John David Carpten


Ontology type: schema:Person     


Person Info

NAME

John David

SURNAME

Carpten

Publications in SciGraph latest 50 shown

  • 2022-04-06 Analysis of the genomic landscapes of Barbadian and Nigerian women with triple negative breast cancer in CANCER CAUSES & CONTROL
  • 2021-10-11 Correction: Comprehensive molecular profiling of UV-induced metastatic melanoma in Nme1/Nme2-deficient mice reveals novel markers of survival in human patients in ONCOGENE
  • 2021-08-25 Comprehensive molecular profiling of UV-induced metastatic melanoma in Nme1/Nme2-deficient mice reveals novel markers of survival in human patients in ONCOGENE
  • 2021-06-29 Making cancer research more inclusive in NATURE REVIEWS CANCER
  • 2021-02-12 Multiethnic PDX models predict a possible immune signature associated with TNBC of African ancestry in BREAST CANCER RESEARCH AND TREATMENT
  • 2021-01-20 Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction in NATURE GENETICS
  • 2021-01-04 Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction in NATURE GENETICS
  • 2020-06-25 Single-cell sequencing of genomic DNA resolves sub-clonal heterogeneity in a melanoma cell line in COMMUNICATIONS BIOLOGY
  • 2020-05-19 Developing a Novel Framework for an Undergraduate Cancer Research Education and Engagement Program for Underrepresented Minority Students: the Florida-California CaRE2 Research Education Core (REC) Training Program in JOURNAL OF CANCER EDUCATION
  • 2019-02-06 Comparison of TCGA and GENIE genomic datasets for the detection of clinically actionable alterations in breast cancer in SCIENTIFIC REPORTS
  • 2018-09-28 E6201, an intravenous MEK1 inhibitor, achieves an exceptional response in BRAF V600E-mutated metastatic malignant melanoma with brain metastases in INVESTIGATIONAL NEW DRUGS
  • 2017-10-19 A method to reduce ancestry related germline false positives in tumor only somatic variant calling in BMC MEDICAL GENOMICS
  • 2017-10-05 A multicenter, randomized study of decitabine as epigenetic priming with induction chemotherapy in children with AML in CLINICAL EPIGENETICS
  • 2017-01-12 Identifying aggressive prostate cancer foci using a DNA methylation classifier in GENOME BIOLOGY
  • 2017-01-05 Case report: whole exome sequencing of primary cardiac angiosarcoma highlights potential for targeted therapies in BMC CANCER
  • 2016-12-23 Clinical Implementation of Integrated Genomic Profiling in Patients with Advanced Cancers in SCIENTIFIC REPORTS
  • 2016-04-20 A somatic reference standard for cancer genome sequencing in SCIENTIFIC REPORTS
  • 2016-04-07 Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation in NATURE COMMUNICATIONS
  • 2016-03-21 Translating RNA sequencing into clinical diagnostics: opportunities and challenges in NATURE REVIEWS GENETICS
  • 2014-12-19 Phase I study of the novel Cdc2/CDK1 and AKT inhibitor terameprocol in patients with advanced leukemias in INVESTIGATIONAL NEW DRUGS
  • 2014-09-30 Open-access synthetic spike-in mRNA-seq data for cancer gene fusions in BMC GENOMICS
  • 2014-09-14 A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer in NATURE GENETICS
  • 2014-06-18 Whole genome sequencing reveals potential targets for therapy in patients with refractory KRASmutated metastatic colorectal cancer in BMC MEDICAL GENOMICS
  • 2014-03-15 Whole-genome Sequencing of an Aggressive BRAF Wild-type Papillary Thyroid Cancer Identified EML4–ALK Translocation as a Therapeutic Target in WORLD JOURNAL OF SURGERY
  • 2013-10-26 Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease in HUMAN GENETICS
  • 2013-05-29 Expression and phosphorylation of the AS160_v2 splice variant supports GLUT4 activation and the Warburg effect in multiple myeloma in CANCER & METABOLISM
  • 2013-05-04 Identification of somatic mutations in cancer through Bayesian-based analysis of sequenced genome pairs in BMC GENOMICS
  • 2013-04-14 A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry in NATURE GENETICS
  • 2012-10-12 HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG) in HUMAN GENETICS
  • 2012-10-01 Interrogating of cancer genomes: towards more profile-based therapeutics in BMC PROCEEDINGS
  • 2012-08-05 Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer in FAMILIAL CANCER
  • 2012-07-04 Cancer of the ampulla of Vater: analysis of the whole genome sequence exposes a potential therapeutic vulnerability in GENOME MEDICINE
  • 2012-06-19 Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families in BMC MEDICAL GENOMICS
  • 2011-09-30 Molecular subtype analysis determines the association of advanced breast cancer in Egypt with favorable biology in BMC WOMEN'S HEALTH
  • 2011-05-22 Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21 in NATURE GENETICS
  • 2010-03-11 Correlation between array-comparative genomic hybridization-defined genomic gains and losses and survival: identification of 1p31-32 deletion as a prognostic factor in myeloma in LEUKEMIA
  • 2008-08-31 Evidence for two independent prostate cancer risk–associated loci in the HNF1B gene at 17q12 in NATURE GENETICS
  • 2008-01-01 Inherited Genetic Changes in Prostate Cancer in PROSTATE CANCER
  • 2007-07-04 A transforming mutation in the pleckstrin homology domain of AKT1 in cancer in NATURE
  • 2006-11-21 Fine-mapping the putative chromosome 17q21–22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis in HUMAN GENETICS
  • 2005-10-22 A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region in HUMAN GENETICS
  • 2005-05-20 A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region in HUMAN GENETICS
  • 2004-08-08 Nonsense-mediated decay microarray analysis identifies mutations of EPHB2 in human prostate cancer in NATURE GENETICS
  • 2004-06-01 Clinical characteristics of African-American men with hereditary prostate cancer: the AAHPC study in PROSTATE CANCER AND PROSTATIC DISEASES
  • 2002-11-18 HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome in NATURE GENETICS
  • 2002-11-04 RNASEL Arg462Gln variant is implicated in up to 13% of prostate cancer cases in NATURE GENETICS
  • 2002-09-16 Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk in NATURE GENETICS
  • 2002-01-23 Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk in HUMAN GENETICS
  • 2002-01-22 Germline mutations in the ribonuclease L gene in families showing linkage with HPC1 in NATURE GENETICS
  • 2002-01-01 Prostate cancer susceptibility genes: Many studies, many results, no answers in PROSTATE CANCER: NEW HORIZONS IN RESEARCH AND TREATMENT
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