Transcriptome analysis provides critical answers to the “variants of uncertain significance” conundrum

por Postel, Mackenzie D., Culver, Julie O., Ricker, Charité, Craig, David W.
Publicado 2022

Multiomic sequencing of paired primary and metastatic small bowel carcinoids

por Postel, Mackenzie D., Darabi, Sourat, Howe, James R., Liang, Winnie S., Craig, David W., Demeure, Michael J.
Publicado 2023

Translating RNA sequencing into clinical diagnostics: opportunities and challenges

por Byron, Sara A., Van Keuren-Jensen, Kendall R., Engelthaler, David M., Carpten, John D., Craig, David W.
Publicado 2016

Identification of somatic mutations in cancer through Bayesian-based analysis of sequenced genome pairs

por Christoforides, Alexis, Carpten, John D, Weiss, Glen J, Demeure, Michael J, Von Hoff, Daniel D, Craig, David W
Publicado 2013

A gain-of-function mutation in the GRIK2 gene causes neurodevelopmental deficits

por Guzmán, Yomayra F., Ramsey, Keri, Stolz, Jacob R., Craig, David W., Huentelman, Mathew J., Narayanan, Vinodh, Swanson, Geoffrey T.
Publicado 2017

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

por Comabella, Manuel, Craig, David W., Camiña-Tato, Montse, Morcillo, Carlos, Lopez, Cristina, Navarro, Arcadi, Rio, Jordi, Montalban, Xavier, Martin, Roland
Publicado 2008

Small RNA Deep Sequencing Identifies a Unique miRNA Signature Released in Serum Exosomes in a Mouse Model of Sjögren's Syndrome

por Kakan, Shruti Singh, Janga, Srikanth R., Cooperman, Benjamin, Craig, David W., Edman, Maria C., Okamoto, Curtis T., Hamm-Alvarez, Sarah F.
Publicado 2020

Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in mice

por Nakajima, Kazuo, Miranda, Alannah, Craig, David W., Shekhtman, Tatyana, Kmoch, Stanislav, Bleyer, Anthony, Szelinger, Szabolcs, Kato, Tadafumi, Kelsoe, John R.
Publicado 2020

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

por Huentelman, Matthew J, Craig, David W, Shieh, Albert D, Corneveaux, Jason J, Hu-Lince, Diane, Pearson, John V, Stephan, Dietrich A
Publicado 2005

Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays

por Homer, Nils, Szelinger, Szabolcs, Redman, Margot, Duggan, David, Tembe, Waibhav, Muehling, Jill, Pearson, John V., Stephan, Dietrich A., Nelson, Stanley F., Craig, David W.
Publicado 2008

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

por Weiss, Glen J., Byron, Sara A., Aldrich, Jessica, Sangal, Ashish, Barilla, Heather, Kiefer, Jeffrey A., Carpten, John D., Craig, David W., Whitsett, Timothy G.
Publicado 2017

Long insert whole genome sequencing for copy number variant and translocation detection

por Liang, Winnie S., Aldrich, Jessica, Tembe, Waibhav, Kurdoglu, Ahmet, Cherni, Irene, Phillips, Lori, Reiman, Rebecca, Baker, Angela, Weiss, Glen J., Carpten, John D., Craig, David W.
Publicado 2014

Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations

por 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
Publicado 2022

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

por 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
Publicado 2005

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

por 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.
Publicado 2014

IDENTIFICATION OF GENETIC VARIANTS USING BARCODED MULTIPLEXED SEQUENCING

por Craig, David W., Pearson, John V., Szelinger, Szabolcs, Sekar, Aswin, Margot, Redma, Corneveaux, Jason J., Pawlowski, Traci L., Laub, Trisha, Nunn, Gary, Stephan, Dietrich A., Homer, Nils, Huentelman, Matthew J.
Publicado 2008

Open-access synthetic spike-in mRNA-seq data for cancer gene fusions

por Tembe, Waibhav D, Pond, Stephanie JK, Legendre, Christophe, Chuang, Han-Yu, Liang, Winnie S, Kim, Nancy E, Montel, Valerie, Wong, Shukmei, McDaniel, Timothy K, Craig, David W, Carpten, John D
Publicado 2014

Single-cell sequencing of genomic DNA resolves sub-clonal heterogeneity in a melanoma cell line

por Velazquez-Villarreal, Enrique I., Maheshwari, Shamoni, Sorenson, Jon, Fiddes, Ian T., Kumar, Vijay, Yin, Yifeng, Webb, Michelle G., Catalanotti, Claudia, Grigorova, Mira, Edwards, Paul A., Carpten, John D., Craig, David W.
Publicado 2020

Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder

por 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
Publicado 2013

Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study

por 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., The Alzheimer's Disease Neuroimaging Initiative (ADNI)
Publicado 2011