Found: 72

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  • At-home Testing and Risk Factors for Acquisition of SARS-CoV-2 Infection in a Major US Metropolitan Area.

    Published in:
    Open Forum Infectious Diseases, 2022, v. 9, n. 11, p. 1, doi. 10.1093/ofid/ofac505
    By:
    • Woolley, Ann E;
    • Dryden-Peterson, Scott;
    • Kim, Andy;
    • Naz-McLean, Sarah;
    • Kelly, Christina;
    • Laibinis, Hannah H;
    • Bagnall, Josephine;
    • Livny, Jonathan;
    • Ma, Peijun;
    • Orzechowski, Marek;
    • Gomez, James;
    • Shoresh, Noam;
    • Gabriel, Stacey;
    • Hung, Deborah T;
    • Cosimi, Lisa A
    Publication type:
    Article

  • Performance and Operational Evaluation of the Access Bio CareStart Rapid Antigen Test in a High-Throughput Drive-Through Community Testing Site in Massachusetts.

    Published in:
    Open Forum Infectious Diseases, 2021, v. 8, n. 7, p. 1, doi. 10.1093/ofid/ofab243
    By:
    • Pollock, Nira R;
    • Tran, Kristine;
    • Jacobs, Jesica R;
    • Cranston, Amber E;
    • Smith, Sita;
    • O'Kane, Claire Y;
    • Roady, Tyler J;
    • Moran, Anne;
    • Scarry, Alison;
    • Carroll, Melissa;
    • Volinsky, Leila;
    • Perez, Gloria;
    • Patel, Pinal;
    • Gabriel, Stacey;
    • Lennon, Niall J;
    • Madoff, Lawrence C;
    • Brown, Catherine;
    • Smole, Sandra C
    Publication type:
    Article

  • Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study.

    Published in:
    Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-05415-4
    By:
    • Wang, Heming;
    • Kurniansyah, Nuzulul;
    • Cade, Brian E.;
    • Goodman, Matthew O.;
    • Chen, Han;
    • Gottlieb, Daniel J.;
    • Gharib, Sina A.;
    • Purcell, Shaun M.;
    • Lin, Xihong;
    • Saxena, Richa;
    • Zhu, Xiaofeng;
    • Durda, Peter;
    • Tracy, Russel;
    • Liu, Yongmei;
    • Taylor, Kent D.;
    • Johnson, W. Craig;
    • Gabriel, Stacey;
    • Smith, Joshua D.;
    • Aguet, François;
    • Ardlie, Kirstin
    Publication type:
    Article

  • Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy.

    Published in:
    Journal of Clinical Investigation, 2014, v. 124, n. 11, p. 4693, doi. 10.1172/JCI75199
    By:
    • Yuen, Michaela;
    • Sandaradura, Sarah A.;
    • Dowling, James J.;
    • Kostyukova, Alla S.;
    • Moroz, Natalia;
    • Quinlan, Kate G.;
    • Lehtokari, Vilma-Lotta;
    • Ravenscroft, Gianina;
    • Todd, Emily J.;
    • Ceyhan-Birsoy, Ozge;
    • Gokhin, David S.;
    • Maluenda, Jérome;
    • Lek, Monkol;
    • Nolent, Flora;
    • Pappas, Christopher T.;
    • Novak, Stefanie M.;
    • D'Amico, Adele;
    • Malfatti, Edoardo;
    • Thomas, Brett P.;
    • Gabriel, Stacey B.
    Publication type:
    Article

  • DGAT1 mutation is linked to a congenital diarrheal disorder.

    Published in:
    Journal of Clinical Investigation, 2012, v. 122, n. 12, p. 4680, doi. 10.1172/JCI64873
    By:
    • Haas, Joel T.;
    • Winter, Harland S.;
    • Elaine Lim;
    • Kirby, Andrew;
    • Blumenstie, Brendan;
    • DeFelice, Matthew;
    • Gabriel, Stacey;
    • Jalas, Chaim;
    • Branski, David;
    • Grueter, Carrie A.;
    • Toporovski, Mauro S.;
    • Walther, Tobias C.;
    • Daly, Mark J.;
    • Farese Jr., Robert V.
    Publication type:
    Article

  • Outbreak of SARS-CoV-2 Infections, Including COVID-19 Vaccine Breakthrough Infections, Associated with Large Public Gatherings - Barnstable County, Massachusetts, July 2021.

    Published in:
    2021
    By:
    • Brown, Catherine M.;
    • Vostok, Johanna;
    • Johnson, Hillary;
    • Burns, Meagan;
    • Gharpure, Radhika;
    • Sami, Samira;
    • Sabo, Rebecca T.;
    • Hall, Noemi;
    • Foreman, Anne;
    • Schubert, Petra L.;
    • Gallagher, Glen R.;
    • Fink, Timelia;
    • Madoff, Lawrence C.;
    • Gabriel, Stacey B.;
    • MacInnis, Bronwyn;
    • Park, Daniel J.;
    • Siddle, Katherine J.;
    • Harik, Vaira;
    • Arvidson, Deirdre;
    • Brock-Fisher, Taylor
    Publication type:
    journal article

  • Evaluation of the Access Bio CareStart rapid SARS-CoV-2 antigen test in asymptomatic individuals tested at a community mass-testing program in Western Massachusetts.

    Published in:
    Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-25266-3
    By:
    • Suliman, Sara;
    • Matias, Wilfredo R.;
    • Fulcher, Isabel R.;
    • Molano, Francisco J.;
    • Collins, Shannon;
    • Uceta, Elizabeth;
    • Zhu, Jack;
    • Paxton, Ryan M.;
    • Gonsalves, Sean F.;
    • Harden, Maegan V.;
    • Fisher, Marissa;
    • Meldrim, Jim;
    • Gabriel, Stacey;
    • Franke, Molly F.;
    • Hung, Deborah T.;
    • Smole, Sandra C.;
    • Madoff, Lawrence C.;
    • Ivers, Louise C.
    Publication type:
    Article

  • Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation.

    Published in:
    Nucleic Acids Research, 2013, v. 41, n. 6, p. e67, doi. 10.1093/nar/gks1443
    By:
    • Costello, Maura;
    • Pugh, Trevor J.;
    • Fennell, Timothy J.;
    • Stewart, Chip;
    • Lichtenstein, Lee;
    • Meldrim, James C.;
    • Fostel, Jennifer L.;
    • Friedrich, Dennis C.;
    • Perrin, Danielle;
    • Dionne, Danielle;
    • Kim, Sharon;
    • Gabriel, Stacey B.;
    • Lander, Eric S.;
    • Fisher, Sheila;
    • Getz, Gad
    Publication type:
    Article

  • PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 736, doi. 10.1002/ajmg.b.32688
    By:
    • Khalil, Raida;
    • Kenny, Connor;
    • Hill, R. Sean;
    • Mochida, Ganeshwaran H.;
    • Nasir, Ramzi;
    • Partlow, Jennifer N.;
    • Barry, Brenda J.;
    • Al‐Saffar, Muna;
    • Egan, Chloe;
    • Stevens, Christine R.;
    • Gabriel, Stacey B.;
    • Barkovich, A. James;
    • Ellison, Jay W.;
    • Al‐Gazali, Lihadh;
    • Walsh, Christopher A.;
    • Chahrour, Maria H.
    Publication type:
    Article

  • Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01031-z
    By:
    • Venner, Eric;
    • Muzny, Donna;
    • Smith, Joshua D.;
    • Walker, Kimberly;
    • Neben, Cynthia L.;
    • Lockwood, Christina M.;
    • Empey, Phillip E.;
    • Metcalf, Ginger A.;
    • Kachulis, Chris;
    • Mian, Sana;
    • Musick, Anjene;
    • Rehm, Heidi L.;
    • Harrison, Steven;
    • Gabriel, Stacey;
    • Gibbs, Richard A.;
    • Nickerson, Deborah;
    • Zhou, Alicia Y.;
    • Doheny, Kimberly;
    • Ozenberger, Bradley;
    • Topper, Scott E.
    Publication type:
    Article

  • Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

    Published in:
    Nature Biotechnology, 2013, v. 31, n. 3, p. 213, doi. 10.1038/nbt.2514
    By:
    • Cibulskis, Kristian;
    • Lawrence, Michael S;
    • Carter, Scott L;
    • Sivachenko, Andrey;
    • Jaffe, David;
    • Sougnez, Carrie;
    • Gabriel, Stacey;
    • Meyerson, Matthew;
    • Lander, Eric S;
    • Getz, Gad
    Publication type:
    Article

  • Combinatorics and next-generation sequencing.

    Published in:
    Nature Biotechnology, 2009, v. 27, n. 9, p. 826, doi. 10.1038/nbt0909-826
    By:
    • Patterson, Nick;
    • Gabriel, Stacey
    Publication type:
    Article

  • Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing.

    Published in:
    Nature Biotechnology, 2009, v. 27, n. 2, p. 182, doi. 10.1038/nbt.1523
    By:
    • Gnirke, Andreas;
    • Melnikov, Alexandre;
    • Maguire, Jared;
    • Rogov, Peter;
    • LeProust, Emily M;
    • Brockman, William;
    • Fennell, Timothy;
    • Giannoukos, Georgia;
    • Fisher, Sheila;
    • Russ, Carsten;
    • Gabriel, Stacey;
    • Jaffe, David B;
    • Lander, Eric S;
    • Nusbaum, Chad
    Publication type:
    Article

  • Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.

    Published in:
    Nature Genetics, 2015, v. 47, n. 5, p. 528, doi. 10.1038/ng.3256
    By:
    • Akizu, Naiara;
    • Ozgul, R Koksal;
    • Sagıroglu, Mahmut Samil;
    • Azam, Matloob;
    • Selim, Laila;
    • Mahmoud, Iman G;
    • Abdel-Hadi, Sawsan;
    • Badawy, Amera El;
    • Sadek, Abdelrahim A;
    • Mojahedi, Faezeh;
    • Kayserili, Hulya;
    • Masri, Amira;
    • Bastaki, Laila;
    • Müller, Ulrich;
    • Cantagrel, Vincent;
    • Desguerre, Isabelle;
    • Casanova, Jean-Laurent;
    • Dursun, Ali;
    • Gunel, Murat;
    • Gabriel, Stacey B
    Publication type:
    Article

  • RNF43 is frequently mutated in colorectal and endometrial cancers.

    Published in:
    Nature Genetics, 2014, v. 46, n. 12, p. 1264, doi. 10.1038/ng.3127
    By:
    • Giannakis, Marios;
    • Van Allen, Eliezer M;
    • Hahn, William C;
    • Garraway, Levi A;
    • Fuchs, Charles S;
    • Hodis, Eran;
    • Jasmine Mu, Xinmeng;
    • Rosenbluh, Joseph;
    • Yamauchi, Mai;
    • Qian, Zhi Rong;
    • Cibulskis, Kristian;
    • Saksena, Gordon;
    • Lawrence, Michael S;
    • Gabriel, Stacey B;
    • Nishihara, Reiko;
    • Lander, Eric S;
    • Getz, Gad;
    • Ogino, Shuji
    Publication type:
    Article

  • A framework for the interpretation of de novo mutation in human disease.

    Published in:
    Nature Genetics, 2014, v. 46, n. 9, p. 944, doi. 10.1038/ng.3050
    By:
    • Samocha, Kaitlin E;
    • Robinson, Elise B;
    • Sanders, Stephan J;
    • Stevens, Christine;
    • Sabo, Aniko;
    • McGrath, Lauren M;
    • Kosmicki, Jack A;
    • Rehnström, Karola;
    • Mallick, Swapan;
    • Kirby, Andrew;
    • Wall, Dennis P;
    • MacArthur, Daniel G;
    • Gabriel, Stacey B;
    • DePristo, Mark;
    • Purcell, Shaun M;
    • Palotie, Aarno;
    • Boerwinkle, Eric;
    • Buxbaum, Joseph D;
    • Cook, Edwin H;
    • Gibbs, Richard A
    Publication type:
    Article

  • Pan-cancer patterns of somatic copy number alteration.

    Published in:
    Nature Genetics, 2013, v. 45, n. 10, p. 1134, doi. 10.1038/ng.2760
    By:
    • Zack, Travis I;
    • Schumacher, Steven E;
    • Carter, Scott L;
    • Cherniack, Andrew D;
    • Saksena, Gordon;
    • Tabak, Barbara;
    • Lawrence, Michael S;
    • Zhang, Cheng-Zhong;
    • Wala, Jeremiah;
    • Mermel, Craig H;
    • Sougnez, Carrie;
    • Gabriel, Stacey B;
    • Hernandez, Bryan;
    • Shen, Hui;
    • Laird, Peter W;
    • Getz, Gad;
    • Meyerson, Matthew;
    • Beroukhim, Rameen
    Publication type:
    Article

  • De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly.

    Published in:
    Nature Genetics, 2012, v. 44, n. 8, p. 941, doi. 10.1038/ng.2329
    By:
    • Lee, Jeong Ho;
    • Huynh, My;
    • Silhavy, Jennifer L;
    • Kim, Sangwoo;
    • Dixon-Salazar, Tracy;
    • Heiberg, Andrew;
    • Scott, Eric;
    • Bafna, Vineet;
    • Hill, Kiley J;
    • Collazo, Adrienne;
    • Funari, Vincent;
    • Russ, Carsten;
    • Gabriel, Stacey B;
    • Mathern, Gary W;
    • Gleeson, Joseph G
    Publication type:
    Article

  • Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.

    Published in:
    Nature Genetics, 2011, v. 43, n. 8, p. 801, doi. 10.1038/ng.871
    By:
    • Shea, Jessica;
    • Agarwala, Vineeta;
    • Philippakis, Anthony A;
    • Maguire, Jared;
    • Banks, Eric;
    • DePristo, Mark;
    • Thomson, Brian;
    • Guiducci, Candace;
    • Onofrio, Robert C.;
    • M. I. G.C.;
    • Kathiresan, Sekar;
    • Gabriel, Stacey;
    • Burtt, Noël P.;
    • Daly, Mark J.;
    • Groop, Leif;
    • Altshuler, David
    Publication type:
    Article

  • A framework for variation discovery and genotyping using next-generation DNA sequencing data.

    Published in:
    Nature Genetics, 2011, v. 43, n. 5, p. 491, doi. 10.1038/ng.806
    By:
    • DePristo, Mark A.;
    • Banks, Eric;
    • Poplin, Ryan;
    • Garimella, Kiran V.;
    • Maguire, Jared R.;
    • Hartl, Christopher;
    • Philippakis, Anthony A.;
    • del Angel, Guillermo;
    • Rivas, Manuel A.;
    • Hanna, Matt;
    • McKenna, Aaron;
    • Fennell, Tim J.;
    • Kernytsky, Andrew M.;
    • Sivachenko, Andrey Y.;
    • Cibulskis, Kristian;
    • Gabriel, Stacey B.;
    • Altshuler, David;
    • Daly, Mark J.
    Publication type:
    Article

  • High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 851, doi. 10.1038/ng.659
    By:
    • Calvo, Sarah E.;
    • Tucker, Elena J.;
    • Compton, Alison G.;
    • Kirby, Denise M.;
    • Crawford, Gabriel;
    • Burtt, Noel P.;
    • Rivas, Manuel;
    • Guiducci, Candace;
    • Bruno, Damien L.;
    • Goldberger, Olga A.;
    • Redman, Michelle C.;
    • Wiltshire, Esko;
    • Wilson, Callum J.;
    • Altshuler, David;
    • Gabriel, Stacey B.;
    • Daly, Mark J.;
    • Thorburn, David R.;
    • Mootha, Vamsi K.
    Publication type:
    Article

  • Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes.

    Published in:
    Nature Genetics, 2010, v. 42, n. 7, p. 619, doi. 10.1038/ng.594
    By:
    • Valente, Enza Maria;
    • Logan, Clare V;
    • Mougou-Zerelli, Soumaya;
    • Lee, Jeong Ho;
    • Silhavy, Jennifer L;
    • Brancati, Francesco;
    • Iannicelli, Miriam;
    • Travaglini, Lorena;
    • Romani, Sveva;
    • Illi, Barbara;
    • Adams, Matthew;
    • Szymanska, Katarzyna;
    • Mazzotta, Annalisa;
    • Ji Eun Lee;
    • Tolentino, Jerlyn C;
    • Swistun, Dominika;
    • Salpietro, Carmelo D;
    • Fede, Carmelo;
    • Gabriel, Stacey;
    • Russ, Carsten
    Publication type:
    Article

  • De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 931, doi. 10.1038/ng.415
    By:
    • Greenway, Steven C.;
    • Pereira, Alexandre C.;
    • Lin, Jennifer C.;
    • DePalma, Steven R.;
    • Israel, Samuel J.;
    • Mesquita, Sonia M.;
    • Ergul, Emel;
    • Conta, Jessie H.;
    • Korn, Joshua M.;
    • McCarroll, Steven A.;
    • Gorham, Joshua M.;
    • Gabriel, Stacey;
    • Altshuler, David M.;
    • Quintanilla-Dieck, Maria de Lourdes;
    • Artunduaga, Maria Alexandra;
    • Eavey, Roland D.;
    • Plenge, Robert M.;
    • Shadick, Nancy A.;
    • Weinblatt, Michael E.;
    • De Jager, Philip L.
    Publication type:
    Article

  • Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 35, doi. 10.1038/ng.271
    By:
    • Sabatti, Chiara;
    • Service, Susan K.;
    • Hartikainen, Anna-Liisa;
    • Pouta, Anneli;
    • Ripatti, Samuli;
    • Brodsky, Jae;
    • Jones, Chris G.;
    • Zaitlen, Noah A.;
    • Varilo, Teppo;
    • Kaakinen, Marika;
    • Sovio, Ulla;
    • Ruokonen, Aimo;
    • Laitinen, Jaana;
    • Jakkula, Eveliina;
    • Coin, Lachlan;
    • Hoggart, Clive;
    • Collins, Andrew;
    • Turunen, Hannu;
    • Gabriel, Stacey;
    • Elliot, Paul
    Publication type:
    Article

  • Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.

    Published in:
    Nature Genetics, 2008, v. 40, n. 10, p. 1253, doi. 10.1038/ng.237
    By:
    • Korn, Joshua M.;
    • Kuruvilla, Finny G.;
    • McCarroll, Steven A.;
    • Wysoker, Alec;
    • Nemesh, James;
    • Cawley, Simon;
    • Hubbell, Earl;
    • Veitch, Jim;
    • Collins, Patrick J.;
    • Darvishi, Katayoon;
    • Lee, Charles;
    • Nizzari, Marcia M.;
    • Gabriel, Stacey B.;
    • Purcell, Shaun;
    • Daly, Mark J.;
    • Altshuler, David
    Publication type:
    Article

  • Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 204, doi. 10.1038/ng.81
    By:
    • Harley, John B.;
    • Alarcón-Riquelme, Marta E.;
    • Criswell, Lindsey A.;
    • Jacob, Chaim O.;
    • Kimberly, Robert P.;
    • Moser, Kathy L.;
    • Tsao, Betty P.;
    • Vyse, Timothy J.;
    • Langefeld, Carl D.;
    • Nath, Swapan K.;
    • Guthridge, Joel M.;
    • Cobb, Beth L.;
    • Mirel, Daniel B.;
    • Marion, Miranda C.;
    • Williams, Adrienne H.;
    • Divers, Jasmin;
    • Wei Wang;
    • Frank, Summer G.;
    • Namjou, Bahram;
    • Gabriel, Stacey B.
    Publication type:
    Article

  • New models of collaboration in genome-wide association studies: the Genetic Association Information Network.

    Published in:
    Nature Genetics, 2007, v. 39, n. 9, p. 1045, doi. 10.1038/ng2127
    By:
    • Manolio, Teri A.;
    • Rodriguez, Laura Lyman;
    • Brooks, Lisa;
    • Abecasis, Gonçalo;
    • Ballinger, Dennis;
    • Daly, Mark;
    • Donnelly, Peter;
    • Faraone, Stephen V.;
    • Frazer, Kelly;
    • Gabriel, Stacey;
    • Gejman, Pablo;
    • Guttmacher, Alan;
    • Harris, Emily L.;
    • Insel, Thomas;
    • Kelsoe, John R.;
    • Lander, Eric;
    • McCowin, Norma;
    • Mailman, Matthew D.;
    • Nabel, Elizabeth;
    • Ostell, James
    Publication type:
    Article

  • Corrigendum: High-throughput oncogene mutation profiling in human cancer.

    Published in:
    2007
    By:
    • Thomas, Roman K.;
    • Baker, Alissa C.;
    • DeBiasi, Ralph M.;
    • Winckler, Wendy;
    • LaFramboise, Thomas;
    • Lin, William M.;
    • Wang, Meng;
    • Feng, Whei;
    • Zander, Thomas;
    • MacConnaill, Laura E.;
    • Lee, Jeffrey C.;
    • Nicoletti, Rick;
    • Hatton, Charlie;
    • Goyette, Mary;
    • Girard, Luc;
    • Majmudar, Kuntal;
    • Ziaugra, Liuda;
    • Wong, Kwok-Kin;
    • Gabriel, Stacey;
    • Beroukhim, Rameen
    Publication type:
    Correction Notice

  • High-throughput oncogene mutation profiling in human cancer.

    Published in:
    Nature Genetics, 2007, v. 39, n. 3, p. 347, doi. 10.1038/ng1975
    By:
    • Thomas, Roman K.;
    • Baker, Alissa C.;
    • DeBiasi, Ralph M.;
    • Winckler, Wendy;
    • LaFramboise, Thomas;
    • Lin, William M.;
    • Meng Wang;
    • Whei Feng;
    • Zander, Thomas;
    • MacConnaill, Laura E.;
    • Lee, Jeffrey C.;
    • Nicoletti, Rick;
    • Hatton, Charlie;
    • Goyette, Mary;
    • Girard, Luc;
    • Majmudar, Kuntal;
    • Ziaugra, Liuda;
    • Kwok-Kin Wong;
    • Gabriel, Stacey;
    • Beroukhim, Rameen
    Publication type:
    Article

  • Common deletion polymorphisms in the human genome.

    Published in:
    Nature Genetics, 2006, v. 38, n. 1, p. 86, doi. 10.1038/ng1696
    By:
    • McCarroll, Steven A.;
    • Hadnott, Tracy N.;
    • Perry, George H.;
    • Sabeti, Pardis C.;
    • Zody, Michael C.;
    • Barrett, Jeffrey C.;
    • Dallaire, Stephanie;
    • Gabriel, Stacey B.;
    • Lee, Charles;
    • Daly, Mark J.;
    • Altshuler, David M.
    Publication type:
    Article

  • Efficiency and power in genetic association studies.

    Published in:
    Nature Genetics, 2005, v. 37, n. 11, p. 1217, doi. 10.1038/ng1669
    By:
    • de Bakker, Paul I. W.;
    • Yelensky, Roman;
    • Pe'er, Itsik;
    • Gabriel, Stacey B.;
    • Daly, Mark J.;
    • Altshuler, David
    Publication type:
    Article

  • Assessing the impact of population stratification on genetic association studies.

    Published in:
    Nature Genetics, 2004, v. 36, n. 4, p. 388, doi. 10.1038/ng1333
    By:
    • Freedman, Matthew L.;
    • Reich, David;
    • Penney, Kathryn L.;
    • McDonald, Gavin J.;
    • Mignault, Andre A.;
    • Patterson, Nick;
    • Gabriel, Stacey B.;
    • Topol, Eric J.;
    • Smoller, Jordan W.;
    • Pato, Carlos N.;
    • Pato, Michele T.;
    • Petryshen, Tracey L.;
    • Kolonel, Laurence N.;
    • Lander, Eric S.;
    • Sklar, Pamela;
    • Henderson, Brian;
    • Hirschhorn, Joel N.;
    • Altshuler, David
    Publication type:
    Article

  • Quality and completeness of SNP databases.

    Published in:
    Nature Genetics, 2003, v. 33, n. 4, p. 457, doi. 10.1038/ng1133
    By:
    • Reich, David E.;
    • Gabriel, Stacey B.;
    • Altshuler, David
    Publication type:
    Article

  • Segregation at three loci explains familial and population risk in Hirschsprung disease.

    Published in:
    Nature Genetics, 2002, v. 31, n. 1, p. 89, doi. 10.1038/ng868
    By:
    • Gabriel, Stacey Bolk;
    • Salomon, Rémi;
    • Pelet, Anna;
    • Angrist, Misha;
    • Amiel, Jeanne;
    • Fornage, Myriam;
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  • THE P53 PATHWAY AND ANCESTRAL PROGENITORS ARE ASSOCIATED WITH TUMOR RECURRENCE IN GLIOBLASTOMA.

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  • Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.

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  • Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction.

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  • Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.

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  • High-throughput RNA isoform sequencing using programmed cDNA concatenation.

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