|
| 36260525 | Gene Expression Profiling Identifies Two Chordoma Subtypes Associated with Distinct Molecular Mechanisms and Clinical Outcomes. | Clin Cancer Res | 2023 |
| 36260525 | Gene Expression Profiling Identifies Two Chordoma Subtypes Associated with Distinct Molecular Mechanisms and Clinical Outcomes. | Clin Cancer Res | 2023 |
| 37585199 | Estimated Prevalence, Tumor Spectrum, and Neurofibromatosis Type 1-Like Phenotype of CDKN2A-Related Melanoma-Astrocytoma Syndrome. | JAMA Dermatol | 2023 |
| 37213281 | Editorial: Chordoma: advances in biology and clinical management. | Front Oncol | 2023 |
| 36707629 | FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. | Eur J Hum Genet | 2023 |
| 37010652 | Tumour Infiltrating Lymphocytes (TILs) and immune composition in breast cancer patients from Kenya: Spatial distributions and associations with risk factors and tumour characteristics. | Breast Cancer Res Treat | 2023 |
| 36876055 | Association of germline variants in telomere maintenance genes (<i>POT1, TERF2IP, ACD,</i> and <i>TERT</i>) with spitzoid morphology in familial melanoma: A multi-center case series. | JAAD Int | 2023 |
| 37451831 | Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel. | J Med Genet | 2023 |
| 37444426 | Spectrum and Frequency of Germline <i>FANCM</i> Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases. | Cancers (Basel) | 2023 |
| 36991516 | DNA methylation age in paired tumor and adjacent normal breast tissue in Chinese women with breast cancer. | Clin Epigenetics | 2023 |
| 37585199 | Estimated Prevalence, Tumor Spectrum, and Neurofibromatosis Type 1-Like Phenotype of CDKN2A-Related Melanoma-Astrocytoma Syndrome. | JAMA Dermatol | 2023 |
| 36991516 | DNA methylation age in paired tumor and adjacent normal breast tissue in Chinese women with breast cancer. | Clin Epigenetics | 2023 |
| 37451831 | Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel. | J Med Genet | 2023 |
| 37213281 | Editorial: Chordoma: advances in biology and clinical management. | Front Oncol | 2023 |
| 37444426 | Spectrum and Frequency of Germline <i>FANCM</i> Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases. | Cancers (Basel) | 2023 |
| 37010652 | Tumour Infiltrating Lymphocytes (TILs) and immune composition in breast cancer patients from Kenya: Spatial distributions and associations with risk factors and tumour characteristics. | Breast Cancer Res Treat | 2023 |
| 36876055 | Association of germline variants in telomere maintenance genes (<i>POT1, TERF2IP, ACD,</i> and <i>TERT</i>) with spitzoid morphology in familial melanoma: A multi-center case series. | JAAD Int | 2023 |
| 36707629 | FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. | Eur J Hum Genet | 2023 |
| 34906508 | Novel loss-of-function variant in DENND5A impedes melanosomal cargo transport and predisposes to familial cutaneous melanoma. | Genet Med | 2022 |
| 35585550 | Breast cancer risks associated with missense variants in breast cancer susceptibility genes. | Genome Med | 2022 |
| 35762214 | Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma. | Hum Mutat | 2022 |
| 35377867 | SUITOR: Selecting the number of mutational signatures through cross-validation. | PLoS Comput Biol | 2022 |
| 36269225 | Impact of Transcript (p16/p14ARF) Alteration on Cancer Risk in CDKN2A Germline Pathogenic Variant Carriers. | JNCI Cancer Spectr | 2022 |
| 35723569 | Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes: Pooled Analysis of Population-Based Studies. | J Natl Cancer Inst | 2022 |
| 36409970 | Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in <i>CDKN2A</i> and Pancreatic Cancer. | JCO Precis Oncol | 2022 |
| 35717579 | Rare germline deleterious variants increase susceptibility for lung cancer. | Hum Mol Genet | 2022 |
| 35333343 | Association of Genetic Ancestry With Terminal Duct Lobular Unit Involution Among Healthy Women. | J Natl Cancer Inst | 2022 |
| 35042965 | Rare germline copy number variants (CNVs) and breast cancer risk. | Commun Biol | 2022 |
| 34906508 | Novel loss-of-function variant in DENND5A impedes melanosomal cargo transport and predisposes to familial cutaneous melanoma. | Genet Med | 2022 |
| 35181301 | Integrated Analysis of Coexpression and Exome Sequencing to Prioritize Susceptibility Genes for Familial Cutaneous Melanoma. | J Invest Dermatol | 2022 |
| 35585550 | Breast cancer risks associated with missense variants in breast cancer susceptibility genes. | Genome Med | 2022 |
| 35377867 | SUITOR: Selecting the number of mutational signatures through cross-validation. | PLoS Comput Biol | 2022 |
| 35762214 | Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma. | Hum Mutat | 2022 |
| 35723569 | Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes: Pooled Analysis of Population-Based Studies. | J Natl Cancer Inst | 2022 |
| 35717579 | Rare germline deleterious variants increase susceptibility for lung cancer. | Hum Mol Genet | 2022 |
| 36409970 | Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in <i>CDKN2A</i> and Pancreatic Cancer. | JCO Precis Oncol | 2022 |
| 36269225 | Impact of Transcript (p16/p14ARF) Alteration on Cancer Risk in CDKN2A Germline Pathogenic Variant Carriers. | JNCI Cancer Spectr | 2022 |
| 35042965 | Rare germline copy number variants (CNVs) and breast cancer risk. | Commun Biol | 2022 |
| 35181301 | Integrated Analysis of Coexpression and Exome Sequencing to Prioritize Susceptibility Genes for Familial Cutaneous Melanoma. | J Invest Dermatol | 2022 |
| 35333343 | Association of Genetic Ancestry With Terminal Duct Lobular Unit Involution Among Healthy Women. | J Natl Cancer Inst | 2022 |
| 32359158 | Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk. | J Natl Cancer Inst | 2021 |
| 32359158 | Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk. | J Natl Cancer Inst | 2021 |
| 33811164 | The Impact of Longitudinal Surveillance on Tumor Thickness for Melanoma-Prone Families with and without Pathogenic Germline Variants of <i>CDKN2A</i> and <i>CDK4</i>. | Cancer Epidemiol Biomarkers Prev | 2021 |
| 34174935 | Breast cancer risk factors in relation to molecular subtypes in breast cancer patients from Kenya. | Breast Cancer Res | 2021 |
| 34070849 | Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility. | Cancers (Basel) | 2021 |
| 33536423 | Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival. | Nat Commun | 2021 |
| 33471991 | Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women. | N Engl J Med | 2021 |
| 33952648 | Tumor-Associated Stromal Cellular Density as a Predictor of Recurrence and Mortality in Breast Cancer: Results from Ethnically Diverse Study Populations. | Cancer Epidemiol Biomarkers Prev | 2021 |
| 33990587 | Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers. | Nat Commun | 2021 |
| 33500318 | Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium. | Cancer Epidemiol Biomarkers Prev | 2021 |