Works by Craig, David W.

Results: 75
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    Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations.

    Published in:
    Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 2, p. 1, doi. 10.1002/mgg3.1857
    By:
    • Ramsey, Keri;
    • Belnap, Newell;
    • Bonfitto, Anna;
    • Jepsen, Wayne;
    • Naymik, Marcus;
    • Sanchez‐Castillo, Meredith;
    • Craig, David W.;
    • Szelinger, Szabolcs;
    • Huentelman, Matthew J.;
    • Narayanan, Vinodh;
    • Rangasamy, Sampath
    Publication type:
    Article
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    Novel pathogenic variants and genes for myopathies identified by whole exome sequencing.

    Published in:
    Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 4, p. 283, doi. 10.1002/mgg3.142
    By:
    • Hunter, Jesse M.;
    • Ahearn, Mary Ellen;
    • Balak, Christopher D.;
    • Liang, Winnie S.;
    • Kurdoglu, Ahmet;
    • Corneveaux, Jason J.;
    • Russell, Megan;
    • Huentelman, Matthew J.;
    • Craig, David W.;
    • Carpten, John;
    • Coons, Stephen W.;
    • DeMello, Daphne E.;
    • Hall, Judith G.;
    • Bernes, Saunder M.;
    • Baumbach‐Reardon, Lisa
    Publication type:
    Article
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    Personalized treatment of Sézary syndrome by targeting a novel CTLA4:CD28 fusion.

    Published in:
    Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 2, p. 130, doi. 10.1002/mgg3.121
    By:
    • Sekulic, Aleksandar;
    • Liang, Winnie S.;
    • Tembe, Waibhav;
    • Izatt, Tyler;
    • Kruglyak, Semyon;
    • Kiefer, Jeffrey A.;
    • Cuyugan, Lori;
    • Zismann, Victoria;
    • Legendre, Christophe;
    • Pittelkow, Mark R.;
    • Gohmann, John J.;
    • De Castro, Fernando R.;
    • Trent, Jeffrey;
    • Carpten, John;
    • Craig, David W.;
    • McDaniel, Timothy K.
    Publication type:
    Article
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    Multi‐omic molecular profiling guide's efficacious treatment selection in refractory metastatic breast cancer: a prospective phase II clinical trial.

    Published in:
    Molecular Oncology, 2022, v. 16, n. 1, p. 104, doi. 10.1002/1878-0261.13091
    By:
    • Pierobon, Mariaelena;
    • Robert, Nicholas J.;
    • Northfelt, Donald W.;
    • Jahanzeb, Mohammad;
    • Wong, Shukmei;
    • Hodge, Kimberly A.;
    • Baldelli, Elisa;
    • Aldrich, Jessica;
    • Craig, David W.;
    • Liotta, Lance A.;
    • Avramovic, Sanja;
    • Wojtusiak, Janusz;
    • Alemi, Farrokh;
    • Wulfkuhle, Julia D.;
    • Bellos, Angela;
    • Gallagher, Rosa I.;
    • Arguello, David;
    • Conrad, Amber;
    • Kemkes, Ariane;
    • Loesch, David M.
    Publication type:
    Article
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    Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2010, v. 6, n. 3, p. 265, doi. 10.1016/j.jalz.2010.03.013
    By:
    • Saykin, Andrew J.;
    • Shen, Li;
    • Foroud, Tatiana M.;
    • Potkin, Steven G.;
    • Swaminathan, Shanker;
    • Kim, Sungeun;
    • Risacher, Shannon L.;
    • Nho, Kwangsik;
    • Huentelman, Matthew J.;
    • Craig, David W.;
    • Thompson, Paul M.;
    • Stein, Jason L.;
    • Moore, Jason H.;
    • Farrer, Lindsay A.;
    • Green, Robert C.;
    • Bertram, Lars;
    • Jack, Clifford R.;
    • Weiner, Michael W.
    Publication type:
    Article
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    Front Cover, Volume 41, Issue 2.

    Published in:
    Human Mutation, 2020, v. 41, n. 2, p. i, doi. 10.1002/humu.23982
    By:
    • McCullough, Carmel G.;
    • Szelinger, Szabolcs;
    • Belnap, Newell;
    • Ramsey, Keri;
    • Schrauwen, Isabelle;
    • Claasen, Ana M.;
    • Burke, Leah W.;
    • Siniard, Ashley L.;
    • Huentelman, Matthew J.;
    • Narayanan, Vinodh;
    • Craig, David W.
    Publication type:
    Article
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    Open-access synthetic spike-in mRNA-seq data for cancer gene fusions.

    Published in:
    BMC Genomics, 2014, v. 15, n. 1, p. 824, doi. 10.1186/1471-2164-15-824
    By:
    • Tembe, Waibhav D.;
    • Pond, Stephanie J. K.;
    • Legendre, Christophe;
    • Han-Yu Chuang;
    • Liang, Winnie S.;
    • Kim, Nancy E.;
    • Montel, Valerie;
    • Shukmei Wong;
    • McDaniel, Timothy K.;
    • Craig, David W.;
    • Carpten, John D.
    Publication type:
    Article
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    Common sequence variants on 20q11.22 confer melanoma susceptibility.

    Published in:
    Nature Genetics, 2008, v. 40, n. 7, p. 838, doi. 10.1038/ng.163
    By:
    • Brown, Kevin M.;
    • MacGregor, Stuart;
    • Montgomery, Grant W.;
    • Craig, David W.;
    • Zhen Zhen Zhao;
    • Iyadurai, Kelly;
    • Anjali K. Henders;
    • Homer, Nils;
    • Campbell, Megan J.;
    • Stark, Mitchell;
    • Thomas, Shane;
    • Schmid, Helen;
    • Holland, Elizabeth A.;
    • Gillanders, Elizabeth M.;
    • Duffy, David L.;
    • Maskiell, Judith A.;
    • Jetann, Jodie;
    • Ferguson, Megan;
    • Stephan, Dietrich A.;
    • Cust, Anne E.
    Publication type:
    Article
    23

    A survey of genetic human cortical gene expression.

    Published in:
    Nature Genetics, 2007, v. 39, n. 12, p. 1494, doi. 10.1038/ng.2007.16
    By:
    • Myers, Amanda J.;
    • Gibbs, J. Raphael;
    • Webster, Jennifer A.;
    • Rohrer, Kristen;
    • Zhao, Alice;
    • Marlowe, Lauren;
    • Kaleem, Mona;
    • Leung, Doris;
    • Bryden, Leslie;
    • Nath, Priti;
    • Zismann, Victoria L.;
    • Joshipura, Keta;
    • Huentelman, Matthew J.;
    • Hu-Lince, Diane;
    • Coon, Keith D.;
    • Craig, David W.;
    • Pearson, John V.;
    • Holmans, Peter;
    • Heward, Christopher B.;
    • Reiman, Eric M.
    Publication type:
    Article
    24

    Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD).

    Published in:
    Human Genetics, 2019, v. 138, n. 11/12, p. 1409, doi. 10.1007/s00439-019-02077-7
    By:
    • Llaci, Lorida;
    • Ramsey, Keri;
    • Belnap, Newell;
    • Claasen, Ana M.;
    • Balak, Chris D.;
    • Szelinger, Szabolcs;
    • Jepsen, Wayne M.;
    • Siniard, Ashley L.;
    • Richholt, Ryan;
    • Izat, Tyler;
    • Naymik, Marcus;
    • De Both, Matt;
    • Piras, Ignazio S.;
    • Craig, David W.;
    • Huentelman, Matthew J.;
    • Narayanan, Vinodh;
    • Schrauwen, Isabelle;
    • Rangasamy, Sampathkumar
    Publication type:
    Article
    25

    Toward precision medicine in glioblastoma: the promise and the challenges.

    Published in:
    Neuro-Oncology, 2015, v. 17, n. 8, p. 1051, doi. 10.1093/neuonc/nov031
    By:
    • Prados, Michael D.;
    • Byron, Sara A.;
    • Tran, Nhan L.;
    • Phillips, Joanna J.;
    • Molinaro, Annette M.;
    • Ligon, Keith L.;
    • Patrick Y. Wen;
    • Kuhn, John G.;
    • Mellinghoff, Ingo K.;
    • de Groot, John F.;
    • Colman, Howard;
    • Cloughesy, Timothy F.;
    • Chang, Susan M.;
    • Ryken, Timothy C.;
    • Tembe, Waibhav D.;
    • Kiefer, Jeffrey A.;
    • Berens, Michael E.;
    • Craig, David W.;
    • Carpten, John D.;
    • Trent, Jeffrey M.
    Publication type:
    Article
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    Sorl1 as an Alzheimer’s Disease Predisposition Gene?

    Published in:
    Neurodegenerative Diseases, 2008, v. 5, n. 2, p. 60, doi. 10.1159/000110789
    By:
    • Webster, Jennifer A.;
    • Myers, Amanda J.;
    • Pearson, John V.;
    • Craig, David W.;
    • Hu-Lince, Diane;
    • Coon, Keith D.;
    • Zismann, Victoria L.;
    • Beach, Thomas;
    • Leung, Doris;
    • Bryden, Leslie;
    • Halperin, Rebecca F.;
    • Marlowe, Lauren;
    • Kaleem, Mona;
    • Huentelman, Matthew J.;
    • Joshipura, Keta;
    • Walker, Douglas;
    • Heward, Christopher B.;
    • Ravid, Rivka;
    • Rogers, Joseph;
    • Papassotiropoulos, Andreas
    Publication type:
    Article
    32

    Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder.

    Published in:
    Journal of Neuroinflammation, 2013, v. 10, n. 1, p. 1, doi. 10.1186/1742-2094-10-38
    By:
    • Napolioni, Valerio;
    • Ober-Reynolds, Benjamin;
    • Szelinger, Szabolcs;
    • Corneveaux, Jason J.;
    • Pawlowski, Traci;
    • Ober-Reynolds, Sharman;
    • Kirwan, Janet;
    • Persico, Antonio M.;
    • Melmed, Raun D.;
    • Craig, David W.;
    • Smith, Christopher J.;
    • Huentelman, Matthew J.
    Publication type:
    Article
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    Polygenic risk for anxiety influences anxiety comorbidity and suicidal behavior in bipolar disorder.

    Published in:
    Translational Psychiatry, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41398-020-00981-5
    By:
    • Lopes, Fabiana L.;
    • Zhu, Kevin;
    • Purves, Kirstin L.;
    • Song, Christopher;
    • Ahn, Kwangmi;
    • Hou, Liping;
    • Akula, Nirmala;
    • Kassem, Layla;
    • Bergen, Sarah E.;
    • Landen, Mikael;
    • Veras, Andre B.;
    • Nardi, Antonio E.;
    • Bipolar Genome Study Consortium (BiGS);
    • Alliey-Rodriguez, Ney;
    • Badner, Judith A.;
    • Berrettini, Wade;
    • Byerley, William;
    • Coryell, William;
    • Craig, David W.;
    • Edenberg, Howard J.
    Publication type:
    Article
    38

    Bringing RNA-seq closer to the clinic.

    Published in:
    Nature Biotechnology, 2014, v. 32, n. 9, p. 884, doi. 10.1038/nbt.3017
    By:
    • Van Keuren-Jensen, Kendall;
    • Keats, Jonathan J;
    • Craig, David W
    Publication type:
    Article
    39

    Extramedullary myeloma whole genome sequencing reveals novel mutations in Cereblon, proteasome subunit G2 and the glucocorticoid receptor in multi drug resistant disease.

    Published in:
    British Journal of Haematology, 2013, v. 161, n. 5, p. 748, doi. 10.1111/bjh.12291
    By:
    • Egan, Jan B.;
    • Kortuem, K. Martin;
    • Kurdoglu, Ahmet;
    • Izatt, Tyler;
    • Aldrich, Jessica;
    • Reiman, Rebecca;
    • Phillips, Lori;
    • Baker, Angela;
    • Shi, Chang‐Xin;
    • Schmidt, Jessica;
    • Liang, Winnie S.;
    • Craig, David W.;
    • Carpten, John D.;
    • Stewart, A. Keith
    Publication type:
    Article
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    Identifying treatment options for BRAF<sup>V600</sup> wild-type metastatic melanoma: A SU2C/MRA genomics-enabled clinical trial.

    Published in:
    PLoS ONE, 2021, v. 16, n. 4, p. 1, doi. 10.1371/journal.pone.0248097
    By:
    • LoRusso, Patricia M.;
    • Sekulic, Aleksandar;
    • Sosman, Jeffrey A.;
    • Liang, Winnie S.;
    • Carpten, John;
    • Craig, David W.;
    • Solit, David B.;
    • Bryce, Alan H.;
    • Kiefer, Jeffrey A.;
    • Aldrich, Jessica;
    • Nasser, Sara;
    • Halperin, Rebecca;
    • Byron, Sara A.;
    • Pilat, Mary Jo;
    • Boerner, Scott A.;
    • Durecki, Diane;
    • Hendricks, William P. D.;
    • Enriquez, Daniel;
    • Izatt, Tyler;
    • Keats, Jonathan
    Publication type:
    Article
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    A somatic reference standard for cancer genome sequencing.

    Published in:
    Scientific Reports, 2016, p. 24607, doi. 10.1038/srep24607
    By:
    • Craig, David W.;
    • Nasser, Sara;
    • Corbett, Richard;
    • Chan, Simon K.;
    • Murray, Lisa;
    • Legendre, Christophe;
    • Tembe, Waibhav;
    • Adkins, Jonathan;
    • Kim, Nancy;
    • Wong, Shukmei;
    • Baker, Angela;
    • Enriquez, Daniel;
    • Pond, Stephanie;
    • Pleasance, Erin;
    • Mungall, Andrew J.;
    • Moore, Richard A.;
    • McDaniel, Timothy;
    • Ma, Yussanne;
    • Jones, Steven J. M.;
    • Marra, Marco A.
    Publication type:
    Article
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    Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 16, p. 3295, doi. 10.1093/hmg/ddq221
    By:
    • Corneveaux, Jason J.;
    • Myers, Amanda J.;
    • Allen, April N.;
    • Pruzin, Jeremy J.;
    • Ramirez, Manuel;
    • Engel, Anzhelika;
    • Nalls, Michael A.;
    • Chen, Kewei;
    • Lee, Wendy;
    • Chewning, Kendria;
    • Villa, Stephen E.;
    • Meechoovet, Hunsar B.;
    • Gerber, Jill D.;
    • Frost, Danielle;
    • Benson, Hollie L.;
    • O'Reilly, Sean;
    • Chibnik, Lori B.;
    • Shulman, Joshua M.;
    • Singleton, Andrew B.;
    • Craig, David W.
    Publication type:
    Article
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    Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance.

    Published in:
    Human Molecular Genetics, 2007, v. 16, n. 12, p. 1469, doi. 10.1093/hmg/ddm097
    By:
    • Huentelman, Matthew J.;
    • Papassotiropoulos, Andreas;
    • Craig, David W.;
    • Hoerndli, Frederic J.;
    • Pearson, John V.;
    • Huynh, Kim-Dung;
    • Corneveaux, Jason;
    • Hänggi, Jürgen;
    • Mondadori, Christian R.A.;
    • Buchmann, Andreas;
    • Reiman, Eric M.;
    • Henke, Katharina;
    • de Quervain, Dominique J.-F.;
    • Stephan, Dietrich A.
    Publication type:
    Article
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    Whole Genome Analyses of a Well-Differentiated Liposarcoma Reveals Novel <i>SYT1</i> and <i>DDR2</i> Rearrangements.

    Published in:
    PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0087113
    By:
    • Egan, Jan B.;
    • Barrett, Michael T.;
    • Champion, Mia D.;
    • Middha, Sumit;
    • Lenkiewicz, Elizabeth;
    • Evers, Lisa;
    • Francis, Princy;
    • Schmidt, Jessica;
    • Shi, Chang-Xin;
    • Van Wier, Scott;
    • Badar, Sandra;
    • Ahmann, Gregory;
    • Kortuem, K. Martin;
    • Boczek, Nicole J.;
    • Fonseca, Rafael;
    • Craig, David W.;
    • Carpten, John D.;
    • Borad, Mitesh J.;
    • Stewart, A. Keith
    Publication type:
    Article