Tom Walsh (T Walsh)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 7

Top Topics

Dna Methylation

Top Venues

Journal of medical genetics

Genome research

Proceedings of the National Academy of Sciences of the United States of America

Science (New York, N.Y.)

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

Publications

Suleyman Gulsuner, Amal AbuRayyan, Jessica B Mandell, Ming K Lee, Greta V Bernier, Barbara S Norquist, Sarah B Pierce, Mary-Claire King, Tom Walsh
Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumor-suppressor genes. Genome research (2024)
Tal Freund, Sarah K Baxter, Tom Walsh, Hana Golan, Joseph Kapelushnik, Michal Abramsohn-Goldenberg, Shira Benor, Nadav Sarid, Ron Ram, Yifat Alcalay, Reeval Segel, Paul Renbaum, Polina Stepensky, Mary-Claire King, Troy R Torgerson, David Hagin
Clinically Complex LRBA Deficiency Due to a Founder Allele in the Georgian Jewish Population. Journal of clinical immunology (2022)
Michal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, Aviva Fattal, Adi Aran, Alla Kuzminsky, Liora Sagi, Dafna Guttman, Nira Schneebaum Sender, Varda Gross-Tsur, Tehila Klopstock, Tom Walsh, Paul Renbaum, Sharon Zeligson, Lilach Shemer Meiri, Dorit Lev, Dorit Shmueli, Luba Blumkin, Amnon Lahad, Mary-Claire King, Ephrat Lahad Levy, Reeval Segel
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy. Journal of medical genetics (2021)
Suleyman Gulsuner, Dan J Stein, Ezra S Susser, Goodman Sibeko, A Pretorius, Tom Walsh, L Majara, M M Mndini, S G Mqulwana, O A Ntola, Silvia Casadei, Linda Ngqengelele, Viktoriya Korchina, Celia van der Merwe, Megan Pool, Kim Fader, M Feng, Emily A Willoughby, Donna M Muzny, A Baldinger, H F Andrews, Ruben E Gur, Richard A Gibbs, Zukiswa Zingela, Mohammed Nagdee, Rajkumar Ramesar, Mary-Claire King, Jon M McClellan
Genetics of schizophrenia in the South African Xhosa. Science (New York, N.Y.) 367 (6477) (2020)
Tom Walsh, Silvia Casadei, Katherine M Munson, Mary Eng, Jessica B Mandell, Suleyman Gulsuner, Mary-Claire King
CRISPR-Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes. Journal of medical genetics 58 (12) (2020)
Zippora Brownstein, Suleyman Gulsuner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov, Ming K Lee, Mor Bordeynik-Cohen, Maria Birkan, Weise Chang, Silvia Casadei, Nada Danial-Farran, Amal AbuRayyan, Ryan J Carlson, Lara Kamal, Asgeir Ö Arnthórsson, Meirav Sokolov, Dror Gilony, Noga Lipschitz, Moshe Frydman, Bella Davidov, Michal Macarov, Michal Sagi, Chana Vinkler, Hana Poran, Reuven Sharony, Nadra Samra, Na'ama Zvi, Hagit Baris-Feldman, Amihood Singer, Ophir Handzel, Ronna Hertzano, Doaa Ali-Naffaa, Noa Ruhrman-Shahar, Ory Madgar, Efrat Sofrin-Drucker, Amir Peleg, Morad Khayat, Mordechai Shohat, Lina Basel-Salmon, Elon Pras, Dorit Lev, Michael Wolf, Eirikur Steingrimsson, Noam Shomron, Matthew William Kelley, Moien N Kanaan, Stavit Allon-Shalev, Mary-Claire King, Karen B Avraham
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1. Clinical genetics 98 (4) (2020)
Amal AbuRayyan, Lara Kamal, Silvia Casadei, Zippora Brownstein, Fouad Zahdeh, Hashem Shahin, Christina Canavati, Dima Dweik, Tamara Jaraysa, Grace Rabie, Ryan J Carlson, Suleyman Gulsuner, Ming K Lee, Karen B Avraham, Tom Walsh, Mary-Claire King, Moien N Kanaan
Genomic analysis of inherited hearing loss in the Palestinian population. Proceedings of the National Academy of Sciences of the United States of America 117 (33) (2020)