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Author Details

David W Craig
University of Southern California
2004
152
58
PMIDPaper TitleJournal TitlePublished Year
36991131Focal adhesion is associated with lithium response in bipolar disorder: evidence from a network-based multi-omics analysis.Mol Psychiatry2024
37408271Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders.Cells2023
37954063Multiomic sequencing of paired primary and metastatic small bowel carcinoids.F1000Res2023
34437759Multi-omic molecular profiling guide's efficacious treatment selection in refractory metastatic breast cancer: a prospective phase II clinical trial.Mol Oncol2022
35546635Rare variants implicate NMDA receptor signaling and cerebellar gene networks in risk for bipolar disorder.Mol Psychiatry2022
35385219High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defects.Am J Med Genet A2022
34994087Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations.Mol Genet Genomic Med2022
34635800Correction: Comprehensive molecular profiling of UV-induced metastatic melanoma in Nme1/Nme2-deficient mice reveals novel markers of survival in human patients.Oncogene2021
33576900Multiethnic PDX models predict a possible immune signature associated with TNBC of African ancestry.Breast Cancer Res Treat2021
33826920Applicability of spatial transcriptional profiling to cancer research.Mol Cell2021
33826614Identifying treatment options for BRAFV600 wild-type metastatic melanoma: A SU2C/MRA genomics-enabled clinical trial.PLoS One2021
35024611Anatomical and topographical variations in the distribution of brain metastases based on primary cancer origin and molecular subtypes: a systematic review.Neurooncol Adv2021
35048876Characterisation of age and polarity at onset in bipolar disorder.Br J Psychiatry2021
34433909Comprehensive molecular profiling of UV-induced metastatic melanoma in Nme1/Nme2-deficient mice reveals novel markers of survival in human patients.Oncogene2021
32754643Congenital myasthenic syndrome caused by a frameshift insertion mutation in <i>GFPT1</i>.Neurol Genet2020
33235206Ntrk1 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.Transl Psychiatry2020
32743548Temporospatial genomic profiling in glioblastoma identifies commonly altered core pathways underlying tumor progression.Neurooncol Adv2020
32587328Single-cell sequencing of genomic DNA resolves sub-clonal heterogeneity in a melanoma cell line.Commun Biol2020
30503783Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.Eur Neuropsychopharmacol2019
31748968Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD).Hum Genet2019
30487653Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder.Neuropsychopharmacology2019
30264293E6201, an intravenous MEK1 inhibitor, achieves an exceptional response in BRAF V600E-mutated metastatic malignant melanoma with brain metastases.Invest New Drugs2019
29074604Prospective Feasibility Trial for Genomics-Informed Treatment in Recurrent and Progressive Glioblastoma.Clin Cancer Res2018
32714589A novel variant in <i>TAF1</i> affects gene expression and is associated with X-linked <i>TAF1</i> intellectual disability syndrome.Neuronal Signal2018
30160831A 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.Am J Med Genet A2018
29961512Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results.Semin Pediatr Neurol2018
30415424Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.Int J Bipolar Disord2018
29691419Author Correction: A population-specific reference panel empowers genetic studies of Anabaptist populations.Sci Rep2018
28056866Case report: whole exome sequencing of primary cardiac angiosarcoma highlights potential for targeted therapies.BMC Cancer2017
28139025A de novo splice site mutation in CASK causes FG syndrome-4 and congenital nystagmus.Am J Med Genet A2017
28373299Integrated genomic analyses reveal frequent <i>TERT</i> aberrations in acral melanoma.Genome Res2017
28446508Enrichment of PI3K-AKT-mTOR Pathway Activation in Hepatic Metastases from Breast Cancer.Clin Cancer Res2017
28180184A gain-of-function mutation in the <i>GRIK2</i> gene causes neurodevelopmental deficits.Neurol Genet2017
28967789Exploring genome-wide DNA methylation patterns in Aicardi syndrome.Epigenomics2017
29052513A method to reduce ancestry related germline false positives in tumor only somatic variant calling.BMC Med Genomics2017
29166413Comprehensive molecular profiling of 718 Multiple Myelomas reveals significant differences in mutation frequencies between African and European descent cases.PLoS Genet2017
28729679A population-specific reference panel empowers genetic studies of Anabaptist populations.Sci Rep2017
28663785Case Report: Novel mutations in <i>TBC1D24</i> are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disability.F1000Res2017
28586388A prospective pilot study of genome-wide exome and transcriptome profiling in patients with small cell lung cancer progressing after first-line therapy.PLoS One2017
28057415Comprehensive Genomic Analysis of Metastatic Mucinous Urethral Adenocarcinoma Guides Precision Oncology Treatment: Targetable EGFR Amplification Leading to Successful Treatment With Erlotinib.Clin Genitourin Cancer2017
26996076Translating RNA sequencing into clinical diagnostics: opportunities and challenges.Nat Rev Genet2016
28003660Clinical Implementation of Integrated Genomic Profiling in Patients with Advanced Cancers.Sci Rep2016
27626064A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia.Cold Spring Harb Mol Case Stud2016
27653636Dystonia in ATP2B3-associated X-linked spinocerebellar ataxia.Mov Disord2016
27150464The Pharmacogenomics of Bipolar Disorder study (PGBD): identification of genes for lithium response in a prospective sample.BMC Psychiatry2016
27329760Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.Hum Mol Genet2016
27094764A somatic reference standard for cancer genome sequencing.Sci Rep2016
26974246Molecular Genetic Profiling of Adolescent Glassy Cell Carcinoma of the Cervix Reveals Targetable EGFR Amplification with Potential Therapeutic Implications.J Adolesc Young Adult Oncol2016
26727971Successful Treatment of Genetically Profiled Pediatric Extranodal NK/T-Cell Lymphoma Targeting Oncogenic STAT3 Mutation.Pediatr Blood Cancer2016
25592568An integrated framework for reporting clinically relevant biomarkers from paired tumor/normal genomic and transcriptomic sequencing data in support of clinical trials in personalized medicine.Pac Symp Biocomput2015
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Collaborators

Matthew J Huentelman
The Translational Genomics Research Institute (TGen)
Co-authored papers 49
John D Carpten
Co-authored papers 46
Szabolcs Szelinger
College of American Pathologists
Co-authored papers 40
Winnie S Liang
Co-authored papers 28
John V Pearson
QIMR Berghofer Medical Research Institute
Co-authored papers 21
Elliot S Gershon
University of Chicago
Co-authored papers 19
John R Kelsoe
University of California
Co-authored papers 18
Tatiana Foroud
Indiana University School of Medicine
Co-authored papers 18
John I Nurnberger
Stark Neurosciences Research Institute, Indiana University School of Medicine
Co-authored papers 16
Peter P Zandi
Johns Hopkins University School of Medicine
Co-authored papers 15
Melvin G McInnis
University of Michigan ann arbor
Co-authored papers 14
Angela Baker
Co-authored papers 14
William Coryell
University of Iowa
Co-authored papers 14
Wade H Berrettini
University of Pennsylvania
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Howard J Edenberg
Indiana University School of Medicine
Co-authored papers 13
Daniel D Von Hoff
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Caroline M Nievergelt
VA San Diego Healthcare System (VASDHS)
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Chunyu Liu
Boston University School of Public Health
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Judith A Badner
Rush University Medical College
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Nicholas J Schork
University of California San Diego
Co-authored papers 13
Eric M Reiman
Banner Alzheimer's Institute
Co-authored papers 12
Francis J McMahon
National Institute of Mental Health, National Institutes of Health
Co-authored papers 12
Paul D Shilling
University of California
Co-authored papers 11
Thomas G Schulze
SUNY Upstate Medical University
Co-authored papers 11
William A Scheftner
Rush Medical College
Co-authored papers 11
William B Lawson
Howard University
Co-authored papers 11
William Byerley
University of California san francisco
Co-authored papers 11
James B Potash
University Hospital Frankfurt
Co-authored papers 11
Evaristus Nwulia
Howard University Hospital
Co-authored papers 10
Maria Hipolito
Howard University Hospital
Co-authored papers 10
Release 1.2