Works by Craig, David W.

Results: 76
    1

    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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    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
    5

    Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 873, doi. 10.1038/ng.419
    By:
    • Skibola, Christine F.;
    • Bracci, Paige M.;
    • Halperin, Eran;
    • Conde, Lucia;
    • Craig, David W.;
    • Agana, Luz;
    • Iyadurai, Kelly;
    • Becker, Nikolaus;
    • Brooks-Wilson, Angela;
    • Curry, John D.;
    • Spinelli, John J.;
    • Holly, Elizabeth A.;
    • Riby, Jacques;
    • Luoping Zhang;
    • Nieters, Alexandra;
    • Smith, Martyn T.;
    • Brown, Kevin M.
    Publication type:
    Article
    6

    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
    7

    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
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    Multi-modality machine learning predicting Parkinson's disease.

    Published in:
    NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00288-w
    By:
    • Makarious, Mary B.;
    • Leonard, Hampton L.;
    • Vitale, Dan;
    • Iwaki, Hirotaka;
    • Sargent, Lana;
    • Dadu, Anant;
    • Violich, Ivo;
    • Hutchins, Elizabeth;
    • Saffo, David;
    • Bandres-Ciga, Sara;
    • Kim, Jonggeol Jeff;
    • Song, Yeajin;
    • Maleknia, Melina;
    • Bookman, Matt;
    • Nojopranoto, Willy;
    • Campbell, Roy H.;
    • Hashemi, Sayed Hadi;
    • Botia, Juan A.;
    • Carter, John F.;
    • Craig, David W.
    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
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    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
    15

    Corrigendum: Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4.

    Published in:
    Nature Genetics, 2014, v. 46, n. 7, p. 759, doi. 10.1038/ng0714-759a
    By:
    • Ramos, Pilar;
    • Karnezis, Anthony N;
    • Craig, David W;
    • Sekulic, Aleksander;
    • Russel, Megan L;
    • Hendricks, William P D;
    • Corneveaux, Jason J;
    • Barrett, Michael T;
    • Shumansky, Karey;
    • Yang, Yidong;
    • Shah, Sohrab P;
    • Prentice, Leah M;
    • Marra, Marco A;
    • Kiefer, Jeffrey;
    • Zismann, Victoria L;
    • McEachron, Troy A;
    • Salhia, Bodour;
    • Prat, Jaime;
    • D'Angelo, Emanuela;
    • Clarke, Blaise A
    Publication type:
    Article
    16

    Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4.

    Published in:
    Nature Genetics, 2014, v. 46, n. 5, p. 427, doi. 10.1038/ng.2928
    By:
    • Ramos, Pilar;
    • Karnezis, Anthony N;
    • Craig, David W;
    • Sekulic, Aleksandar;
    • Russell, Megan L;
    • Hendricks, William P D;
    • Corneveaux, Jason J;
    • Barrett, Michael T;
    • Shumansky, Karey;
    • Yang, Yidong;
    • Shah, Sohrab P;
    • Prentice, Leah M;
    • Marra, Marco A;
    • Kiefer, Jeffrey;
    • Zismann, Victoria L;
    • McEachron, Troy A;
    • Salhia, Bodour;
    • Prat, Jaime;
    • D'Angelo, Emanuela;
    • Clarke, Blaise A
    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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    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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    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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    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
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    Cancer of the ampulla of Vater: analysis of the whole genome sequence exposes a potential therapeutic vulnerability.

    Published in:
    Genome Medicine, 2012, v. 4, n. 7, p. 1, doi. 10.1186/gm357
    By:
    • Demeure, Michael J.;
    • Craig, David W.;
    • Sinari, Shripad;
    • Moses, Tracy M.;
    • Christoforides, Alexis;
    • Dinh, Jennifer;
    • Izatt, Tyler;
    • Aldrich, Jessica;
    • Decker, Ardis;
    • Baker, Angela;
    • Cherni, Irene;
    • Watanabe, April;
    • Koep, Lawrence;
    • Lake, Douglas;
    • Hostetter, Galen;
    • Trent, Jeffrey M.;
    • Von Hoff, Daniel D.;
    • Carpten, John D.
    Publication type:
    Article
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    A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41‐q42 deletion phenotype.

    Published in:
    American Journal of Medical Genetics. Part A, 2018, v. 176, n. 7, p. 1549, doi. 10.1002/ajmg.a.38712
    By:
    • Balak, Chris;
    • Belnap, Newell;
    • Ramsey, Keri;
    • Joss, Shelagh;
    • Devriendt, Koen;
    • Naymik, Marcus;
    • Jepsen, Wayne;
    • Siniard, Ashley L.;
    • Szelinger, Szabolcs;
    • Parker, Mary E.;
    • Richholt, Ryan;
    • Izatt, Tyler;
    • LaFleur, Madison;
    • Terraf, Panieh;
    • Llaci, Lorida;
    • De Both, Matt;
    • Piras, Ignazio S.;
    • Rangasamy, Sampathkumar;
    • Schrauwen, Isabelle;
    • Craig, David W.
    Publication type:
    Article
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    Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.

    Published in:
    Journal of Neural Transmission, 2008, v. 115, n. 11, p. 1573, doi. 10.1007/s00702-008-0119-3
    By:
    • Lesch, Klaus-Peter;
    • Timmesfeld, Nina;
    • Renner, Tobias J.;
    • Halperin, Rebecca;
    • Röser, Christoph;
    • Nguyen, T. Trang;
    • Craig, David W.;
    • Romanos, Jasmin;
    • Heine, Monika;
    • Meyer, Jobst;
    • Freitag, Christine;
    • Warnke, Andreas;
    • Romanos, Marcel;
    • Schäfer, Helmut;
    • Walitza, Susanne;
    • Reif, Andreas;
    • Stephan, Dietrich A.;
    • Jacob, Christian
    Publication type:
    Article
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    Identification of genetic variants using bar-coded multiplexed sequencing.

    Published in:
    Nature Methods, 2008, v. 5, n. 10, p. 887, doi. 10.1038/nmeth.1251
    By:
    • Craig, David W.;
    • Pearson, John V.;
    • Szelinger, Szabolcs;
    • Sekar, Aswin;
    • Redman, Margot;
    • Corneveaux, Jason J.;
    • Pawlowski, Traci L.;
    • Laub, Trisha;
    • Nunn, Gary;
    • Stephan, Dietrich A.;
    • Homer, Nils;
    • Huentelman, Matthew J.
    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
    42

    A Pilot Study Using Next-Generation Sequencing in Advanced Cancers: Feasibility and Challenges.

    Published in:
    PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0076438
    By:
    • Weiss, Glen J.;
    • Liang, Winnie S.;
    • Demeure, Michael J.;
    • Kiefer, Jeff A.;
    • Hostetter, Galen;
    • Izatt, Tyler;
    • Sinari, Shripad;
    • Christoforides, Alexis;
    • Aldrich, Jessica;
    • Kurdoglu, Ahmet;
    • Phillips, Lori;
    • Benson, Hollie;
    • Reiman, Rebecca;
    • Baker, Angela;
    • Marsh, Vickie;
    • Von Hoff, Daniel D.;
    • Carpten, John D.;
    • Craig, David W.
    Publication type:
    Article
    43

    Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing.

    Published in:
    PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0043192
    By:
    • Liang, Winnie S.;
    • Craig, David W.;
    • Carpten, John;
    • Borad, Mitesh J.;
    • Demeure, Michael J.;
    • Weiss, Glen J.;
    • Izatt, Tyler;
    • Sinari, Shripad;
    • Christoforides, Alexis;
    • Aldrich, Jessica;
    • Kurdoglu, Ahmet;
    • Barrett, Michael;
    • Phillips, Lori;
    • Benson, Hollie;
    • Tembe, Waibhav;
    • Braggio, Esteban;
    • Kiefer, Jeffrey A.;
    • Legendre, Christophe;
    • Posner, Richard;
    • Hostetter, Galen H.
    Publication type:
    Article
    44

    Paired Tumor and Normal Whole Genome Sequencing of Metastatic Olfactory Neuroblastoma.

    Published in:
    PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037029
    By:
    • Weiss, Glen J.;
    • Liang, Winnie S.;
    • Izatt, Tyler;
    • Arora, Shilpi;
    • Cherni, Irene;
    • Raju, Robert N.;
    • Hostetter, Galen;
    • Kurdoglu, Ahmet;
    • Christoforides, Alexis;
    • Sinari, Shripad;
    • Baker, Angela S.;
    • Metpally, Raghu;
    • Tembe, Waibhav D.;
    • Phillips, Lori;
    • Von Hoff, Daniel D.;
    • Craig, David W.;
    • Carpten, John D.
    Publication type:
    Article
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    Multiethnic PDX models predict a possible immune signature associated with TNBC of African ancestry.

    Published in:
    Breast Cancer Research & Treatment, 2021, v. 186, n. 2, p. 391, doi. 10.1007/s10549-021-06097-8
    By:
    • Jiagge, Evelyn M.;
    • Ulintz, Peter J.;
    • Wong, Shukmei;
    • McDermott, Sean P.;
    • Fossi, Sabrina I.;
    • Suhan, Tahra K.;
    • Hoenerhoff, Mark J.;
    • Bensenhaver, Jessica M.;
    • Salem, Barbara;
    • Dziubinski, Michele;
    • Oppong, Joseph K.;
    • Aitpillah, Francis;
    • Ishmael, Kyei;
    • Osei-Bonsu, Ernest;
    • Adjei, Ernest;
    • Baffour, Awuah;
    • Aldrich, Jessica;
    • Kurdoglu, Ahmet;
    • Fernando, Kurt;
    • Craig, David W.
    Publication type:
    Article
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