human | Q5 |
P496 | ORCID iD | 0000-0003-4516-7421 |
P1153 | Scopus author ID | 55357578600 |
P69 | educated at | University of Cambridge | Q35794 |
St. Olaf College | Q1515763 | ||
Brigham and Women's Hospital | Q2900977 | ||
Medical College of Wisconsin | Q6806307 | ||
P108 | employer | National Institutes of Health | Q390551 |
Howard Hughes Medical Institute | Q1512226 | ||
Brigham and Women's Hospital | Q2900977 | ||
Medical College of Wisconsin | Q6806307 | ||
Foundation Medicine | Q19604401 | ||
P734 | family name | Decker | Q2674262 |
Decker | Q2674262 | ||
Decker | Q2674262 | ||
P106 | occupation | researcher | Q1650915 |
Q34650013 | A copy number variant at the KITLG locus likely confers risk for canine squamous cell carcinoma of the digit |
Q36891144 | Biallelic BRCA2 Mutations Shape the Somatic Mutational Landscape of Aggressive Prostate Tumors |
Q100440164 | CDKN2C-Null Leiomyosarcoma: A Novel, Genomically Distinct Class of TP53/RB1-Wild-Type Tumor With Frequent CIC Genomic Alterations and 1p/19q-Codeletion |
Q92005489 | Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families |
Q34044594 | Comparison against 186 canid whole-genome sequences reveals survival strategies of an ancient clonally transmissible canine tumor |
Q58546894 | Differential Burden of Rare and Common Variants on Tumor Characteristics, Survival, and Mode of Detection in Breast Cancer |
Q34147903 | Dysregulation of the homeobox transcription factor gene HOXB13: role in prostate cancer |
Q35752069 | Homologous Mutation to Human BRAF V600E Is Common in Naturally Occurring Canine Bladder Cancer--Evidence for a Relevant Model System and Urine-Based Diagnostic Test |
Q47586106 | Inherited mutations in BRCA1 and BRCA2 in an unselected multiethnic cohort of Asian patients with breast cancer and healthy controls from Malaysia |
Q28301461 | Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease |
Q37079859 | No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing |
Q92610736 | Peptide-TLR-7/8a conjugate vaccines chemically programmed for nanoparticle self-assembly enhance CD8 T-cell immunity to tumor antigens |
Q80666252 | Periodically arranged interactions within the myosin filament backbone revealed by mechanical unzipping |
Q91435452 | Prediction of DNA Repair Inhibitor Response in Short-Term Patient-Derived Ovarian Cancer Organoids |
Q62583372 | Prevalence of BRCA1 and BRCA2 pathogenic variants in a large, unselected breast cancer cohort |
Q40094101 | Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks |
Q91044035 | Targeted Resequencing of the Coding Sequence of 38 Genes Near Breast Cancer GWAS Loci in a Large Case-Control Study |
Q88605355 | Topology of interaction between titin and myosin thick filaments |
Q28728624 | Variation of BMP3 contributes to dog breed skull diversity |
Q37686900 | Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes |
Q64086417 | Whole genome sequencing of canids reveals genomic regions under selection and variants influencing morphology |
Search more.