Works matching AU Craig, David W.

Results: 75

Transcriptome analysis provides critical answers to the "variants of uncertain significance" conundrum.

Published in:

Human Mutation, 2022, v. 43, n. 11, p. 1590, doi. 10.1002/humu.24394

By:

Postel, Mackenzie D.;
Culver, Julie O.;
Ricker, Charité;
Craig, David W.

Publication type:

Article

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

Utilizing RNA and outlier analysis to identify an intronic splice‐altering variant in AP4S1 in a sibling pair with progressive spastic paraplegia.

Published in:

Human Mutation, 2020, v. 41, n. 2, p. 412, doi. 10.1002/humu.23939

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

SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays.

Published in:

Bioinformatics, 2007, v. 23, n. 1, p. 57, doi. 10.1093/bioinformatics/btl536

By:

Jianping Hua;
David W. Craig;
Marcel Brun;
Jennifer Webster;
Victoria Zismann;
Waibhav Tembe;
Keta Joshipura;
Matthew J. Huentelman;
Edward R. Dougherty;
Dietrich A. Stephan

Publication type:

Article

A method to reduce ancestry related germline false positives in tumor only somatic variant calling.

Published in:

BMC Medical Genomics, 2017, v. 10, p. 1, doi. 10.1186/s12920-017-0296-8

By:

Halperin, Rebecca F.;
Carpten, John D.;
Manojlovic, Zarko;
Aldrich, Jessica;
Keats, Jonathan;
Byron, Sara;
Liang, Winnie S.;
Russell, Megan;
Enriquez, Daniel;
Claasen, Ana;
Cherni, Irene;
Awuah, Baffour;
Oppong, Joseph;
Wicha, Max S.;
Newman, Lisa A.;
Jaigge, Evelyn;
Seungchan Kim;
Craig, David W.

Publication type:

Article

Whole genome sequencing reveals potential targets for therapy in patients with refractory KRAS mutated metastatic colorectal cancer.

Published in:

BMC Medical Genomics, 2014, v. 7, n. 1, p. 3, doi. 10.1186/1755-8794-7-36

By:

Shanmugam, Vijayalakshmi;
Ramanathan, Ramesh K.;
Lavender, Nicole A.;
Sinari, Shripad;
Chadha, Manpreet;
Liang, Winnie S.;
Kurdoglu, Ahmet;
Izatt, Tyler;
Christoforides, Alexis;
Benson, Hollie;
Phillips, Lori;
Baker, Angela;
Murray, Christopher;
Hostetter, Galen;
Von Hoff, Daniel D.;
Craig, David W.;
Carpten, John D.

Publication type:

Article

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

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

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

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

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

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

Identification of disease causing loci using an array-based genotyping approach on pooled DNA.

Published in:

BMC Genomics, 2005, v. 6, p. 138, doi. 10.1186/1471-2164-6-138

By:

Craig, David W;
Huentelman, Matthew J;
Hu-Lince, Diane;
Zismann, Victoria L;
Kruer, Michael C;
Lee, Anne M;
Puffenberger, Erik G;
Pearson, John M;
Stephan, Dietrich A

Publication type:

Article

SNiPer: Improved SNP genotype calling for Affymetrix 10K GeneChip microarray data.

Published in:

BMC Genomics, 2005, v. 6, p. 149, doi. 10.1186/1471-2164-6-149

By:

Huentelman, Matthew J;
Craig, David W;
Shieh, Albert D;
Corneveaux, Jason J;
Hu-Lince, Diane;
Pearson, John V;
Stephan, Dietrich A

Publication type:

Article

Dystonia in ATP2B3-associated X-linked spinocerebellar ataxia.

Published in:

2016

By:

Feyma, Timothy;
Ramsey, Keri;
Huentelman, Matthew J.;
Craig, David W.;
Padilla ‐ Lopez, Sergio;
Narayanan, Vinodh;
Kruer, Michael C.;
C4RCD Research Group;
Padilla-Lopez, Sergio

Publication type:

Case Study

A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome.

Published in:

PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0131797

By:

Schrauwen, Isabelle;
Szelinger, Szabolcs;
Siniard, Ashley L.;
Kurdoglu, Ahmet;
Corneveaux, Jason J.;
Malenica, Ivana;
Richholt, Ryan;
Van Camp, Guy;
De Both, Matt;
Swaminathan, Shanker;
Turk, Mari;
Ramsey, Keri;
Craig, David W.;
Narayanan, Vinodh;
Huentelman, Matthew J.

Publication type:

Article

Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing.

Published in:

PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0113036

By:

Szelinger, Szabolcs;
Malenica, Ivana;
Corneveaux, Jason J.;
Siniard, Ashley L.;
Kurdoglu, Ahmet A.;
Ramsey, Keri M.;
Schrauwen, Isabelle;
Trent, Jeffrey M.;
Narayanan, Vinodh;
Huentelman, Matthew J.;
Craig, David W.

Publication type:

Article

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

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

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

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

Autism and Increased Paternal Age Related Changes in Global Levels of Gene Expression Regulation.

Published in:

PLoS ONE, 2011, v. 6, n. 2, p. 1, doi. 10.1371/journal.pone.0016715

By:

Alter, Mark D.;
Kharkar, Rutwik;
Ramsey, Keri E.;
Craig, David W.;
Melmed, Raun D.;
Grebe, Theresa A.;
Bay, R. Curtis;
Ober-Reynolds, Sharman;
Kirwan, Janet;
Jones, Josh J.;
Turner, J. Blake;
Hen, Rene;
Stephan, Dietrich A.

Publication type:

Article

Identification of a Novel Risk Locus for Multiple Sclerosis at 13q31.3 by a Pooled Genome-Wide Scan of 500,000 Single Nucleotide Polymorphisms.

Published in:

PLoS ONE, 2008, v. 3, n. 10, p. 1, doi. 10.1371/journal.pone.0003490

By:

Comabella, Manuel;
Craig, David W.;
Camiña-Tato, Montse;
Morcillo, Carlos;
Lopez, Cristina;
Navarro, Arcadi;
Rio, Jordi;
Montalban, Xavier;
Martin, Roland

Publication type:

Article

OUR HANDCUFFED POLICE: THE ASSAULT UPON LAW AND ORDER IN AMERICA AND WHAT CAN BE DONE ABOUT IT.

Published in:

1969

By:

Craig, David W.;
Gutterman, Melvin

Publication type:

Book Review

TO POLICE THE JUDGES--NOT JUST JUDGE THE POLICE.

Published in:

Journal of Criminal Law, Criminology & Police Science, 1966, v. 57, n. 3, p. 305, doi. 10.2307/1140727

By:

Craig, David W.

Publication type:

Article

Profiling the molecular and clinical landscape of glioblastoma utilizing the Oncology Research Information Exchange Network brain cancer database.

Published in:

Neuro-Oncology Advances, 2024, v. 6, n. 1, p. 1, doi. 10.1093/noajnl/vdae046

By:

Demetriou, Alexandra N;
Chow, Frances;
Craig, David W;
Webb, Michelle G;
Ormond, D Ryan;
Battiste, James;
Chakravarti, Arnab;
Colman, Howard;
Villano, John L;
Schneider, Bryan P;
Liu, James K C;
Churchman, Michelle L;
Zada, Gabriel

Publication type:

Article

Molecular Genetic Profiling of Adolescent Glassy Cell Carcinoma of the Cervix Reveals Targetable EGFR Amplification with Potential Therapeutic Implications.

Published in:

Journal of Adolescent & Young Adult Oncology, 2016, v. 5, n. 3, p. 297, doi. 10.1089/jayao.2015.0068

By:

McEachron, Troy A.;
Sender, Leonard S.;
Zabokrtsky, Keri B.;
Kaltenecker, Brian;
Holmes, W. Nathan;
Cherni, Irene;
Manojlovic, Zarko;
Liao, Shu-Yuan;
Craig, David W.;
Carpten, John D.;
Torno, Lilibeth R.

Publication type:

Article

In vitro-differentiated neural cell cultures progress towards donor-identical brain tissue.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 17, p. 3534, doi. 10.1093/hmg/ddt208

By:

Hjelm, Brooke E.;
Salhia, Bodour;
Kurdoglu, Ahmet;
Szelinger, Szabolcs;
Reiman, Rebecca A.;
Sue, Lucia I.;
Beach, Thomas G.;
Huentelman, Matthew J.;
Craig, David W.

Publication type:

Article

A Planner's Guide to Land Use Law (Book Review).

Published in:

1984

By:

Craig, David W.

Publication type:

Book Review

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

Using social norms to reduce bullying: A research intervention among adolescents in five middle schools.

Published in:

Group Processes & Intergroup Relations, 2011, v. 14, n. 5, p. 703, doi. 10.1177/1368430210398004

By:

Perkins, H. Wesley;
Craig, David W.;
Perkins, Jessica M.

Publication type:

Article

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

A prospective pilot study of genome-wide exome and transcriptome profiling in patients with small cell lung cancer progressing after first-line therapy.

Published in:

PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0179170

By:

Weiss, Glen J.;
Byron, Sara A.;
Aldrich, Jessica;
Sangal, Ashish;
Barilla, Heather;
Kiefer, Jeffrey A.;
Carpten, John D.;
Craig, David W.;
Whitsett, Timothy G.

Publication type:

Article

Cerebellar Telomere Length and Psychiatric Disorders.

Published in:

Behavior Genetics, 2010, v. 40, n. 2, p. 250, doi. 10.1007/s10519-010-9338-0

By:

Dandan Zhang;
Cheng, Lijun;
Craig, David W.;
Redman, Margot;
Chunyu Liu

Publication type:

Article

Preliminary analysis of copy number variation in the ADNI cohort

Published in:

2010

By:

Swaminathan, Shanker;
Kim, Sungeun;
Shen, Li;
Risacher, Shannon L.;
Foroud, Tatiana;
Pankratz, Nathan;
Potkin, Steven G.;
Huentelman, Matthew J.;
Craig, David W.;
Weiner, Michael W.;
Saykin, Andrew J.

Publication type:

Abstract

Genome-wide association study of CSF biomarkers amyloid beta 1-42, tau and tau phosphorylated at threonine 181 in the ADNI cohort

Published in:

2010

By:

Kim, Sungeun;
Swaminathan, Shanker;
Shen, Li;
Risacher, Shannon L.;
Nho, Kwangsik;
Foroud, Tatiana;
Shaw, Leslie M.;
Trojanowski, John Q.;
Potkin, Steven G.;
Huentelman, Matthew J.;
Craig, David W.;
DeChairo, Bryan M.;
Weiner, Michael W.;
Saykin, Andrew J.

Publication type:

Abstract

Preliminary analysis of copy number variation in the ADNI cohort

Published in:

2010

By:

Swaminathan, Shanker;
Kim, Sungeun;
Shen, Li;
Risacher, Shannon L.;
Foroud, Tatiana;
Pankratz, Nathan;
Potkin, Steven G.;
Huentelman, Matthew J.;
Craig, David W.;
Weiner, Michael W.;
Saykin, Andrew J.

Publication type:

Abstract

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

P3-163: Identification of a novel risk gene for progressive supranuclear palsy by a genome-wide scan of 500,288 SNPs

Published in:

2006

By:

Melquist, Stacey;
Huentelman, Matthew J.;
Craig, David W.;
Baker, Matt;
Crook, Richard;
Pearson, John V.;
Zisman, Victoria L.;
Gass, Jennifer;
Adamson, Jennifer;
Szelinger, Szabolcs;
Cournevaux, Jason J.;
Cannon, Ashley;
Coon, Keith D.;
Dickson, Dennis W.;
Stephan, Dietrich;
Hutton, Michael

Publication type:

Abstract

P3-163: Identification of a novel risk gene for progressive supranuclear palsy by a genome-wide scan of 500,288 SNPs

Published in:

2006

By:

Melquist, Stacey;
Huentelman, Matthew J.;
Craig, David W.;
Baker, Matt;
Crook, Richard;
Pearson, John V.;
Zisman, Victoria L.;
Gass, Jennifer;
Adamson, Jennifer;
Szelinger, Szabolcs;
Cournevaux, Jason J.;
Cannon, Ashley;
Coon, Keith D.;
Dickson, Dennis W.;
Stephan, Dietrich;
Hutton, Michael

Publication type:

Abstract

Assessing and managing risk when sharing aggregate genetic variant data.

Published in:

2011

By:

Craig, David W.;
Goor, Robert M.;
Wang, Zhenyuan;
Paschall, Justin;
Ostell, Jim;
Feolo, Michael;
Sherry, Stephen T.;
Manolio, Teri A.

Publication type:

Correction Notice

Assessing and managing risk when sharing aggregate genetic variant data.

Published in:

2011

By:

Craig, David W.;
Goor, Robert M.;
Wang, Zhenyuan;
Paschall, Justin;
Ostell, Jim;
Feolo, Michael;
Sherry, Stephen T.;
Manolio, Teri A.

Publication type:

review

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

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

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

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.;
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Frontiers in Immunology, 2020, v. 11, p. 1, doi. 10.3389/fimmu.2020.01475

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