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Shan Yang
Observed names:
S Yang,
S. Yang,
SHAN YANG,
Yang, Shan
Institutions:
Fudan University,
Huashan Hospital,
Xi'an Jiaotong University
Observed institutions:
University of California, San Francisco,
University of California, Santa Cruz,
Fudan University,
BioNano Genomics (United States),
Zhongshan Hospital,
Huashan Hospital,
Invitae (United States),
Weill Cornell Medicine,
Xi'an Jiaotong University
show all 9
ORCID:
0000-0002-0770-6511
Observed ORCID:
0000-0002-0770-6511
OpenAlex ID:
A5101630546
Prevalence of Germline Variants in Prostate Cancer and Implications for Current Genetic Testing Guidelines
2019
·
Piper Nicolosi
, Elisa Ledet
, et al.
·
JAMA Oncology
·
366
PDF
Underdiagnosis of Hereditary Breast Cancer: Are Genetic Testing Guidelines a Tool or an Obstacle?
2018
·
Peter D. Beitsch
, Pat W. Whitworth
, et al.
·
Journal of Clinical Oncology
·
362
Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment
2015
·
Andrea Desmond
, Allison W. Kurian
, et al.
·
JAMA Oncology
·
333
Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation
2017
·
Yuya Kobayashi
, Shan Yang
, et al.
·
Genome Medicine
·
232
PDF
A Systematic Comparison of Traditional and Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Genes in More Than 1000 Patients
2015
·
Stephen E. Lincoln
, Yuya Kobayashi
, et al.
·
Journal of Molecular Diagnostics
·
206
A framework for exhaustively mapping functional missense variants
2017
·
Jochen Weile
, Song Sun
, et al.
·
Molecular Systems Biology
·
199
PDF
Yield and Utility of Germline Testing Following Tumor Sequencing in Patients With Cancer
2020
·
Stephen E. Lincoln
, Robert L. Nussbaum
, et al.
·
JAMA Network Open
·
131
PDF
Sources of discordance among germ-line variant classifications in ClinVar
2017
·
Shan Yang
, Stephen E Lincoln
, et al.
·
Genetics in Medicine
·
114
PDF
Prevalence of pathogenic germline cancer risk variants in high-risk urothelial carcinoma
2019
·
Amin H. Nassar
, Sarah Abou Alaiwi
, et al.
·
Genetics in Medicine
·
97
PDF
Underdiagnosis of Hereditary Breast and Ovarian Cancer in Medicare Patients: Genetic Testing Criteria Miss the Mark
2018
·
Shan Yang
, Jennifer E. Axilbund
, et al.
·
Annals of Surgical Oncology
·
75
Shifting landscapes of human MTHFR missense-variant effects
2021
·
Jochen Weile
, Nishka Kishore
, et al.
·
The American Journal of Human Genetics
·
67
PDF
Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk
2017
·
Erin O’Leary
, Daniela Iacoboni
, et al.
·
Annals of Surgical Oncology
·
66
PDF
Consistency ofBRCA1andBRCA2Variant Classifications Among Clinical Diagnostic Laboratories
2017
·
Stephen E. Lincoln
, Shan Yang
, et al.
·
JCO Precision Oncology
·
46
Human genome meeting 2016
2016
·
GUSTO study group
, A. K. Srivastava
, et al.
·
Human Genomics
·
40
PDF
Inherited DNA-repair gene mutations in African American men with prostate cancer
2020
·
Oliver Sartor
, Shan Yang
, et al.
·
Oncotarget
·
26
PDF
Trans-ethnic variation in germline variants of patients with renal cell carcinoma
2021
·
Sarah Abou Alaiwi
, Amin H. Nassar
, et al.
·
Cell Reports
·
24
PDF
Clinical Implications of Pathogenic Germline Variants in Small Intestine Neuroendocrine Tumors (SI-NETs)
2021
·
Kimberly Perez
, Matthew H. Kulke
, et al.
·
JCO Precision Oncology
·
20
Unexpected actionable genetic variants revealed by multigene panel testing of patients with uterine cancer
2022
·
Brandie Heald
, Sara Mokhtary
, et al.
·
Gynecologic Oncology
·
17
PDF
Clinical Cohort Analysis of Germline EGFR T790M Demonstrates Penetrance Across Ethnicities and Races, Sexes, and Ages
2020
·
Darcy K. Berry
, Xia Wang
, et al.
·
JCO Precision Oncology
·
12
Underdiagnosis of Hereditary Colorectal Cancers Among Medicare Patients: Genetic Testing Criteria for Lynch Syndrome Miss the Mark
2021
·
Charles Muller
, Sarah M. Nielsen
, et al.
·
JCO Precision Oncology
·
11
Clinical Genetics Testing Laboratories Have a Remarkably Low Rate of Clinically Significant Discordance When Interpreting Variants in Hereditary Cancer Syndrome Genes
2017
·
Robert L. Nussbaum
, Shan Yang
, et al.
·
Journal of Clinical Oncology
·
10
Data Sharing and Reproducible Clinical Genetic Testing: Successes and Challenges
2016
·
SHAN YANG
, MELISSA CLINE
, et al.
·
Pacific Symposium on Biocomputing (PSB)
·
10
Clinical Impact of Pathogenic Variants in DNA Damage Repair Genes beyond BRCA1 and BRCA2 in Breast and Ovarian Cancer Patients
2022
·
Whitney Espinel
, Marjan Champine
, et al.
·
Cancers
·
7
PDF
Impact of genetic status on the survival outcomes of patients with clinical stage I non-small cell lung cancer with a radiological pure-solid appearance
2022
·
Ke Sun
, Meiling Li
, et al.
·
Lung Cancer
·
7
Equivocal Association of RAD51 Polymorphisms with Risk of Esophageal Squamous Cell Carcinoma in a Chinese Population
2014
·
Shu-Xiang Zhang
, Shan Yang
, et al.
·
Asian Pacific Journal of Cancer Prevention
·
7
PDF
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Works count:
67
Citation count:
2,527
H-index:
17
I10-index:
22
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