Babak Alipanahi

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

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Babak Alipanahi

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Computational Biology Machine Learning


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
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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