Katherine L Nathanson


Ontology type: schema:Person     


Person Info

NAME

Katherine L

SURNAME

Nathanson

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-01 Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-12 CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing in GENOME BIOLOGY
  • 2018-10-04 Response to Hannah-Shmouni and Stratakis in GENETICS IN MEDICINE
  • 2018-07 Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) in GENETICS IN MEDICINE
  • 2018-04 Genetic variants demonstrating flip-flop phenomenon and breast cancer risk prediction among women of African ancestry in BREAST CANCER RESEARCH AND TREATMENT
  • 2018-03 Corrigendum: Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance in NATURE
  • 2017-12 The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk in NPJ BREAST CANCER
  • 2017-12 BRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers in NATURE COMMUNICATIONS
  • 2017-12 Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk in NPJ BREAST CANCER
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-07 Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor in NATURE GENETICS
  • 2017-06 Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance in NATURE
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-05 T-cell invigoration to tumour burden ratio associated with anti-PD-1 response in NATURE
  • 2017-04 Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-01 Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-12 Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women in BREAST CANCER RESEARCH
  • 2016-12 Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 in BREAST CANCER RESEARCH
  • 2016-12 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-10 Genetic variants in microRNA and microRNA biogenesis pathway genes and breast cancer risk among women of African ancestry in HUMAN GENETICS
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-09 Counselling framework for moderate-penetrance cancer-susceptibility mutations in NATURE REVIEWS CLINICAL ONCOLOGY
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-04 Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 in NATURE GENETICS
  • 2016-01 Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing in GENETICS IN MEDICINE
  • 2016 Genomic Biomarkers for Breast Cancer Risk in NOVEL BIOMARKERS IN THE CONTINUUM OF BREAST CANCER
  • 2015-12 An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2015-12 DCIS in BRCA1 and BRCA2 mutation carriers: prevalence, phenotype, and expression of oncodrivers C-MET and HER3 in JOURNAL OF TRANSLATIONAL MEDICINE
  • 2015-12 Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas in NATURE COMMUNICATIONS
  • 2015-12 MicroRNA expression profiling predicts clinical outcome of carboplatin/paclitaxel-based therapy in metastatic melanoma treated on the ECOG-ACRIN trial E2603 in CLINICAL EPIGENETICS
  • 2015-08 Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer in GENETICS IN MEDICINE
  • 2015-06 Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility in GENETICS IN MEDICINE
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 2015 Genomic Assessment of Renal Cancer in RENAL CELL CARCINOMA
  • 2015 Molecular Diagnostics and Tumor Mutational Analysis in BRAF TARGETS IN MELANOMA
  • 2015 Inherited and Somatic Genetics of Pancreatic Neuroendocrine Tumors in MANAGEMENT OF PANCREATIC NEUROENDOCRINE TUMORS
  • 2014-12 Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2014-11 Panel testing for inherited susceptibility to breast, ovarian, and colorectal cancer in GENETICS IN MEDICINE
  • 2014 Tissue Resources for Clinical Use and Marker Studies in Melanoma in MOLECULAR DIAGNOSTICS FOR MELANOMA
  • 2013-12 Common breast cancer risk variants in the post-COGS era: a comprehensive review in BREAST CANCER RESEARCH
  • 2013-12 Germ-line DICER1 mutations do not make a major contribution to the etiology of familial testicular germ cell tumours in BMC RESEARCH NOTES
  • 2013-10 A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia in NATURE GENETICS
  • 2013-09 Immunotherapy at Large: The road to personalized cancer vaccines in NATURE MEDICINE
  • 2013-06 A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry in NATURE GENETICS
  • 2013-06 COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration in BREAST CANCER RESEARCH
  • 2013-06 Meta-analysis identifies four new loci associated with testicular germ cell tumor in NATURE GENETICS
  • 2013-05 Inherited Mutations in Pheochromocytoma and Paraganglioma: Why All Patients Should Be Offered Genetic Testing in ANNALS OF SURGICAL ONCOLOGY
  • 2013-04 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer in NATURE GENETICS
  • 2013-01 A genome-wide association study of breast cancer in women of African ancestry in HUMAN GENETICS
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