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Chun-Ling Hu · SciRah

Researcher profile · Semantic Scholar

Chun-Ling Hu

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Chun-Ling Hu — researcher profile on SciRah

h-index: 40
Works: 129
Citations: 6,066

Most-cited papers

A Population-Based Study of Genes Previously Implicated in Breast Cancer
Chun-Ling Hu, S. Hart, Rohan D. Gnanaolivu, Hong-Yan Huang +56 more
2021New England Journal of Medicine695 citations Open access
Semantic Scholar
Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer
F. Couch, H. Shimelis, Chun-Ling Hu, S. Hart +14 more
2017JAMA Oncology580 citations Open access
Semantic Scholar
Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer
Chun-Ling Hu, S. Hart, E. Polley, Rohan D. Gnanaolivu +15 more
2018Journal of the American Medical Association (JAMA)509 citations Open access
Semantic Scholar
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
R. Milne, Karoline B. Kuchenbaecker, K. Michailidou, J. Beesley +466 more
2017Nature Genetics379 citations Open access
Semantic Scholar
Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing
H. Shimelis, H. LaDuca, Chun-Ling Hu, S. Hart +25 more
2018Journal of the National Cancer Institute291 citations Open access
Semantic Scholar
A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients
H. LaDuca, E. Polley, Amal Yussuf, Lily Hoang +17 more
2019Genetics in Medicine197 citations Open access
Semantic Scholar
Contralateral Breast Cancer Risk Among Carriers of Germline Pathogenic Variants in ATM, BRCA1, BRCA2, CHEK2, and PALB2
S. Yadav, N. Boddicker, Jie Na, E. Polley +32 more
2023Journal of Clinical Oncology144 citations Open access
Semantic Scholar
The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk
T. Slavin, Kara N. Maxwell, J. Lilyquist, J. Vijai +23 more
2017npj Breast Cancer138 citations Open access
Semantic Scholar
Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls
J. Lilyquist, H. LaDuca, E. Polley, Brigette Tippin Davis +6 more
2017Gynecologic Oncology134 citations Open access
Semantic Scholar
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
Kara N. Maxwell, S. Hart, J. Vijai, K. Schrader +16 more
2016American Journal of Human Genetics123 citations Open access
Semantic Scholar
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
D. Barnes, M. Rookus, L. McGuffog, Goska Leslie +190 more
2020Genetics in Medicine116 citations Open access
Semantic Scholar
The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort
Chun-Ling Hu, E. Polley, S. Yadav, J. Lilyquist +9 more
2020Journal of the National Cancer Institute103 citations Open access
Semantic Scholar
BRCA1/2 Mutations and Bevacizumab in the Neoadjuvant Treatment of Breast Cancer: Response and Prognosis Results in Patients With Triple-Negative Breast Cancer From the GeparQuinto Study
P. Fasching, S. Loibl, Chun-Ling Hu, S. Hart +23 more
2018Journal of Clinical Oncology100 citations Open access
Semantic Scholar
Evaluation of Germline Genetic Testing Criteria in a Hospital-Based Series of Women With Breast Cancer
S. Yadav, Chun-Ling Hu, S. Hart, N. Boddicker +23 more
2020Journal of Clinical Oncology92 citations Open access
Semantic Scholar
Guidelines an
S. Hart, E. Polley, Amal Yussuf, S. Yadav +9 more
201991 citations
Semantic Scholar
Breast Cancer Screening Strategies for Women With ATM, CHEK2, and PALB2 Pathogenic Variants: A Comparative Modeling Analysis.
K. Lowry, H. A. Geuzinge, Natasha K. Stout, O. Alagoz +19 more
2022JAMA Oncology84 citations Open access
Semantic Scholar
BRCA2 hypomorphic missense variants confer moderate risks of breast cancer
H. Shimelis, Romy L. S. Mesman, C. von Nicolai, Åsa Ehlén +130 more
2017Cancer Research84 citations Open access
Semantic Scholar
Mapping molecular subtype specific alterations in breast cancer brain metastases identifies clinically relevant vulnerabilities
Nicola Cosgrove, D. Varešlija, S. Keelan, Ashuvinee Elangovan +15 more
2022Nature Communications80 citations Open access
Semantic Scholar
Contribution of Germline Predisposition Gene Mutations to Breast Cancer Risk in African American Women.
J. Palmer, E. Polley, Chun-Ling Hu, E. John +28 more
2020Journal of the National Cancer Institute77 citations Open access
Semantic Scholar
Risk of Breast Cancer Among Carriers of Pathogenic Variants in Breast Cancer Predisposition Genes Varies by Polygenic Risk Score
Chi Gao, E. Polley, S. Hart, Hong-Yan Huang +38 more
2021Journal of Clinical Oncology76 citations Open access
Semantic Scholar
Mutations in BRCA1/2 and Other Panel Genes in Patients With Metastatic Breast Cancer —Association With Patient and Disease Characteristics and Effect on Prognosis
P. Fasching, S. Yadav, Chun-Ling Hu, M. Wunderle +33 more
2021Journal of Clinical Oncology76 citations Open access
Semantic Scholar
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
L. Guidugli, H. Shimelis, David L. Masica, V. Pankratz +9 more
2018American Journal of Human Genetics72 citations Open access
Semantic Scholar
Transcriptional induction of Periostin by a Sulfatase 2-TGFβ1-SMAD signaling axis mediates tumor angiogenesis in hepatocellular carcinoma
Gang Chen, I. Nakamura, R. Dhanasekaran, E. Iguchi +26 more
2016Cancer Research62 citations Open access
Semantic Scholar
Multigene Hereditary Cancer Panels Reveal High-Risk Pancreatic Cancer Susceptibility Genes
Chun-Ling Hu, H. LaDuca, H. Shimelis, E. Polley +11 more
2018JCO Precision Oncology55 citations Open access
Semantic Scholar
Functional characterization of 84 PALB2 variants of uncertain significance
T. Wiltshire, Mandy Ducy, T. Foo, Chun-Ling Hu +10 more
2019Genetics in Medicine49 citations Open access
Semantic Scholar
Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast
S. Yadav, Chun-Ling Hu, K. Nathanson, J. Weitzel +38 more
2021Journal of Clinical Oncology47 citations Open access
Semantic Scholar
Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort
Hong-Yan Li, H. LaDuca, T. Pesaran, Elizabeth C. Chao +9 more
2019Genetics in Medicine45 citations Open access
Semantic Scholar
Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance
Marcy E. Richardson, Chun-Ling Hu, Kun Y. Lee, H. LaDuca +11 more
2021American Journal of Human Genetics44 citations Open access
Semantic Scholar
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
G. Figlioli, M. Bogliolo, Irene Catucci, Laura Caleca +473 more
2019npj Breast Cancer41 citations Open access
Semantic Scholar
Effect of germline mutations in homologous recombination repair genes on overall survival of patients with pancreatic adenocarcinoma
S. Yadav, P. Kasi, W. Bamlet, T. Ho +11 more
2020Clinical Cancer Research40 citations Open access
Semantic Scholar
Pathogenic Variants in Cancer Predisposition Genes and Prostate Cancer Risk in Men of African Ancestry
M. Matejcic, Yesha M. Patel, J. Lilyquist, Chun-Ling Hu +23 more
2020JCO Precision Oncology40 citations Open access
Semantic Scholar
Cancer susceptibility gene mutations in type I and II endometrial cancer
B. Long, J. Lilyquist, A. Weaver, Chun-Ling Hu +7 more
2018Gynecologic Oncology40 citations Open access
Semantic Scholar
Comparison of the Prevalence of Pathogenic Variants in Cancer Susceptibility Genes in Black Women and Non-Hispanic White Women With Breast Cancer in the United States.
S. Domchek, S. Yao, Fei Chen, Chun-Ling Hu +8 more
2021JAMA Oncology37 citations Open access
Semantic Scholar
Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer
S. Yadav, H. LaDuca, E. Polley, Chun-Ling Hu +14 more
2020Journal of the National Cancer Institute36 citations Open access
Semantic Scholar
Mutation prevalence tables for hereditary cancer derived from multi-gene panel testing
S. Hart, E. Polley, Amal Yussuf, S. Yadav +8 more
2019Human Mutation32 citations Open access
Semantic Scholar
Risk of Late-Onset Breast Cancer in Genetically Predisposed Women
N. Boddicker, Chun-Ling Hu, J. Weitzel, P. Kraft +47 more
2021Journal of Clinical Oncology30 citations Open access
Semantic Scholar
Long Noncoding RNA HOTTIP Promotes Mouse Hepatic Stellate Cell Activation via Downregulating miR-148a
Zhi-Qin Li, Jia Wang, Qing-Lei Zeng, Chun-Ling Hu +5 more
2018Cellular Physiology and Biochemistry27 citations Open access
Semantic Scholar
Contribution of Inherited DNA-Repair Gene Mutations to Hormone-Sensitive and Castrate-Resistant Metastatic Prostate Cancer and Implications for Clinical Outcome.
S. Yadav, S. Hart, Chun-Ling Hu, D. Hillman +6 more
2019JCO Precision Oncology21 citations Open access
Semantic Scholar
The development of hepatocarcinoma after long-term antivirus treatment of Chinese patients with chronic hepatitis B virus infection: Incidence, long-term outcomes and predictive factors.
Zhi-Qin Li, Chun-Ling Hu, Ping Yu, Xin-yu Gu +9 more
2017Clinics And Research in Hepatology and Gastroenterology21 citations
Semantic Scholar
Abstract PD1-02: Cancer predisposition genes in metastatic breast cancer – Association with metastatic pattern, prognosis, patient and tumor characteristics
P. Fasching, Chun-Ling Hu, S. Hart, E. Polley +25 more
201820 citations
Semantic Scholar
Classification of BRCA2 variants of uncertain significance (VUS) using an ACMG/AMP model incorporating a homology directed repair (HDR) functional assay
Chun-Ling Hu, Lisa R. Susswein, Maegan E. Roberts, Han Yang +15 more
2022Clinical Cancer Research17 citations Open access
Semantic Scholar
Functional analysis and clinical classification of 462 germline BRCA2 missense variants affecting the DNA binding domain.
Chun-Ling Hu, Huai-Zhi Huang, Jie Na, Carolyn A Lumby +22 more
2024American Journal of Human Genetics15 citations Open access
Semantic Scholar
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk
Lenka Stolařová, P. Kleiblová, P. Zemánková, Barbora Stastna +106 more
2023Clinical Cancer Research15 citations Open access
Semantic Scholar
Risk of Different Cancers Among First-degree Relatives of Pancreatic Cancer Patients: Influence of Probands’ Susceptibility Gene Mutation Status
S. Antwi, Sarah E Fagan, K. G. Chaffee, W. Bamlet +10 more
2018Journal of the National Cancer Institute15 citations Open access
Semantic Scholar
Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C
Chun-Ling Hu, Anil Belur Nagaraj, H. Shimelis, G. Montalban +40 more
2023Cancer Research14 citations Open access
Semantic Scholar
Genetic Risk of Second Primary Cancer in Breast Cancer Survivors: The Multiethnic Cohort Study
Fei Chen, Sungshim L. Park, L. Wilkens, Peggy C. Wan +7 more
2022Cancer Research14 citations Open access
Semantic Scholar
Decreased Expression of Sulfatase 2 in the Brains of Alzheimer’s Disease Patients: Implications for Regulation of Neuronal Cell Signaling
R. Roberts, Yoo Na N Kang, Chun-Ling Hu, Catherine D. Moser +6 more
2017Journal of Alzheimer's disease reports14 citations Open access
Semantic Scholar
Knockout of Sulfatase 2 is associated with decreased steatohepatitis and fibrosis in a mouse model of nonalcoholic fatty liver disease.
Tae Hyo Kim, B. Banini, Faizal Z. Asumda, Nellie A Campbell +12 more
2020American Journal of Physiology - Gastrointestinal and Liver Physiology13 citations Open access
Semantic Scholar
Mutation Rates in Cancer Susceptibility Genes in Patients With Breast Cancer With Multiple Primary Cancers.
Kara N. Maxwell, Brandon M. Wenz, Abha Kulkarni, B. Wubbenhorst +25 more
2020JCO Precision Oncology11 citations Open access
Semantic Scholar
CRM1 inhibitor anti-tumor activity is enhanced with salicylates by S-phase arrest and impaired DNA-damage repair.
J. Abeykoon, Xiao-Sheng Wu, K. Nowakowski, S. Dasari +26 more
2020Blood10 citations Open access
Semantic Scholar

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