Zarina Yelskaya (Liying Zhang)

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 32

Top Topics

Intellectual Disability

Top Venues

Molecular genetics & genomic medicine

Breast cancer research and treatment

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Ciyu Yang, Maksym Misyura, Sarah Kane, Vikas Rai, Alicia Latham, Zarina Yelskaya
Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family. Molecular genetics & genomic medicine 11 (2) (2023)
Ciyu Yang, Maksym Misyura, Sarah Kane, Vikas Rai, Alicia Latham, Zarina Yelskaya
Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family. Molecular genetics & genomic medicine (2023)
Jordan C Cheng, Neeti Swarup, Feng Li, Misagh Kordi, Chien-Chung Lin, Szu-Chun Yang, Wei-Lun Huang, Mohammad Aziz, Yong Kim, David Chia, Yu-Min Yeh, Fang Wei, David Zheng, Zarina Yelskaya, Matteo Pellegrini, Wu-Chou Su, David T W Wong
Distinct Features of Plasma Ultrashort Single-Stranded Cell-Free DNA as Biomarkers for Lung Cancer Detection. Clinical chemistry (2023)
Ciyu Yang, Maksym Misyura, Sarah Kane, Vikas Rai, Alicia Latham, Zarina Yelskaya
Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family. Molecular genetics & genomic medicine (2023)
Ciyu Yang, Maksym Misyura, Sarah Kane, Vikas Rai, Alicia Latham, Zarina Yelskaya
Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family. Molecular genetics & genomic medicine 11 (2) (2023)
Ciyu Yang, Maksym Misyura, Sarah Kane, Vikas Rai, Alicia Latham, Zarina Yelskaya
Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family. Molecular genetics & genomic medicine (2023)
Ciyu Yang, Maksym Misyura, Sarah Kane, Vikas Rai, Alicia Latham, Zarina Yelskaya
Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family. Molecular genetics & genomic medicine 11 (2) (2023)
Ciyu Yang, Maksym Misyura, Sarah Kane, Vikas Rai, Alicia Latham, Zarina Yelskaya
Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family. Molecular genetics & genomic medicine 11 (2) (2023)
Blake Salfer, Feng Li, David T W Wong, Zarina Yelskaya
Urinary Cell-Free DNA in Liquid Biopsy and Cancer Management. Clinical chemistry 68 (12) (2022)
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Zarina Yelskaya, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam, null null
Optimising clinical care through CDH1 -specific germline variant curation: improvement of clinical assertions and updated curation guidelines. Journal of medical genetics (2022)
Eugene J Pietzak, Karissa A Whiting, Preethi Srinivasan, Chaitanya Bandlamudi, Aliya Khurram, Joseph Vijai, Aleksandra Walasek, Emily Bochner, Timothy N Clinton, Nima Almassi, Hong Truong, Manual De Jesus Escano, Michal Wiseman, Diana L Mandelker, Yelena M Kemel, Zarina Yelskaya, Michael F Walsh, Karen A Cadoo, Jonathan A Coleman, Hikmat A Al-Ahmadie, Jonathan E Rosenberg, Gopakumar V Iyer, David B Solit, Irina Ostrovnaya, Kenneth Offit, Mark E Robson, Zsofia K Stadler, Michael F Berger, Dean F Bajorin, Maria Isabel Carlo, Bernard H Bochner
Inherited Germline Cancer Susceptibility Gene Variants in Individuals with Non-Muscle-Invasive Bladder Cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 28 (19) (2022)
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Zarina Yelskaya, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam, null null
Optimising clinical care through CDH1 -specific germline variant curation: improvement of clinical assertions and updated curation guidelines. Journal of medical genetics (2022)
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Zarina Yelskaya, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam, null null
Optimising clinical care through CDH1 -specific germline variant curation: improvement of clinical assertions and updated curation guidelines. Journal of medical genetics (2022)
Chiyun Wang, Zarina Yelskaya, Efsevia Vakiani, Jinru Shia
Detecting mismatch repair deficiency in solid neoplasms: immunohistochemistry, microsatellite instability, or both? Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 35 (11) (2022)
Jennifer L Hay, Erica H Lee, Stephanie N Christian, Elizabeth Schofield, Jada G Hamilton, Ciyu Yang, Bobak Hedayati, Keimya Sadeghi, Mark E Robson, Allan C Halpern, Zarina Yelskaya, Irene Orlow
Interest and Utility of MC1R Testing for Melanoma Risk in Dermatology Patients with a History of Nonmelanoma Skin Cancer. Journal of skin cancer 2022 (2022)
Ciyu Yang, Yirong Li, Magan Trottier, Michael P Farrell, Vikas K Rai, Erin E Salo-Mullen, David J Gallagher, Zsofia K Stadler, Heleen M van der Klift, Zarina Yelskaya
Insertion of an SVA element in MSH2 as a novel cause of Lynch syndrome. Genes, chromosomes & cancer 60 (8) (2021)
Ciyu Yang, Angela G Arnold, Amanda Catchings, Vikas Rai, Zsofia K Stadler, Zarina Yelskaya
The RAD51D c.82G>A (p.Val28Met) variant disrupts normal splicing and is associated with hereditary ovarian cancer. Breast cancer research and treatment 185 (3) (2021)
Eric Lu, Kathryn E Hatchell, Sarah M Nielsen, Edward D Esplin, Karen Ouyang, Keith Nykamp, Shirin Zavoshi, Shantao Li, Zarina Yelskaya, Blake R Wilde, Heather R Christofk, Paul C Boutros, Brian M Shuch
Fumarate hydratase variant prevalence and manifestations among individuals receiving germline testing. Cancer (2021)
Christopher J Schwartz, Edaise M Da Silva, Antonio Marra, Andrea M Gazzo, Pier Selenica, Vikas K Rai, Diana Mandelker, Fresia Pareja, Maksym Misyura, Timothy M D'Alfonso, Edi Brogi, Pamela Drullinsky, Pedram Razavi, Mark E Robson, Joshua Z Drago, Hannah Y Wen, Zarina Yelskaya, Britta Weigelt, Jinru Shia, Jorge S Reis-Filho, Hong Zhang
Morphologic and Genomic Characteristics of Breast Cancers Occurring in Individuals with Lynch Syndrome. Clinical cancer research : an official journal of the American Association for Cancer Research (2021)
Ciyu Yang, Margaret Sheehan, Ester Borras, Karen Cadoo, Kenneth Offit, Zarina Yelskaya
Characterization of a germline splice site variant MLH1 c.678-3T>A in a Lynch syndrome family. Familial cancer 19 (4) (2021)
Zarina Yelskaya, Angela G Arnold, Vanessa J Marcell, Laura H Tang, Erin E Salo-Mullen, Vivian E Strong, Zsofia K Stadler, Zarina Yelskaya
Resolving pathogenicity classification for the CDH1 c.[715G>A] (p.Gly239Arg) Variant. European journal of human genetics : EJHG 29 (7) (2021)
Cristina Fortuno, Kristy Lee, Magali Olivier, Tina Pesaran, Phuong L Mai, Kelvin César de Andrade, Laura D Attardi, Stephanie Crowley, D Gareth Evans, Bing-Jian Feng, Ann K M Foreman, Megan N Frone, Robert Huether, Paul A James, Kelly McGoldrick, Jessica L Mester, Bryce A Seifert, Thomas P Slavin, Leora Witkowski, Zarina Yelskaya, Sharon E Plon, Amanda B Spurdle, Sharon A Savage, null null
Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants. Human mutation 42 (3) (2020)
Kelsey E Breen, Maria I Carlo, Yelena M Kemel, Anna Maio, Ying-Bei Chen, Zarina Yelskaya, Ozge Ceyhan-Birsoy, Diana Mandelker
Fumarate hydratase c.914T > C (p.Phe305Ser) is a pathogenic variant associated with hereditary leiomyomatosis and renal cell cancer syndrome. Molecular genetics & genomic medicine 8 (8) (2020)
Yirong Li, Erin Salo-Mullen, Anna Varghese, Magan Trottier, Zsofia K Stadler, Zarina Yelskaya
Insertion of an Alu-like element in MLH1 intron 7 as a novel cause of Lynch syndrome. Molecular genetics & genomic medicine 8 (12) (2020)
Yue Zhang, Jung-Young Park, Fan Zhang, Sara H Olson, Irene Orlow, Yirong Li, Robert C Kurtz, Marc Ladanyi, Jie Chen, Amanda Ewart Toland, Zarina Yelskaya, Paul R Andreassen
The p.Ser64Leu and p.Pro104Leu missense variants of PALB2 identified in familial pancreatic cancer patients compromise the DNA damage response. Human mutation 42 (2) (2020)
Zarina Yelskaya, Michael F Walsh, Sowmya Jairam, Diana Mandelker, Yi Zhong, Yelena Kemel, Ying-Bei Chen, David Musheyev, Ahmet Zehir, Gowtham Jayakumaran, Edyta Brzostowski, Ozge Birsoy, Ciyu Yang, Yirong Li, Joshua Somar, Deborah DeLair, Nisha Pradhan, Michael F Berger, Karen Cadoo, Maria I Carlo, Mark E Robson, Zsofia K Stadler, Christine A Iacobuzio-Donahue, Vijai Joseph, Kenneth Offit
Fumarate hydratase FH c.1431_1433dupAAA (p.Lys477dup) variant is not associated with cancer including renal cell carcinoma. Human mutation 41 (1) (2019)
Emiliano Cocco, Jamal Benhamida, Sumit Middha, Ahmet Zehir, Kerry Mullaney, Jinru Shia, Rona Yaeger, Zarina Yelskaya, Donna Wong, Liliana Villafania, Khedoudja Nafa, Maurizio Scaltriti, Alexander E Drilon, Leonard B Saltz, Alison M Schram, Zsofia K Stadler, David M Hyman, Ryma Benayed, Marc Ladanyi, Jaclyn F Hechtman
Colorectal Carcinomas Containing Hypermethylated MLH1 Promoter and Wild-Type BRAF/KRAS Are Enriched for Targetable Kinase Fusions. Cancer research 79 (6) (2019)
Ciyu Yang, Ozge Ceyhan-Birsoy, Diana Mandelker, Sowmya Jairam, Amanda Catchings, Eileen M O'Reilly, Michael F Walsh, Zarina Yelskaya
A synonymous germline variant PALB2 c.18G>T (p.Gly6=) disrupts normal splicing in a family with pancreatic and breast cancers. Breast cancer research and treatment 173 (1) (2018)
Diana Mandelker, Zarina Yelskaya
The emerging significance of secondary germline testing in cancer genomics. The Journal of pathology 244 (5) (2018)
Donavan T Cheng, Meera Prasad, Yvonne Chekaluk, Ryma Benayed, Justyna Sadowska, Ahmet Zehir, Aijazuddin Syed, Yan Elsa Wang, Joshua Somar, Yirong Li, Zarina Yelskaya, Donna Wong, Mark E Robson, Kenneth Offit, Michael F Berger, Khedoudja Nafa, Marc Ladanyi, Zarina Yelskaya
Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing. BMC medical genomics 10 (1) (2017)
Ciyu Yang, Sowmya Jairam, Kimberly A Amoroso, Mark E Robson, Michael F Walsh, Zarina Yelskaya
Characterization of a novel germline BRCA1 splice variant, c.5332+4delA. Breast cancer research and treatment 168 (2) (2017)
Zarina Yelskaya, Ruben Bacares, Erin Salo-Mullen, Joshua Somar, Deborah A Lehrich, Grace-Ann Fasaye, Daniel G Coit, Laura H Tang, Zsofia K Stadler, Liying Zhang
CDH1 Missense Variant c.1679C>G (p.T560R) Completely Disrupts Normal Splicing through Creation of a Novel 5' Splice Site. PloS one 11 (11) (2016)