Research. 112: 318-26. PMID 23149595 DOI: 10.1161/Circresaha.112.276725 |
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| 2013 |
Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YPC, Elbers CC, Farrall M, Fischer ME, Gaunt NF, ... ... Chakravarti A, et al. Loci influencing blood pressure identified using a cardiovascular gene-centric array Human Molecular Genetics. 22: 3394-3395. DOI: 10.1093/Hmg/Ddt177 |
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| 2012 |
Sosa MX, Sivakumar IK, Maragh S, Veeramachaneni V, Hariharan R, Parulekar M, Fredrikson KM, Harkins TT, Lin J, Feldman AB, Tata P, Ehret GB, Chakravarti A. Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency. Plos Computational Biology. 8: e1002737. PMID 23133345 DOI: 10.1371/Journal.Pcbi.1002737 |
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| 2012 |
Ellinor PT, Lunetta KL, Albert CM, Glazer NL, Ritchie MD, Smith AV, Arking DE, Müller-Nurasyid M, Krijthe BP, Lubitz SA, Bis JC, Chung MK, Dörr M, Ozaki K, Roberts JD, ... ... Chakravarti A, et al. Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nature Genetics. 44: 670-5. PMID 22544366 DOI: 10.1038/Ng.2261 |
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| 2012 |
Chakravarti A. 2011 introduction to Curt Stern Award. American Journal of Human Genetics. 90: 405-6. PMID 22405085 DOI: 10.1016/J.Ajhg.2012.02.015 |
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| 2012 |
Jiang Q, Turner T, Sosa MX, Rakha A, Arnold S, Chakravarti A. Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer. Human Mutation. 33: 281-9. PMID 21898659 DOI: 10.1002/Humu.21602 |
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| 2012 |
Amin N, Byrne E, Johnson J, Chenevix-Trench G, Walter S, Nolte IM, Vink JM, Rawal R, Mangino M, Teumer A, Keers JC, Verwoert G, Baumeister S, Biffar R, ... ... Chakravarti A, et al. Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Molecular Psychiatry. 17: 1116-29. PMID 21876539 DOI: 10.1038/Mp.2011.101 |
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| 2012 |
Chakravarti A, Kapoor A. Genetics and genomics in cardiovascular gene discovery Muscle. 1: 231-259. DOI: 10.1016/B978-0-12-381510-1.00018-1 |
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| 2011 |
Won JH, Ehret G, Chakravarti A, Olshen RA. SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension. Plos One. 6: e27891. PMID 22140480 DOI: 10.1371/Journal.Pone.0027891 |
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| 2011 |
Chakravarti A. Widespread promiscuous genetic information transfer from DNA to RNA. Circulation Research. 109: 1202-3. PMID 22076505 DOI: 10.1161/Res.0B013E31823C4992 |
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| 2011 |
Turner T, Pihur V, Chakravarti A. Quantifying and modeling birth order effects in autism. Plos One. 6: e26418. PMID 22039484 DOI: 10.1371/Journal.Pone.0026418 |
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| 2011 |
Chakravarti A. Genomics is not enough. Science (New York, N.Y.). 334: 15. PMID 21980079 DOI: 10.1126/Science.1214458 |
0.423 |
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| 2011 |
Benke KS, Carlson MC, Doan BQ, Walston JD, Xue QL, Reiner AP, Fried LP, Arking DE, Chakravarti A, Fallin MD. The association of genetic variants in interleukin-1 genes with cognition: findings from the cardiovascular health study. Experimental Gerontology. 46: 1010-9. PMID 21968104 DOI: 10.1016/J.Exger.2011.09.005 |
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| 2011 |
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, ... ... Chakravarti A, et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 478: 103-9. PMID 21909115 DOI: 10.1038/Nature10405 |
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| 2011 |
Ho YY, Matteini AM, Beamer B, Fried L, Xue QL, Arking DE, Chakravarti A, Fallin MD, Walston J. Exploring biologically relevant pathways in frailty. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 66: 975-9. PMID 21743092 DOI: 10.1093/Gerona/Glr061 |
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| 2011 |
Arking DE, Junttila MJ, Goyette P, Huertas-Vazquez A, Eijgelsheim M, Blom MT, Newton-Cheh C, Reinier K, Teodorescu C, Uy-Evanado A, Carter-Monroe N, Kaikkonen KS, Kortelainen ML, Boucher G, Lagacé C, ... ... Chakravarti A, et al. Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. Plos Genetics. 7: e1002158. PMID 21738491 DOI: 10.1371/Journal.Pgen.1002158 |
0.387 |
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| 2011 |
Nalls MA, Couper DJ, Tanaka T, van Rooij FJ, Chen MH, Smith AV, Toniolo D, Zakai NA, Yang Q, Greinacher A, Wood AR, Garcia M, Gasparini P, Liu Y, Lumley T, ... ... Chakravarti A, et al. Multiple loci are associated with white blood cell phenotypes. Plos Genetics. 7: e1002113. PMID 21738480 DOI: 10.1371/Journal.Pgen.1002113 |
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| 2011 |
Jiang Q, Ho YY, Hao L, Nichols Berrios C, Chakravarti A. Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease. Plos One. 6: e21219. PMID 21712996 DOI: 10.1371/Journal.Pone.0021219 |
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| 2011 |
Burns KH, Chakravarti A. Massively parallel rare disease genetics. Genome Medicine. 3: 29. PMID 21635711 DOI: 10.1186/Gm244 |
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| 2011 |
Chakravarti A. Genomic contributions to Mendelian disease. Genome Research. 21: 643-4. PMID 21536725 DOI: 10.1101/Gr.123554.111 |
0.369 |
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| 2011 |
Johnson AD, Newton-Cheh C, Chasman DI, Ehret GB, Johnson T, Rose L, Rice K, Verwoert GC, Launer LJ, Gudnason V, Larson MG, Chakravarti A, Psaty BM, Caulfield M, van Duijn CM, et al. Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals. Hypertension. 57: 903-10. PMID 21444836 DOI: 10.1161/Hypertensionaha.110.158667 |
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| 2011 |
Zhu X, Young JH, Fox E, Keating BJ, Franceschini N, Kang S, Tayo B, Adeyemo A, Sun YV, Li Y, Morrison A, Newton-Cheh C, Liu K, Ganesh SK, Kutlar A, ... ... Chakravarti A, et al. Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium. Human Molecular Genetics. 20: 2285-95. PMID 21422096 DOI: 10.1093/Hmg/Ddr113 |
0.468 |
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| 2011 |
Fox ER, Young JH, Li Y, Dreisbach AW, Keating BJ, Musani SK, Liu K, Morrison AC, Ganesh S, Kutlar A, Ramachandran VS, Polak JF, Fabsitz RR, Dries DL, Farlow DN, ... ... Chakravarti A, et al. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Human Molecular Genetics. 20: 2273-84. PMID 21378095 DOI: 10.1093/Hmg/Ddr092 |
0.427 |
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| 2011 |
Lettre G, Palmer CD, Young T, Ejebe KG, Allayee H, Benjamin EJ, Bennett F, Bowden DW, Chakravarti A, Dreisbach A, Farlow DN, Folsom AR, Fornage M, Forrester T, Fox E, et al. Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. Plos Genetics. 7: e1001300. PMID 21347282 DOI: 10.1371/Journal.Pgen.1001300 |
0.402 |
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| 2011 |
Shi G, Boerwinkle E, Morrison AC, Gu CC, Chakravarti A, Rao DC. Mining gold dust under the genome wide significance level: a two-stage approach to analysis of GWAS. Genetic Epidemiology. 35: 111-8. PMID 21254218 DOI: 10.1002/Gepi.20556 |
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| 2011 |
Simino J, Shi G, Kume R, Schwander K, Province MA, Gu CC, Kardia S, Chakravarti A, Ehret G, Olshen RA, Turner ST, Ho LT, Zhu X, Jaquish C, Paltoo D, et al. Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program. American Journal of Hypertension. 24: 347-54. PMID 21151011 DOI: 10.1038/Ajh.2010.238 |
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| 2011 |
Scharpf RB, Ruczinski I, Carvalho B, Doan B, Chakravarti A, Irizarry RA. A multilevel model to address batch effects in copy number estimation using SNP arrays. Biostatistics (Oxford, England). 12: 33-50. PMID 20625178 DOI: 10.1093/Biostatistics/Kxq043 |
0.376 |
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| 2010 |
Sotoodehnia N, Isaacs A, de Bakker PI, Dörr M, Newton-Cheh C, Nolte IM, van der Harst P, Müller M, Eijgelsheim M, Alonso A, Hicks AA, Padmanabhan S, Hayward C, Smith AV, Polasek O, ... ... Chakravarti A, et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nature Genetics. 42: 1068-76. PMID 21076409 DOI: 10.1038/Ng.716 |
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| 2010 |
Fradin D, Cheslack-Postava K, Ladd-Acosta C, Newschaffer C, Chakravarti A, Arking DE, Feinberg A, Fallin MD. Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs. Plos One. 5. PMID 20824079 DOI: 10.1371/Journal.Pone.0012513 |
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| 2010 |
Meyer TE, Verwoert GC, Hwang SJ, Glazer NL, Smith AV, van Rooij FJ, Ehret GB, Boerwinkle E, Felix JF, Leak TS, Harris TB, Yang Q, Dehghan A, Aspelund T, Katz R, ... ... Chakravarti A, et al. Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels. Plos Genetics. 6. PMID 20700443 DOI: 10.1371/Journal.Pgen.1001045 |
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| 2010 |
Emison ES, Garcia-Barcelo M, Grice EA, Lantieri F, Amiel J, Burzynski G, Fernandez RM, Hao L, Kashuk C, West K, Miao X, Tam PK, Griseri P, Ceccherini I, Pelet A, ... ... Chakravarti A, et al. Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability. American Journal of Human Genetics. 87: 60-74. PMID 20598273 DOI: 10.1016/J.Ajhg.2010.06.007 |
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| 2010 |
Tomás M, Napolitano C, De Giuli L, Bloise R, Subirana I, Malovini A, Bellazzi R, Arking DE, Marban E, Chakravarti A, Spooner PM, Priori SG. Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome. Journal of the American College of Cardiology. 55: 2745-52. PMID 20538168 DOI: 10.1016/J.Jacc.2009.12.065 |
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| 2010 |
Antonarakis SE, Chakravarti A, Cohen JC, Hardy J. Mendelian disorders and multifactorial traits: the big divide or one for all? Nature Reviews. Genetics. 11: 380-4. PMID 20395971 DOI: 10.1038/Nrg2793 |
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| 2010 |
Arking DE, Reinier K, Post W, Jui J, Hilton G, O'Connor A, Prineas RJ, Boerwinkle E, Psaty BM, Tomaselli GF, Rea T, Sotoodehnia N, Siscovick DS, Burke GL, Marban E, ... ... Chakravarti A, et al. Genome-wide association study identifies GPC5 as a novel genetic locus protective against sudden cardiac arrest. Plos One. 5: e9879. PMID 20360844 DOI: 10.1371/Journal.Pone.0009879 |
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| 2010 |
Ellinor PT, Lunetta KL, Glazer NL, Pfeufer A, Alonso A, Chung MK, Sinner MF, de Bakker PI, Mueller M, Lubitz SA, Fox E, Darbar D, Smith NL, Smith JD, Schnabel RB, ... ... Chakravarti A, et al. Common variants in KCNN3 are associated with lone atrial fibrillation. Nature Genetics. 42: 240-4. PMID 20173747 DOI: 10.1038/Ng.537 |
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| 2010 |
Pfeufer A, van Noord C, Marciante KD, Arking DE, Larson MG, Smith AV, Tarasov KV, Müller M, Sotoodehnia N, Sinner MF, Verwoert GC, Li M, Kao WH, Köttgen A, Coresh J, ... ... Chakravarti A, et al. Genome-wide association study of PR interval. Nature Genetics. 42: 153-9. PMID 20062060 DOI: 10.1038/Ng.517 |
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| 2010 |
North KE, Franceschini N, Avery CL, Baird L, Graff M, Leppert M, Chung JH, Zhang J, Hanis C, Boerwinkle E, Volcik KA, Grove ML, Mosley TH, Gu C, Heiss G, ... ... Chakravarti A, et al. Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations. Acta Diabetologica. 47: 199-207. PMID 19855918 DOI: 10.1007/S00592-009-0162-Z |
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| 2009 |
Ganesh SK, Zakai NA, van Rooij FJ, Soranzo N, Smith AV, Nalls MA, Chen MH, Kottgen A, Glazer NL, Dehghan A, Kuhnel B, Aspelund T, Yang Q, Tanaka T, Jaffe A, ... ... Chakravarti A, et al. Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Nature Genetics. 41: 1191-8. PMID 19862010 DOI: 10.1038/Ng.466 |
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| 2009 |
Weiss LA, Arking DE, Daly MJ, Chakravarti A, Brune CW, West K, O'Connor A, Hilton G, Tomlinson RL, West AB, Cook EH, Green T, Chang SC, Gabriel S, Gates C, et al. A genome-wide linkage and association scan reveals novel loci for autism Nature. 461: 802-808. PMID 19812673 DOI: 10.1038/Nature08490 |
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| 2009 |
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, Cho JH, Guttmacher AE, Kong A, Kruglyak L, Mardis E, et al. Finding the missing heritability of complex diseases. Nature. 461: 747-53. PMID 19812666 DOI: 10.1038/Nature08494 |
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| 2009 |
Chakravarti A. Human genetics: Tracing India's invisible threads. Nature. 461: 487-8. PMID 19779444 DOI: 10.1038/461487A |
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| 2009 |
Arking DE, Chakravarti A. Understanding cardiovascular disease through the lens of genome-wide association studies. Trends in Genetics : Tig. 25: 387-94. PMID 19716196 DOI: 10.1016/J.Tig.2009.07.007 |
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| 2009 |
Milan DJ, Kim AM, Winterfield JR, Jones IL, Pfeufer A, Sanna S, Arking DE, Amsterdam AH, Sabeh KM, Mably JD, Rosenbaum DS, Peterson RT, Chakravarti A, Kääb S, Roden DM, et al. Drug-sensitized zebrafish screen identifies multiple genes, including GINS3, as regulators of myocardial repolarization. Circulation. 120: 553-9. PMID 19652097 DOI: 10.1161/Circulationaha.108.821082 |
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| 2009 |
Ehret GB, O'Connor AA, Weder A, Cooper RS, Chakravarti A. Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study. European Journal of Human Genetics : Ejhg. 17: 1650-7. PMID 19536175 DOI: 10.1038/Ejhg.2009.94 |
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| 2009 |
Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, Glazer NL, Morrison AC, Johnson AD, Aspelund T, Aulchenko Y, Lumley T, Köttgen A, Vasan RS, Rivadeneira F, ... ... Chakravarti A, et al. Genome-wide association study of blood pressure and hypertension. Nature Genetics. 41: 677-87. PMID 19430479 DOI: 10.1038/Ng.384 |
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| 2009 |
Joe B, Saad Y, Dhindaw S, Lee NH, Frank BC, Achinike OH, Luu TV, Gopalakrishnan K, Toland EJ, Farms P, Yerga-Woolwine S, Manickavasagam E, Rapp JP, Garrett MR, Coe D, ... ... Chakravarti A, et al. Positional identification of variants of Adamts16 linked to inherited hypertension. Human Molecular Genetics. 18: 2825-38. PMID 19423552 DOI: 10.1093/Hmg/Ddp218 |
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| 2009 |
Arnold S, Pelet A, Amiel J, Borrego S, Hofstra R, Tam P, Ceccherini I, Lyonnet S, Sherman S, Chakravarti A. Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association. Human Mutation. 30: 771-5. PMID 19306335 DOI: 10.1002/Humu.20944 |
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| 2009 |
Pfeufer A, Sanna S, Arking DE, Müller M, Gateva V, Fuchsberger C, Ehret GB, Orrú M, Pattaro C, Köttgen A, Perz S, Usala G, Barbalic M, Li M, Pütz B, ... ... Chakravarti A, et al. Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nature Genetics. 41: 407-14. PMID 19305409 DOI: 10.1038/Ng.362 |
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| 2009 |
Dezentje DA, Arking DE, Kortenhorst MS, West K, Chakravarti A, Kern SE. Hybrids of aneuploid human cancer cells permit complementation of simple and complex cancer defects. Cancer Biology & Therapy. 8: 347-55. PMID 19305140 DOI: 10.4161/Cbt.8.4.7346 |
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| 2009 |
Franceschini N, North KE, Arnett D, Pankow JS, Chung JH, Baird L, Leppert MF, Eckfeldt JH, Boerwinkle E, Gu CC, Lewis CE, Myers RH, Turner ST, Weder A, Kao WH, ... ... Chakravarti A, et al. 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. 22: 552-8. PMID 19265784 DOI: 10.1038/Ajh.2009.41 |
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| 2009 |
Kao WH, Arking DE, Post W, Rea TD, Sotoodehnia N, Prineas RJ, Bishe B, Doan BQ, Boerwinkle E, Psaty BM, Tomaselli GF, Coresh J, Siscovick DS, Marbán E, Spooner PM, ... ... Chakravarti A, et al. Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations. Circulation. 119: 940-51. PMID 19204306 DOI: 10.1161/Circulationaha.108.791723 |
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| 2009 |
Arking DE, Khera A, Xing C, Kao WH, Post W, Boerwinkle E, Chakravarti A. Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population. Plos One. 4: e4333. PMID 19180230 DOI: 10.1371/Journal.Pone.0004333 |
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| 2009 |
Chakravarti A. Being human: kinship: race relations. Nature. 457: 380-1. PMID 19158772 DOI: 10.1038/457380A |
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| 2009 |
Wang Y, O'Connell JR, McArdle PF, Wade JB, Dorff SE, Shah SJ, Shi X, Pan L, Rampersaud E, Shen H, Kim JD, Subramanya AR, Steinle NI, Parsa A, Ober CC, ... ... Chakravarti A, et al. 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. 106: 226-31. PMID 19114657 DOI: 10.1073/Pnas.0808358106 |
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| 2008 |
Ehret GB, Morrison AC, O'Connor AA, Grove ML, Baird L, Schwander K, Weder A, Cooper RS, Rao DC, Hunt SC, Boerwinkle E, Chakravarti A. Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program. European Journal of Human Genetics : Ejhg. 16: 1507-11. PMID 18523456 DOI: 10.1038/Ejhg.2008.102 |
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| 2008 |
Lin S, Carvalho B, Cutler DJ, Arking DE, Chakravarti A, Irizarry RA. Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays. Genome Biology. 9: R63. PMID 18387188 DOI: 10.1186/Gb-2008-9-4-R63 |
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| 2008 |
Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, et al. Association between microdeletion and microduplication at 16p11.2 and autism. The New England Journal of Medicine. 358: 667-75. PMID 18184952 DOI: 10.1056/Nejmoa075974 |
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| 2008 |
Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics. 82: 160-4. PMID 18179894 DOI: 10.1016/J.Ajhg.2007.09.015 |
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| 2008 |
Tan AC, Fan JB, Karikari C, Bibikova M, Garcia EW, Zhou L, Barker D, Serre D, Feldmann G, Hruban RH, Klein AP, Goggins M, Couch FJ, Hudson TJ, Winslow RL, ... ... Chakravarti A, et al. Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discovery. Cancer Biology & Therapy. 7: 135-44. PMID 18059179 DOI: 10.4161/Cbt.7.1.5199 |
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| 2007 |
Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, Byrne EH, McCarroll SA, Gaudet R, Schaffner SF, Lander ES, Frazer KA, Ballinger DG, ... ... Chakravarti A, et al. Genome-wide detection and characterization of positive selection in human populations. Nature. 449: 913-8. PMID 17943131 DOI: 10.1038/Nature06250 |
0.608 |
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| 2007 |
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, ... ... Chakravarti A, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature. 449: 851-61. PMID 17943122 DOI: 10.1038/Nature06258 |
0.621 |
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| 2007 |
Gherman A, Chen PE, Teslovich TM, Stankiewicz P, Withers M, Kashuk CS, Chakravarti A, Lupski JR, Cutler DJ, Katsanis N. Population bottlenecks as a potential major shaping force of human genome architecture. Plos Genetics. 3: e119. PMID 17658953 DOI: 10.1371/Journal.Pgen.0030119 |
0.58 |
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| 2007 |
Scuteri A, Sanna S, Chen WM, Uda M, Albai G, Strait J, Najjar S, Nagaraja R, Orrú M, Usala G, Dei M, Lai S, Maschio A, Busonero F, Mulas A, ... ... Chakravarti A, et al. Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. Plos Genetics. 3: e115. PMID 17658951 DOI: 10.1371/Journal.Pgen.0030115 |
0.406 |
|
| 2007 |
Wen G, Wessel J, Zhou W, Ehret GB, Rao F, Stridsberg M, Mahata SK, Gent PM, Das M, Cooper RS, Chakravarti A, Zhou H, Schork NJ, O'connor DT, Hamilton BA. An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension. Human Molecular Genetics. 16: 1752-64. PMID 17584765 DOI: 10.1093/Hmg/Ddm123 |
0.39 |
|
| 2007 |
Post W, Shen H, Damcott C, Arking DE, Kao WHL, Sack PA, Ryan KA, Chakravarti A, Mitchell BD, Shuldiner AR. Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the Old Order Amish Human Heredity. 64: 214-219. PMID 17565224 DOI: 10.1159/000103630 |
0.403 |
|
| 2007 |
Gu CC, Hunt SC, Kardia S, Turner ST, Chakravarti A, Schork N, Olshen R, Curb D, Jaquish C, Boerwinkle E, Rao DC. An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP). Human Genetics. 121: 577-90. PMID 17372766 DOI: 10.1007/S00439-007-0349-8 |
0.399 |
|
| 2007 |
Zlotogora J, Hujerat Y, Barges S, Shalev SA, Chakravarti A. The fate of 12 recessive mutations in a single village. Annals of Human Genetics. 71: 202-8. PMID 17331080 DOI: 10.1111/J.1469-1809.2006.00308.X |
0.305 |
|
| 2007 |
Chang YP, Liu X, Kim JD, Ikeda MA, Layton MR, Weder AB, Cooper RS, Kardia SL, Rao DC, Hunt SC, Luke A, Boerwinkle E, Chakravarti A. Multiple genes for essential-hypertension susceptibility on chromosome 1q. American Journal of Human Genetics. 80: 253-64. PMID 17236131 DOI: 10.1086/510918 |
0.449 |
|
| 2006 |
Blackman SM, Deering-Brose R, McWilliams R, Naughton K, Coleman B, Lai T, Algire M, Beck S, Hoover-Fong J, Hamosh A, Fallin MD, West K, Arking DE, Chakravarti A, Cutler DJ, et al. Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis. Gastroenterology. 131: 1030-9. PMID 17030173 DOI: 10.1053/J.Gastro.2006.07.016 |
0.521 |
|
| 2006 |
Calhoun ES, Hucl T, Gallmeier E, West KM, Arking DE, Maitra A, Iacobuzio-Donahue CA, Chakravarti A, Hruban RH, Kern SE. Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays. Cancer Research. 66: 7920-8. PMID 16912165 DOI: 10.1158/0008-5472.Can-06-0721 |
0.407 |
|
| 2006 |
Arking DE, Fallin DM, Fried LP, Li T, Beamer BA, Xue QL, Chakravarti A, Walston J. Variation in the ciliary neurotrophic factor gene and muscle strength in older Caucasian women. Journal of the American Geriatrics Society. 54: 823-6. PMID 16696750 DOI: 10.1111/J.1532-5415.2006.00693.X |
0.379 |
|
| 2006 |
Arking DE, Pfeufer A, Post W, Kao WH, Newton-Cheh C, Ikeda M, West K, Kashuk C, Akyol M, Perz S, Jalilzadeh S, Illig T, Gieger C, Guo CY, Larson MG, ... ... Chakravarti A, et al. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nature Genetics. 38: 644-51. PMID 16648850 DOI: 10.1038/Ng1790 |
0.388 |
|
| 2006 |
Zlotogora J, Carasquillo M, Barges S, Shalev SA, Hujerat Y, Chakravarti A. High incidence of deafness from three frequent connexin 26 mutations in an isolated community. Genetic Testing. 10: 40-3. PMID 16545002 DOI: 10.1089/Gte.2006.10.40 |
0.302 |
|
| 2006 |
Laramie JM, Wilk JB, Hunt SC, Ellison RC, Chakravarti A, Boerwinkle E, Myers RH. 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. 7: 17. PMID 16509988 DOI: 10.1186/1471-2350-7-17 |
0.34 |
|
| 2006 |
Chang YP, Kim JD, Schwander K, Rao DC, Miller MB, Weder AB, Cooper RS, Schork NJ, Province MA, Morrison AC, Kardia SL, Quertermous T, Chakravarti A. 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. 14: 469-77. PMID 16493446 DOI: 10.1038/Sj.Ejhg.5201582 |
0.39 |
|
| 2005 |
Young JH, Chang YP, Kim JD, Chretien JP, Klag MJ, Levine MA, Ruff CB, Wang NY, Chakravarti A. Differential susceptibility to hypertension is due to selection during the out-of-Africa expansion. Plos Genetics. 1: e82. PMID 16429165 DOI: 10.1371/Journal.Pgen.0010082 |
0.349 |
|
| 2005 |
Gu CC, Chang YP, Hunt SC, Schwander K, Arnett D, Djousse L, Heiss G, Oberman A, Lalouel JM, Province M, Chakravarti A, Rao DC. Haplotype association analysis of AGT variants with hypertension-related traits: the HyperGEN study. Human Heredity. 60: 164-76. PMID 16352906 DOI: 10.1159/000090118 |
0.37 |
|
| 2005 |
Rasmussen-Torvik LJ, North KE, Gu CC, Lewis CE, Wilk JB, Chakravarti A, Chang YP, Miller MB, Li N, Devereux RB, Arnett DK. A population association study of angiotensinogen polymorphisms and haplotypes with left ventricular phenotypes. Hypertension. 46: 1294-9. PMID 16286570 DOI: 10.1161/01.Hyp.0000192653.17209.84 |
0.397 |
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| 2005 |
Grice EA, Rochelle ES, Green ED, Chakravarti A, McCallion AS. Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer. Human Molecular Genetics. 14: 3837-45. PMID 16269442 DOI: 10.1093/Hmg/Ddi408 |
0.307 |
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| 2005 |
Armanios M, Chen JL, Chang YP, Brodsky RA, Hawkins A, Griffin CA, Eshleman JR, Cohen AR, Chakravarti A, Hamosh A, Greider CW. 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. 102: 15960-4. PMID 16247010 DOI: 10.1073/Pnas.0508124102 |
0.303 |
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| 2005 |
Maitra A, Arking DE, Shivapurkar N, Ikeda M, Stastny V, Kassauei K, Sui G, Cutler DJ, Liu Y, Brimble SN, Noaksson K, Hyllner J, Schulz TC, Zeng X, Freed WJ, ... ... Chakravarti A, et al. Genomic alterations in cultured human embryonic stem cells. Nature Genetics. 37: 1099-103. PMID 16142235 DOI: 10.1038/Ng1631 |
0.565 |
|
| 2005 |
Mitchell AA, Chakravarti A, Cutler DJ. On the probability that a novel variant is a disease-causing mutation. Genome Research. 15: 960-6. PMID 15965029 DOI: 10.1101/Gr.3761405 |
0.571 |
|
| 2005 |
Kashuk CS, Stone EA, Grice EA, Portnoy ME, Green ED, Sidow A, Chakravarti A, McCallion AS. 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. 102: 8949-54. PMID 15956201 DOI: 10.1073/Pnas.0503259102 |
0.359 |
|
| 2005 |
Emison ES, McCallion AS, Kashuk CS, Bush RT, Grice E, Lin S, Portnoy ME, Cutler DJ, Green ED, Chakravarti A. A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk. Nature. 434: 857-63. PMID 15829955 DOI: 10.1038/Nature03467 |
0.596 |
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| 2004 |
Lin S, Chakravarti A, Cutler DJ. Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies. Nature Genetics. 36: 1181-8. PMID 15502828 DOI: 10.1038/Ng1457 |
0.611 |
|
| 2004 |
Chakravarti A. Finding needles in haystacks--IRF6 gene variants in isolated cleft lip or cleft palate. The New England Journal of Medicine. 351: 822-4. PMID 15317897 DOI: 10.1056/Nejme048164 |
0.419 |
|
| 2004 |
Lin S, Chakravarti A, Cutler DJ. Haplotype and missing data inference in nuclear families. Genome Research. 14: 1624-32. PMID 15256514 DOI: 10.1101/Gr.2204604 |
0.586 |
|
| 2004 |
Arking DE, Chugh SS, Chakravarti A, Spooner PM. Genomics in sudden cardiac death. Circulation Research. 94: 712-23. PMID 15059941 DOI: 10.1161/01.Res.0000123861.16082.95 |
0.361 |
|
| 2004 |
Mitchell AA, Zwick ME, Chakravarti A, Cutler DJ. Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns. Bioinformatics (Oxford, England). 20: 1022-32. PMID 14764571 DOI: 10.1093/Bioinformatics/Bth034 |
0.766 |
|
| 2004 |
Xu Z, Kerstann KF, Sherman SL, Chakravarti A, Feingold E. A trisomic transmission disequilibrium test. Genetic Epidemiology. 26: 125-31. PMID 14748012 DOI: 10.1002/Gepi.10302 |
0.369 |
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| 2004 |
Barkley RA, Chakravarti A, Cooper RS, Ellison RC, Hunt SC, Province MA, Turner ST, Weder AB, Boerwinkle E. Positional identification of hypertension susceptibility genes on chromosome 2. Hypertension. 43: 477-82. PMID 14732741 DOI: 10.1161/01.Hyp.0000111585.76299.F7 |
0.423 |
|
| 2004 |
Chakravarti A. Ching Chun Li (1912–2003):A Personal Remembrance of a Hero of Genetics The American Journal of Human Genetics. 74: 789-792. DOI: 10.1086/420857 |
0.359 |
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| 2003 |
McCallion AS, Emison ES, Kashuk CS, Bush RT, Kenton M, Carrasquillo MM, Jones KW, Kennedy GC, Portnoy ME, Green ED, Chakravarti A. Genomic variation in multigenic traits: Hirschsprung disease. Cold Spring Harbor Symposia On Quantitative Biology. 68: 373-81. PMID 15338639 DOI: 10.1101/Sqb.2003.68.373 |
0.353 |
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| 2003 |
Thomas JW, Touchman JW, Blakesley RW, Bouffard GG, Beckstrom-Sternberg SM, Margulies EH, Blanchette M, Siepel AC, Thomas PJ, McDowell JC, Maskeri B, Hansen NF, Schwartz MS, Weber RJ, Kent WJ, ... ... Chakravarti A, et al. Comparative analyses of multi-species sequences from targeted genomic regions. Nature. 424: 788-93. PMID 12917688 DOI: 10.1038/Nature01858 |
0.572 |
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| 2003 |
Zhu X, Chang YP, Yan D, Weder A, Cooper R, Luke A, Kan D, Chakravarti A. Associations between hypertension and genes in the renin-angiotensin system. Hypertension (Dallas, Tex. : 1979). 41: 1027-34. PMID 12695419 DOI: 10.1161/01.Hyp.0000068681.69874.Cb |
0.39 |
|
| 2003 |
Weder AB, Delgado MC, Zhu X, Gleiberman L, Kan D, Chakravarti A. Erythrocyte sodium-lithium countertransport and blood pressure: A genome-wide linkage study Hypertension. 41: 842-846. PMID 12624006 DOI: 10.1161/01.Hyp.0000048703.16933.6D |
0.39 |
|
| 2003 |
Sen S, Nesse RM, Stoltenberg SF, Li S, Gleiberman L, Chakravarti A, Weder AB, Burmeister M. 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. 28: 397-401. PMID 12589394 DOI: 10.1038/Sj.Npp.1300053 |
0.35 |
|
| 2003 |
Mitchell AA, Cutler DJ, Chakravarti A. Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test. American Journal of Human Genetics. 72: 598-610. PMID 12587097 DOI: 10.1086/368203 |
0.6 |
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| 2003 |
McCallion AS, Stames E, Conlon RA, Chakravarti A. 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. 100: 1826-31. PMID 12574515 DOI: 10.1073/Pnas.0337540100 |
0.374 |
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| 2003 |
Zhu X, Yan D, Cooper RS, Luke A, Ikeda MA, Chang YP, Weder A, Chakravarti A. Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program. Genome Research. 13: 173-81. PMID 12566395 DOI: 10.1101/Gr.302003 |
0.427 |
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| 2003 |
Thiel BA, Chakravarti A, Cooper RS, Luke A, Lewis S, Lynn A, Tiwari H, Schork NJ, Weder AB. A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans. American Journal of Hypertension. 16: 151-3. PMID 12559684 DOI: 10.1016/S0895-7061(02)03246-6 |
0.385 |
|
| 2003 |
Marth G, Schuler G, Yeh R, Davenport R, Agarwala R, Church D, Wheelan S, Baker J, Ward M, Kholodov M, Phan L, Czabarka E, Murvai J, Cutler D, Wooding S, ... ... Chakravarti A, et al. 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. 100: 376-81. PMID 12502794 DOI: 10.1073/Pnas.222673099 |
0.606 |
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| 2002 |
Lin S, Cutler DJ, Zwick ME, Chakravarti A. Haplotype inference in random population samples. American Journal of Human Genetics. 71: 1129-37. PMID 12386835 DOI: 10.1086/344347 |
0.765 |
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| 2002 |
Merikangas KR, Chakravarti A, Moldin SO, Araj H, Blangero JC, Burmeister M, Crabbe J, Depaulo JR, Foulks E, Freimer NB, Koretz DS, Lichtenstein W, Mignot E, Reiss AL, Risch NJ, et al. Future of genetics of mood disorders research. Biological Psychiatry. 52: 457-77. PMID 12361664 DOI: 10.1016/S0006-3223(02)01471-3 |
0.379 |
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| 2002 |
Carrasquillo MM, McCallion AS, Puffenberger EG, Kashuk CS, Nouri N, Chakravarti A. Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease. Nature Genetics. 32: 237-44. PMID 12355085 DOI: 10.1038/Ng998 |
0.445 |
|
| 2002 |
Christian SL, McDonough J, Liu Cy CY, Shaikh S, Vlamakis V, Badner JA, Chakravarti A, Gershon ES. An evaluation of the assembly of an approximately 15-Mb region on human chromosome 13q32-q33 linked to bipolar disorder and schizophrenia. Genomics. 79: 635-56. PMID 11991713 DOI: 10.1006/Geno.2002.6765 |
0.374 |
|
| 2002 |
Chakravarti A. 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. 99: 4755-6. PMID 11959925 DOI: 10.1073/Pnas.092158299 |
0.419 |
|
| 2002 |
Marshall DG, Meier-Ruge WA, Chakravarti A, Langer JC. Chronic constipation due to Hirschsprung's disease and desmosis coli in a family. Pediatric Surgery International. 18: 110-4. PMID 11956774 DOI: 10.1007/S003830100682 |
0.334 |
|
| 2002 |
Gabriel SB, Salomon R, Pelet A, Angrist M, Amiel J, Fornage M, Attié-Bitach T, Olson JM, Hofstra R, Buys C, Steffann J, Munnich A, Lyonnet S, Chakravarti A. Segregation at three loci explains familial and population risk in Hirschsprung disease. Nature Genetics. 31: 89-93. PMID 11953745 DOI: 10.1038/Ng868 |
0.393 |
|
| 2002 |
Weese-Mayer DE, Bolk S, Silvestri JM, Chakravarti A. Idiopathic congenital central hypoventilation syndrome: Evaluation of brain-derived neurotrophic factor genomic DNA sequence variation American Journal of Medical Genetics. 107: 306-310. PMID 11840487 DOI: 10.1002/Ajmg.10133 |
0.386 |
|
| 2002 |
Kashuk C, SenGupta S, Eichler E, Chakravarti A. ViewGene: a graphical tool for polymorphism visualization and characterization. Genome Research. 12: 333-8. PMID 11827953 DOI: 10.1101/Gr.211202 |
0.386 |
|
| 2002 |
Zhu X, Cooper RS, Luke A, Chen G, Wu X, Kan D, Chakravarti A, Weder A. A genome-wide scan for obesity in African-Americans. Diabetes. 51: 541-4. PMID 11812767 DOI: 10.2337/Diabetes.51.2.541 |
0.346 |
|
| 2002 |
Boerwinkle E, Brown CA, Carrejo M, Ferrell R, Hanis C, Hutchinson R, Kardia S, Sing C, Turner S, Weder A, Chakravarti A, Cooper R, Jacob H, NS, Hunt S, et al. Multi-center genetic study of hypertension: The Family blood pressure program (FBPP) Hypertension. 39: 3-9. PMID 11799070 DOI: 10.1161/Hy1201.100415 |
0.331 |
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| 2001 |
Cutler DJ, Zwick ME, Carrasquillo MM, Yohn CT, Tobin KP, Kashuk C, Mathews DJ, Shah NA, Eichler EE, Warrington JA, Chakravarti A. High-throughput variation detection and genotyping using microarrays. Genome Research. 11: 1913-25. PMID 11691856 DOI: 10.1101/Gr.197201 |
0.795 |
|
| 2001 |
Mathews DJ, Kashuk C, Brightwell G, Eichler EE, Chakravarti A. Sequence variation within the fragile X locus. Genome Research. 11: 1382-91. PMID 11483579 DOI: 10.1101/Gr.172601 |
0.722 |
|
| 2001 |
Green ED, Chakravarti A. The human genome sequence expedition: views from the "base camp". Genome Research. 11: 645-51. PMID 11337462 DOI: 10.1101/Gr.188701 |
0.351 |
|
| 2001 |
Wiesner GL, Platzer P, Buxbaum S, Lewis S, MacMillen M, Olechnowicz J, Willis J, Chakravarti A, Elston RC, Markowitz SD. Testing for Colon Neoplasia Susceptibility Variants at the Human COX2 Locus Journal of the National Cancer Institute. 93: 635-639. PMID 11309440 DOI: 10.1093/Jnci/93.8.635 |
0.366 |
|
| 2001 |
Chakravarti A. To a future of genetic medicine. Nature. 409: 822-3. PMID 11236997 DOI: 10.1038/35057281 |
0.377 |
|
| 2001 |
Wiesner GL, Platzer P, Buxbaum SG, Lewis S, Macmillen M, Willis J, Chakravarti A, Elston RC, Markowitz SD. RESPONSE: Testing for Colon Neoplasia Susceptibility Variants at the Human COX2 Locus Jnci Journal of the National Cancer Institute. 93: 1573-1574. DOI: 10.1093/Jnci/93.20.1573 |
0.31 |
|
| 2000 |
Zwick ME, Cutler DJ, Chakravarti A. Patterns of genetic variation in Mendelian and complex traits. Annual Review of Genomics and Human Genetics. 1: 387-407. PMID 11701635 DOI: 10.1146/Annurev.Genom.1.1.387 |
0.778 |
|
| 2000 |
Schork NJ, Nath SK, 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. 67: 1208-18. PMID 11032785 DOI: 10.1086/321201 |
0.41 |
|
| 2000 |
Lynn A, Kashuk C, Petersen MB, Bailey JA, Cox DR, Antonarakis SE, Chakravarti A. Patterns of meiotic recombination on the long arm of human chromosome 21 Genome Research. 10: 1319-1332. PMID 10984450 DOI: 10.1101/Gr.138100 |
0.333 |
|
| 2000 |
Schork NJ, Chakravarti A, Thiel B, Fornage M, Jacob HJ, Cai R, Rotimi CN, Cooper RS, Weder AB. Lack of association between a biallelic polymorphism in the adducin gene and blood pressure in whites and African Americans. American Journal of Hypertension. 13: 693-8. PMID 10912755 DOI: 10.1016/S0895-7061(00)00237-5 |
0.363 |
|
| 2000 |
Fan JB, Chen X, Halushka MK, Berno A, Huang X, Ryder T, Lipshutz RJ, Lockhart DJ, Chakravarti A. Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays. Genome Research. 10: 853-60. PMID 10854416 DOI: 10.1101/Gr.10.6.853 |
0.612 |
|
| 2000 |
Bailey JA, Carrel L, Chakravarti A, Eichler EE. 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. 97: 6634-9. PMID 10841562 DOI: 10.1073/Pnas.97.12.6634 |
0.315 |
|
| 2000 |
Zaragoza MV, Surti U, Redline RW, Millie E, Chakravarti A, Hassold TJ. Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole. American Journal of Human Genetics. 66: 1807-20. PMID 10801385 DOI: 10.1086/302951 |
0.326 |
|
| 2000 |
Bolk S, Pelet A, Hofstra RM, Angrist M, Salomon R, Croaker D, Buys CH, 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. 97: 268-73. PMID 10618407 DOI: 10.1073/Pnas.97.1.268 |
0.367 |
|
| 1999 |
Halushka MK, Mathews DJ, Bailey JA, Chakravarti A. GIST: A web tool for collecting gene information. Physiological Genomics. 1: 75-81. PMID 11015564 DOI: 10.1152/Physiolgenomics.1999.1.2.75 |
0.773 |
|
| 1999 |
Jönsson EG, Nimgaonkar VL, Zhang XR, Shaw SH, Burgert E, Crocq MA, Chakravarti A, Sedvall GC. Trend for an association between schizophrenia and D3S1310, a marker in proximity to the dopamine D3 receptor gene. American Journal of Medical Genetics. 88: 352-7. PMID 10402502 DOI: 10.1002/(Sici)1096-8628(19990820)88:4<352::Aid-Ajmg12>3.0.Co;2-0 |
0.347 |
|
| 1999 |
Halushka MK, Fan JB, 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. 22: 239-47. PMID 10391210 DOI: 10.1038/10297 |
0.626 |
|
| 1999 |
Chakravarti A. 1998 ASHG Award for Excellence in Education. Professor Ching Chun Li, courageous scholar and educator. American Journal of Human Genetics. 64: 14-15. PMID 10075610 DOI: 10.1086/302224 |
0.333 |
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| 1999 |
Hong HK, Lass JH, 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. 8: 625-37. PMID 10072431 DOI: 10.1093/Hmg/8.4.625 |
0.33 |
|
| 1999 |
Kibar Z, Lafrenière RG, Chakravarti A, Wang JC, Chevrette M, Der Kaloustian VM, Rouleau GA. A radiation hybrid map of 48 loci including the clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q. Genomics. 56: 127-30. PMID 10036193 DOI: 10.1006/Geno.1998.5698 |
0.384 |
|
| 1999 |
Chakravarti A. Population genetics--making sense out of sequence. Nature Genetics. 21: 56-60. PMID 9915503 DOI: 10.1038/4482 |
0.41 |
|
| 1999 |
Southard-Smith EM, Angrist M, Ellison JS, Agarwala R, Baxevanis AD, Chakravarti A, Pavan WJ. The Sox10Dom Mouse: Modeling the Genetic Variation of Waardenburg-Shah (WS4) Syndrome Genome Research. 9: 215-225. DOI: 10.1101/Gr.9.3.215 |
0.422 |
|
| 1999 |
Chakravarti A. Identifying disease alleles by genome sharing Nature Genetics. 23: 25-25. DOI: 10.1038/14248 |
0.385 |
|
| 1998 |
Angrist M, Bolk S, Bentley K, Nallasamy S, Halushka MK, 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. 17: 3065-70. PMID 9881709 DOI: 10.1038/Sj.Onc.1202226 |
0.601 |
|
| 1998 |
Collins FS, Brooks LD, Chakravarti A. A DNA polymorphism discovery resource for research on human genetic variation Genome Research. 8: 1229-1231. PMID 9872978 DOI: 10.1101/Gr.8.12.1229 |
0.443 |
|
| 1998 |
Collins FS, 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.). 282: 682-9. PMID 9784121 DOI: 10.1126/Science.282.5389.682 |
0.32 |
|
| 1998 |
Blouin JL, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G, Thornquist M, Ullrich G, McGrath J, Kasch L, Lamacz M, Thomas MG, Gehrig C, Radhakrishna U, Snyder SE, ... ... Chakravarti A, et al. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nature Genetics. 20: 70-3. PMID 9731535 DOI: 10.1038/1734 |
0.314 |
|
| 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. 51: 417-26. PMID 9721212 DOI: 10.1006/Geno.1998.5389 |
0.369 |
|
| 1998 |
Brown DM, Matise TC, Koike G, Simon JS, Winer ES, Zangen S, McLaughlin MG, Shiozawa M, Atkinson OS, Hudson JR, Chakravarti A, Lander ES, Jacob HJ. An integrated genetic linkage map of the laboratory rat. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 521-30. PMID 9657848 DOI: 10.1007/S003359900812 |
0.349 |
|
| 1998 |
Angrist M, Jing S, Bolk S, Bentley K, Nallasamy S, Halushka M, Fox GM, Chakravarti A. Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility. Genomics. 48: 354-62. PMID 9545641 DOI: 10.1006/Geno.1997.5191 |
0.614 |
|
| 1998 |
Shaw SH, Carrasquillo MM, Kashuk C, Puffenberger EG, Chakravarti A. Allele frequency distributions in pooled DNA samples: Applications to mapping complex disease genes Genome Research. 8: 111-123. PMID 9477339 DOI: 10.1101/Gr.8.2.111 |
0.373 |
|
| 1998 |
Petersen MB, 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. 52: 247-8. PMID 9383032 DOI: 10.1111/J.1399-0004.1997.Tb02556.X |
0.335 |
|
| 1997 |
Collins FS, Guyer MS, Chakravarti A. Variations on a theme: Cataloging human DNA sequence variation Science. 278: 1580-1581. PMID 9411782 DOI: 10.1126/Science.278.5343.1580 |
0.398 |
|
| 1997 |
Carrasquillo MM, 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. 6: 2163-2172. PMID 9328482 DOI: 10.1093/Hmg/6.12.2163 |
0.422 |
|
| 1997 |
Cohen T, Zeitune M, McGillivray BC, Hall JG, Lynn AH, Aston CE, Chakravarti A. Segregation analysis of microcephaly. American Journal of Medical Genetics. 65: 226-34. PMID 9240749 DOI: 10.1002/(Sici)1096-8628(19961028)65:3<226::Aid-Ajmg11>3.0.Co;2-Q |
0.357 |
|
| 1997 |
Chen H, Rossier C, Nakamura Y, Lynn A, Chakravarti A, Antonarakis SE. Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3. Genomics. 41: 193-200. PMID 9143494 DOI: 10.1006/Geno.1997.4632 |
0.396 |
|
| 1997 |
Boguski M, Chakravarti A, Gibbs R, Green E, Myers RM. The end of the beginning: the race to begin human genome sequencing. Genome Research. 6: 771-2. PMID 8889545 DOI: 10.1101/Gr.6.9.771 |
0.317 |
|
| 1996 |
Nimgaonkar VL, Sanders AR, Ganguli R, Zhang XR, Brar J, Hogge W, Fann WE, Patel PI, Chakravarti A. Association Study of Schizophrenia and the Dopamine D3 Receptor Gene Locus in Two Independent Samples American Journal of Medical Genetics - Seminars in Medical Genetics. 67: 505-514. PMID 8950407 DOI: 10.1002/(Sici)1096-8628(19961122)67:6<505::Aid-Ajmg1>3.0.Co;2-G |
0.307 |
|
| 1996 |
Angrist M, Bolk S, Halushka M, Lapchak PA, Chakravarti A. Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient. Nature Genetics. 14: 341-4. PMID 8896568 DOI: 10.1038/Ng1196-341 |
0.57 |
|
| 1996 |
Eichler EE, Macpherson JN, Murray A, Jacobs PA, Chakravarti A, Nelson DL. 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. 5: 319-30. PMID 8852655 DOI: 10.1093/Hmg/5.3.319 |
0.39 |
|
| 1996 |
Bolk S, Angrist M, Schwartz S, Silvestri JM, Weese-Mayer DE, Chakravarti A. Congenital central hypoventilation syndrome: Mutation analysis of the receptor tyrosine kinase ret American Journal of Medical Genetics - Seminars in Medical Genetics. 63: 603-609. PMID 8826440 DOI: 10.1002/(Sici)1096-8628(19960628)63:4<603::Aid-Ajmg14>3.0.Co;2-M |
0.359 |
|
| 1996 |
Hofstra RM, Osinga J, Tan-Sindhunata G, Wu Y, Kamsteeg EJ, Stulp RP, van Ravenswaaij-Arts C, Majoor-Krakauer D, Angrist M, Chakravarti A, Meijers C, Buys CH. A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome). Nature Genetics. 12: 445-7. PMID 8630503 DOI: 10.1038/Ng0496-445 |
0.319 |
|
| 1996 |
Antonarakis SE, Blouin JL, Curran M, Luebbert H, Kazazian HH, Dombroski B, Housman D, Ton C, Karayiorgou M, Chakravarti A, Wolyniec P, Lasseter VK, Nestadt G, Pulver AE. Linkage and sib-pair analysis reveal a potential schizophrenia susceptibility gene on chromosome 13q32 Psychiatric Genetics. 6: 136. DOI: 10.1097/00041444-199623000-00009 |
0.311 |
|
| 1995 |
Talbot CC, Avramopouls D, Gerken S, Chakravarti A, Armour JA, Matsunami N, White R, Antonarakis SE. The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells Human Molecular Genetics. 4: 1193-1199. PMID 8528208 DOI: 10.1093/Hmg/4.7.1193 |
0.426 |
|
| 1995 |
Scott JA, Wenger SL, Steele MW, Chakravarti A. Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation. American Journal of Medical Genetics. 56: 67-71. PMID 7747789 DOI: 10.1002/Ajmg.1320560115 |
0.305 |
|
| 1995 |
Angrist M, Bolk S, Thiel B, Puffenberger EG, Hofstra RM, Buys CH, Cass DT, Chakravarti A. Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease. Human Molecular Genetics. 4: 821-30. PMID 7633441 DOI: 10.1093/Hmg/4.5.821 |
0.34 |
|
| 1994 |
Li CC, Chakravarti A. DNA profile similarity in a subdivided population. Human Heredity. 44: 100-9. PMID 8188309 DOI: 10.1159/000154199 |
0.314 |
|
| 1994 |
Samec S, Clarkson SG, Blaschak J, Chakravarti A, Morris MA, Scherly D, Antonarakis SE. Dinucleotide repeat polymorphism within ERCC5 gene. Human Molecular Genetics. 3: 214. PMID 8162040 DOI: 10.1093/Hmg/3.1.214-A |
0.36 |
|
| 1994 |
Matise TC, Perlin M, Chakravarti A. Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map. Nature Genetics. 6: 384-90. PMID 8054979 DOI: 10.1038/Ng0494-384 |
0.373 |
|
| 1994 |
Matise TC, Perlin M, Chakravarti A. Erratum: Corrigendum: Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map Nature Genetics. 7: 215-215. DOI: 10.1038/Ng0694-215B |
0.367 |
|
| 1993 |
Hong HK, Giorda R, Yu LM, Trucco M, Chakravarti A. Microsatellite repeat polymorphism at the D13S197 locus. Human Molecular Genetics. 2: 337. PMID 8499932 DOI: 10.1093/Hmg/2.3.337-A |
0.382 |
|
| 1993 |
Mutirangura A, Greenberg F, Butler MG, Malcolm S, Nicholls RD, Chakravarti A, Ledbetter DH. 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. 2: 143-51. PMID 8499903 DOI: 10.1093/Hmg/2.2.143 |
0.34 |
|
| 1993 |
Hong HK, Giorda R, Trucco M, Chakravarti A. Dinucleotide repeat polymorphisms at the D13S192 and D13S193 loci. Human Molecular Genetics. 2: 86. PMID 8490629 DOI: 10.1093/Hmg/2.1.86 |
0.387 |
|
| 1993 |
Warren AC, McInnis MG, Kalaitsidaki M, Cox TK, Blaschak J, Chakravarti A, Antonarakis SE. D21S210: A highly polymorphic (GT)n marker closely linked to the β-amyloid protein precursor (APP) gene Human Genetics. 91: 87-88. PMID 8454294 DOI: 10.1007/Bf00230232 |
0.365 |
|
| 1993 |
Avramopoulos D, Chakravarti A, Antonarakis SE. DNA polymorphisms in the 3' untranslated region of genes on human chromosome 21. Genomics. 15: 98-102. PMID 8432556 DOI: 10.1006/Geno.1993.1015 |
0.429 |
|
| 1993 |
Hong HK, Giorda R, Trucco M, Chakravarti A. Dinucleotide repeat polymorphism at the DXS1146 locus. Human Molecular Genetics. 2: 1078. PMID 8364552 DOI: 10.1093/Hmg/2.7.1078 |
0.369 |
|
| 1993 |
McInnis MG, Chakravarti A, Blaschak J, Petersen MB, Sharma V, Avramopoulos D, Blouin JL, König U, Brahe C, Matise TC. A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM. Genomics. 16: 562-71. PMID 8325627 DOI: 10.1006/Geno.1993.1231 |
0.344 |
|
| 1993 |
Delabar JM, Créau N, Sinet PM, Ritter O, Antonarakis SE, Burmeister M, Chakravarti A, Nizetic D, Ohki M, Patterson D. Report of the Fourth International Workshop on Human Chromosome 21. Genomics. 18: 735-45. PMID 8307590 DOI: 10.1016/S0888-7543(05)80390-8 |
0.327 |
|
| 1993 |
Washington SS, Bowcock AM, Gerken S, Matsunami N, Lesh D, Osborne-Lawrence SL, Cowell J, Ledbetter DH, White RL, Chakravarti A. A somatic cell hybrid map of human chromosome 13. Genomics. 18: 486-95. PMID 8307557 DOI: 10.1016/S0888-7543(11)80004-2 |
0.333 |
|
| 1993 |
Perlin M, Chakravarti A. Efficient construction of high-resolution physical maps from yeast artificial chromosomes using radiation hybrids: inner product mapping. Genomics. 18: 283-9. PMID 8288231 DOI: 10.1006/Geno.1993.1467 |
0.322 |
|
| 1993 |
Bowcock A, Osborne-Lawrence S, Barnes R, Chakravarti A, Washington S, Dunn C. Microsatellite polymorphism linkage map of human chromosome 13q. Genomics. 15: 376-86. PMID 8095487 DOI: 10.1006/Geno.1993.1071 |
0.377 |
|
| 1993 |
Avramopoulos D, Cox T, Kraus JP, Chakravarti A, Antonarakis SE. Linkage mapping of the cystathionine beta-synthase (CBS) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region. Human Genetics. 90: 566-8. PMID 8094069 DOI: 10.1007/Bf00217460 |
0.392 |
|
| 1993 |
Kalaitsidaki M, Cox T, Chakravarti A, Antonarakis SE. Cloning and linkage mapping of three polymorphic tetranucleotide (TAAA)n repeats on human chromosome 21. Genomics. 14: 1071-5. PMID 1478649 DOI: 10.1016/S0888-7543(05)80131-4 |
0.401 |
|
| 1992 |
Warren AC, Antonarakis SE, Chakravarti A. Chromosome 21 genetic linkage data set based on CEPH pedigrees Cytogenetic and Genome Research. 59: 86-87. PMID 1737517 DOI: 10.1159/000133207 |
0.363 |
|
| 1992 |
McInnis MG, Lutfalla G, Slaugenhaupt S, Petersen MB, Uze G, Chakravarti A, Antonarakis SE. Linkage mapping of highly informative DNA polymorphisms within the human interferon-alpha receptor gene on chromosome 21. Genomics. 11: 573-6. PMID 1685477 DOI: 10.1016/0888-7543(91)90064-L |
0.393 |
|
| 1992 |
Avramopoulos D, Cox T, Forrest GL, Chakravarti A, Antonarakis SE. Linkage mapping of the carbonyl reductase (CBR) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region. Genomics. 13: 447-8. PMID 1612603 DOI: 10.1016/0888-7543(92)90268-W |
0.384 |
|
| 1992 |
Warren AC, Petersen MB, Van Hul W, McInnis MG, Van Broeckhoven C, Cox TK, Chakravarti A, Antonarakis SE. D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21 Genomics. 13: 1365-1367. PMID 1505976 DOI: 10.1016/0888-7543(92)90072-Z |
0.4 |
|
| 1992 |
Warren AC, McInnis MG, Blaschak J, Kaliatsidaki M, Petersen MB, Chakravarti A, Antonarakis SE. Dinucleotide repeat (GT)n markers on chromosome 21 Genomics. 14: 818-819. PMID 1427915 DOI: 10.1016/S0888-7543(05)80198-3 |
0.388 |
|
| 1992 |
Avramopoulos D, Cox T, Blaschak JE, Chakravarti A, Antonarakis SE. Linkage mapping of the AML1 gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region. Genomics. 14: 506-7. PMID 1427868 DOI: 10.1016/S0888-7543(05)80253-8 |
0.375 |
|
| 1992 |
Hopper JL, Macaskill GT, Powles JW, Ktenas D, Chakravarti A. Pedigree analysis of blood pressure in subjects from rural Greece and relatives who migrated to Melbourne, Australia. Genetic Epidemiology. 9: 225-238. PMID 1398043 DOI: 10.1002/Gepi.1370090402 |
0.315 |
|
| 1992 |
Nimgaonkar VL, Ganguli R, Washington SS, Chakravarti A. Schizophrenia and porphobilinogen deaminase gene polymorphisms: an association study Schizophrenia Research. 8: 51-58. PMID 1358185 DOI: 10.1016/0920-9964(92)90060-I |
0.312 |
|
| 1992 |
Nimgaonkar V, Washington S, Ganguli R, Grandchamp B, Chakravarti A. An association study of schizophrenia and the porphobilinogen deaminase gene alleles Schizophrenia Research. 6: 90-91. DOI: 10.1016/0920-9964(92)90087-L |
0.304 |
|
| 1992 |
Chakravarti A, Mulvihill JJ. Genetic Epidemiology and genetic Epidemiology Genetic Epidemiology. 9: i-ii. DOI: 10.1002/Gepi.1370090102 |
0.342 |
|
| 1991 |
Chakravarti A. Information content of the Centre d'Etude du Polymorphisme Humain (CEPH) family structures for linkage studies. Human Genetics. 87: 721-4. PMID 1937475 DOI: 10.1007/Bf00201732 |
0.3 |
|
| 1991 |
Petersen MB, Weber JL, Slaugenhaupt SA, Kwitek AE, McInnis MG, Chakravarti A, Antonarakis SE. Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat. Human Genetics. 87: 401-4. PMID 1879826 DOI: 10.1007/Bf00197156 |
0.365 |
|
| 1991 |
Lupski JR, de Oca-Luna RM, Slaugenhaupt S, Pentao L, Guzzetta V, Trask BJ, Saucedo-Cardenas O, Barker DF, Killian JM, Garcia CA, Chakravarti A, Patel PI. DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell. 66: 219-32. PMID 1677316 DOI: 10.1016/0092-8674(91)90613-4 |
0.412 |
|
| 1991 |
Petersen MB, Slaugenhaupt SA, Lewis JG, Warren AC, Chakravarti A, Antonarakis SE. A genetic linkage map of 27 markers on human chromosome 21 Genomics. 9: 407-419. PMID 1674496 DOI: 10.1016/0888-7543(91)90406-5 |
0.377 |
|
| 1990 |
Badner JA, Chakravarti A. Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene. American Journal of Medical Genetics. 35: 100-4. PMID 2301458 DOI: 10.1002/Ajmg.1320350119 |
0.34 |
|
| 1990 |
Lewis JG, Weber JL, Petersen MB, Slaugenhaupt SA, Kwitek A, May PE, Warren AC, Chakravarti A, Antonarakis SE. Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat. Genomics. 8: 400-2. PMID 1979059 DOI: 10.1016/0888-7543(90)90300-J |
0.365 |
|
| 1990 |
Neiswanger K, Slaugenhaupt SA, Hughes HB, Frank E, Frankel DR, McCarty MJ, Chakravarti A, Zubenko GS, Kupfer DJ, Kaplan BB. Evidence against close linkage of unipolar affective illness to human chromosome 11p markers HRAS1 and INS and chromosome Xq marker DXS52 Biological Psychiatry. 28: 63-72. PMID 1973904 DOI: 10.1016/0006-3223(90)90433-3 |
0.36 |
|
| 1990 |
Petersen MB, Economou EP, Slaugenhaupt SA, Chakravarti A, Antonarakis SE. Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker. Genomics. 7: 136-8. PMID 1970797 DOI: 10.1016/0888-7543(90)90531-X |
0.417 |
|
| 1990 |
Long JC, Chakravarti A, Boehm CD, Antonarakis S, Kazazian HH. Phylogeny of human beta-globin haplotypes and its implications for recent human evolution. American Journal of Physical Anthropology. 81: 113-30. PMID 1967905 DOI: 10.1002/Ajpa.1330810112 |
0.362 |
|
| 1989 |
Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, Chakravarti A, Buchwald M, Tsui LC. Identification of the cystic fibrosis gene: genetic analysis. Science (New York, N.Y.). 245: 1073-80. PMID 2570460 DOI: 10.1126/Science.2570460 |
0.365 |
|
| 1989 |
Warren AC, Slaugenhaupt SA, Lewis JG, Chakravarti A, Antonarakis SE. A genetic linkage map of 17 markers on human chromosome 21 Genomics. 4: 579-591. PMID 2568330 DOI: 10.1016/0888-7543(89)90282-6 |
0.362 |
|
| 1988 |
Antonarakis SE, Oettgen P, Chakravarti A, Halloran SL, Hudson RR, Feisee L, Karathanasis SK. DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster Human Genetics. 80: 265-273. PMID 2903847 DOI: 10.1007/Bf01790095 |
0.394 |
|
| 1987 |
Chakravarti A, Badner JA, Li CC. Tests of linkage and heterogeneity in Mendelian diseases using identity by descent scores Genetic Epidemiology. 4: 255-266. PMID 3666434 DOI: 10.1002/Gepi.1370040404 |
0.312 |
|
| 1987 |
Chakravarti A, Slaugenhaupt SA. Methods for studying recombination on chromosomes that undergo nondisjunction. Genomics. 1: 35-42. PMID 3478296 DOI: 10.1016/0888-7543(87)90102-9 |
0.317 |
|
| 1987 |
Buetow KH, Chakravarti A, Cole SA. A genetic map of human chromosome 11p. Genetic Epidemiology. Supplement. 1: 135-40. PMID 3471656 DOI: 10.1002/Gepi.1370030721 |
0.357 |
|
| 1987 |
Kittur S, Lubs ML, Bauer M, Chakravarti A, Kazazian H. Linkage analysis of neurofibromatosis. Journal of Medical Genetics. 24: 526-527. PMID 3118030 DOI: 10.1136/Jmg.24.9.526 |
0.327 |
|
| 1987 |
Warren AC, Chakravarti A, Wong C, Slaugenhaupt SA, Halloran SL, Watkins PC, Metaxotou C, Antonarakis SE. Evidence for reduced recombination on the nondisjoined chromosomes 21 in down syndrome Science. 237: 652-654. PMID 2955519 DOI: 10.1126/Science.2955519 |
0.322 |
|
| 1987 |
Badner JA, Chakravarti A, Buetow KH. Linkage analysis between Huntington disease and the G8 marker locus. Genetic Epidemiology. Supplement. 1: 211-6. PMID 2883077 DOI: 10.1002/Gepi.1370030732 |
0.306 |
|
| 1986 |
Chakravarti A, Halloran SL, Bale SJ, Tucker MA. Etiological heterogeneity in Hodgkin's disease: HLA linked and unlinked determinants of susceptibility independent of histological concordance Genetic Epidemiology. 3: 407-415. PMID 3803911 DOI: 10.1002/Gepi.1370030605 |
0.321 |
|
| 1986 |
Chakravarti A, Elbein SC, Permutt MA. 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. 83: 1045-9. PMID 3006026 DOI: 10.1073/Pnas.83.4.1045 |
0.429 |
|
| 1985 |
Hafez M, Chakravarti A, el-Shennawy F, el-Morsi Z, el-Sallab SH, Al-Tonbary Y. HLA antigens and acute rheumatic fever: evidence for a recessive susceptibility gene linked to HLA. Genetic Epidemiology. 2: 273-82. PMID 4054602 DOI: 10.1002/Gepi.1370020305 |
0.331 |
|
| 1985 |
ANTONARAKIS SE, KITTUR SD, METAXOTOU C, BARTSOCAS C, KITSIOU S, WATKINS PC, PATEL AS, WARREN AC, GUSELLA JF, GRONER Y, CHAKRAVARTI A, MEYERS DA, KAZAZIAN HH. Linkage Map on Chromosome 21q and the Association of a DNA Haplotype with a Propensity to Nondisjunction and Trisomy 21 Annals of the New York Academy of Sciences. 450: 95-107. PMID 2990311 DOI: 10.1111/J.1749-6632.1985.Tb21486.X |
0.316 |
|
| 1985 |
Matteson KJ, Ostrer H, Chakravarti A, Buetow KH, O'Brien WE, Beaudet AL, Phillips JA. A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locus Human Genetics. 69: 263-267. PMID 2984106 DOI: 10.1007/Bf00293037 |
0.365 |
|
| 1985 |
Kittur S, Antonarakis S, Tanzi R, Meyers D, Chakravarti A, Groner Y, Phillips J, Watkins P, Gusella J, Kazazian H. A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21. The Embo Journal. 4: 2257-2260. DOI: 10.1002/J.1460-2075.1985.Tb03923.X |
0.407 |
|
| 1984 |
Badner JA, Chakravarti A, Wagener DK, Rao DC. A test of nonrandom segregation Genetic Epidemiology. 1: 329-340. PMID 6599403 DOI: 10.1002/Gepi.1370010405 |
0.409 |
|
| 1984 |
Chakravarti A, Phillips JA, Mellits KH, Buetow KH, Seeburg PH. 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. 81: 6085-9. PMID 6091133 DOI: 10.1073/Pnas.81.19.6085 |
0.372 |
|
| 1983 |
Daiger SP, Chakravarti A. Deletion mapping of polymorphic loci by apparent parental exclusion. American Journal of Medical Genetics. 14: 43-8. PMID 6299101 DOI: 10.1002/Ajmg.1320140108 |
0.379 |
|
| 1981 |
Ferrell RE, Hittner HM, Chakravarti A. Autosomal dominant cone-rod dystrophy: a linkage study with 17 biochemical and serological markers. American Journal of Medical Genetics. 8: 363-9. PMID 6940444 DOI: 10.1002/Ajmg.1320080316 |
0.313 |
|
| 1980 |
Ferrell RE, Chakravarti A, Hittner HM, Riccardi VM. 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. 77: 1580-2. PMID 6929510 DOI: 10.1073/Pnas.77.3.1580 |
0.355 |
|
| 1978 |
Malhotra KC, Chakraborty R, Chakravarti A. Gene differentiation among the Dhangar caste-cluster of Maharashtra, India. Human Heredity. 28: 26-36. PMID 618815 DOI: 10.1159/000152927 |
0.376 |
|
| 1977 |
Chakraborty R, Chakravarti A, Malhotra KC. Variation in allele frequencies among caste groups of the Dhangars of Maharashtra, India: an analysis with Wright's Fst statistic. Annals of Human Biology. 4: 275-80. PMID 900891 DOI: 10.1080/03014467700007162 |
0.373 |
|
| 1977 |
Nei M, Chakravarti A. Drift variances of FST and GST statistics obtained from a finite number of isolated populations. Theoretical Population Biology. 11: 307-25. PMID 877909 DOI: 10.1016/0040-5809(77)90014-4 |
0.549 |
|
| 1977 |
Nei M, Chakravarti A, Tateno Y. Mean and variance of FST in a finite number of incompletely isolated populations. Theoretical Population Biology. 11: 291-306. PMID 877908 DOI: 10.1016/0040-5809(77)90013-2 |
0.519 |
|
| 1977 |
Chakraborty R, Chakravarti A. On consanguineous marriages and the genetic load Human Genetics. 36: 47-54. PMID 870410 DOI: 10.1007/Bf00390435 |
0.336 |
|
| 1977 |
Chakravarti A. Genetic differentiation in the colonising lizard Anolis grahami Heredity. 38: 121-123. DOI: 10.1038/Hdy.1977.14 |
0.365 |
|
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