Babak Alipanahi

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	Toutes	Depuis 2020
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Coauteurs

Brendan FreyFounder & CEO, Deep Genomics; Co-Founder, Vector Institute; Professor, University of TorontoAdresse e-mail validée de psi.toronto.edu
Andrew DelongAssistant Professor (former), Concordia UniversityAdresse e-mail validée de concordia.ca
Benjamin J. BlencoweProfessor, University of TorontoAdresse e-mail validée de utoronto.ca
Hui Yuan XiongRenaissance TechnologiesAdresse e-mail validée de psi.toronto.edu
Leo J. LeeSenior Research Scientist, University of TorontoAdresse e-mail validée de psi.toronto.edu
Daniele MericoVevo Tx / TCAG (SickKids)Adresse e-mail validée de vevo.ai
Hannes BretschneiderDonnelly Centre and Department of Molecular Genetics, University of TorontoAdresse e-mail validée de utoronto.ca
Scherer, Stephen W.The Hospital for Sick Children, Genetics and Genome Biology Program, University of TorontoAdresse e-mail validée de sickkids.ca
Ryan K.C. YuenSenior Scientist, Hospital for Sick ChildrenAdresse e-mail validée de sickkids.ca
Matthew T. WeirauchProfessor, Cincinnati Children's HospitalAdresse e-mail validée de cchmc.org
Michael K.K. LeungPhD, University of TorontoAdresse e-mail validée de mail.utoronto.ca
Ali GhodsiProfessor of Statistics and Computer Science, University of WaterlooAdresse e-mail validée de uwaterloo.ca
Manuel IrimiaCentre for Genomic RegulationAdresse e-mail validée de crg.eu
Nuno Barbosa-MoraisResearch Group Leader, Instituto de Medicina Molecular - LisbonAdresse e-mail validée de medicina.ulisboa.pt
Logan DonaldsonProfessor of Biology, York UniversityAdresse e-mail validée de yorku.ca
Hamed S. NajafabadiAssociate Professor at McGill UniversityAdresse e-mail validée de mcgill.ca
Timothy R. HughesUniversity of TorontoAdresse e-mail validée de utoronto.ca
Quaid MorrisComputational and Systems Biology Program, Memorial Sloan Kettering Cancer CenterAdresse e-mail validée de mskcc.org
Serge GueroussovPostdoctoral associate, Broad InstituteAdresse e-mail validée de broadinstitute.org
Nebojsa JojicMicrosoft ResearchAdresse e-mail validée de microsoft.com

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Babak Alipanahi

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Adresse e-mail validée de exai.bio - Page d'accueil

Computational Biology Machine Learning


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
Predicting the sequence specificities of DNA-and RNA-binding proteins by deep learning B Alipanahi, A Delong, MT Weirauch, BJ Frey Nature biotechnology 33 (8), 831-838, 2015	3225	2015
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019	1935	2019
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use M Liu, Y Jiang, R Wedow, 23andMe Research Team Nat Genet 51 (2), 237-244, 2019	1742	2019
The human splicing code reveals new insights into the genetic determinants of disease HY Xiong, B Alipanahi, LJ Lee, H Bretschneider, D Merico, RKC Yuen, ... Science 347 (6218), 1254806, 2015	1493	2015
Underspecification presents challenges for credibility in modern machine learning A D'Amour, K Heller, D Moldovan, B Adlam, B Alipanahi, A Beutel, ... Journal of Machine Learning Research 23 (226), 1-61, 2022	818	2022
Widespread intron retention in mammals functionally tunes transcriptomes U Braunschweig, NL Barbosa-Morais, Q Pan, EN Nachman, B Alipanahi, ... Genome research 24 (11), 1774-1786, 2014	715	2014
An atlas of genetic influences on osteoporosis in humans and mice JA Morris, JP Kemp, SE Youlten, L Laurent, JG Logan, RC Chai, ... Nature genetics 51 (2), 258-266, 2019	699	2019
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences R Karlsson Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, ... Nature genetics 51 (2), 245-257, 2019	684	2019
Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine DJ Stavropoulos, D Merico, R Jobling, S Bowdin, N Monfared, ... NPJ genomic medicine 1 (1), 1-9, 2016	398	2016
MBNL proteins repress ES-cell-specific alternative splicing and reprogramming H Han, M Irimia, PJ Ross, HK Sung, B Alipanahi, L David, A Golipour, ... Nature 498 (7453), 241-245, 2013	356	2013
Machine learning in genomic medicine: a review of computational problems and data sets MKK Leung, A Delong, B Alipanahi, BJ Frey Proceedings of the IEEE 104 (1), 176-197, 2015	354	2015
Genome-wide characteristics of de novo mutations in autism RKC Yuen, D Merico, H Cao, G Pellecchia, B Alipanahi, ... NPJ genomic medicine 1 (1), 1-10, 2016	246	2016
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis B Schormair, C Zhao, S Bell, E Tilch, AV Salminen, B Pütz, Y Dauvilliers, ... The Lancet Neurology 16 (11), 898-907, 2017	234	2017
Are random forests truly the best classifiers? M Wainberg, B Alipanahi, BJ Frey Journal of Machine Learning Research 17 (110), 1-5, 2016	208	2016
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ... Biological psychiatry 83 (12), 1044-1053, 2018	197	2018
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder M Uddin, K Tammimies, G Pellecchia, B Alipanahi, P Hu, Z Wang, D Pinto, ... Nature genetics 46 (7), 742-747, 2014	178	2014
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells EL Bao, SK Nandakumar, X Liao, AG Bick, J Karjalainen, M Tabaka, ... Nature 586 (7831), 769-775, 2020	126	2020
Systems and methods for classifying, prioritizing and interpreting genetic variants and therapies using a deep neural network B Frey, MKK Leung, AT Delong, HY Xiong, B Alipanahi, LJ Lee, ... US Patent 10,185,803, 2019	112	2019
Common variant burden contributes to the familial aggregation of migraine in 1,589 families P Gormley, MI Kurki, ME Hiekkala, K Veerapen, P Häppölä, AA Mitchell, ... Neuron 98 (4), 743-753. e4, 2018	108	2018
The effect of LRRK2 loss-of-function variants in humans N Whiffin, IM Armean, A Kleinman, JL Marshall, EV Minikel, JK Goodrich, ... Nature Medicine 26 (6), 869-877, 2020	106	2020

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