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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

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Tom Walsh

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Haematologica|September 21, 2014

Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexityMichael Y Zhang, Siobán B Keel, Tom Walsh, et al.

Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|August 8, 2016

Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived MalignancyKatarzyna Rojek, Eric Nickels, Barbara Neistadt, et al.

Gastroenterology|March 1, 2017

Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and SurveillanceSari Lieberman, Tom Walsh, Menachem Schechter, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 5, 2020

Genomic analysis of inherited hearing loss in the Palestinian populationAmal Abu Rayyan, Lara Kamal, Silvia Casadei, et al.

JAMA Oncology|February 6, 2016

Somatic Mosaic Mutations in PPM1D and TP53 in the Blood of Women With Ovarian CarcinomaElizabeth M Swisher, Maria I Harrell, Barbara M Norquist, et al.

Neurology|May 11, 2016

Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infectionAdi Aran, Nuphar Rosenfeld, Ranit Jaron, et al.

International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|August 14, 2022

Placenta accreta spectrum ultrasound stage and fetal growthHelena C Bartels, Jennifer M Walsh, Clare O'Connor, et al.

Journal of the National Cancer Institute|December 14, 2024

TP53 missense allele predisposing to high risk of breast cancer but not pediatric cancersSuhair Lolas-Hamameh, Sari Lieberman, Alaa Sarahneh, et al.

Cancer|December 8, 2015

Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy-related leukemiaJane E Churpek, Rafael Marquez, Barbara Neistadt, et al.

American Journal of Human Genetics|July 7, 2010

Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51Tom Walsh, Sarah B Pierce, Danielle R Lenz, et al.

Pageof 20

Search research articles

Showing results (141-150 of 193) with videos related to

Sort By:

Pageof 20

Haematologica|September 21, 2014

Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexityMichael Y Zhang, Siobán B Keel, Tom Walsh, et al.

Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|August 8, 2016

Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived MalignancyKatarzyna Rojek, Eric Nickels, Barbara Neistadt, et al.

Gastroenterology|March 1, 2017

Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and SurveillanceSari Lieberman, Tom Walsh, Menachem Schechter, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 5, 2020

Genomic analysis of inherited hearing loss in the Palestinian populationAmal Abu Rayyan, Lara Kamal, Silvia Casadei, et al.

JAMA Oncology|February 6, 2016

Somatic Mosaic Mutations in PPM1D and TP53 in the Blood of Women With Ovarian CarcinomaElizabeth M Swisher, Maria I Harrell, Barbara M Norquist, et al.

Neurology|May 11, 2016

Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infectionAdi Aran, Nuphar Rosenfeld, Ranit Jaron, et al.

International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|August 14, 2022

Placenta accreta spectrum ultrasound stage and fetal growthHelena C Bartels, Jennifer M Walsh, Clare O'Connor, et al.

Journal of the National Cancer Institute|December 14, 2024

TP53 missense allele predisposing to high risk of breast cancer but not pediatric cancersSuhair Lolas-Hamameh, Sari Lieberman, Alaa Sarahneh, et al.

Cancer|December 8, 2015

Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy-related leukemiaJane E Churpek, Rafael Marquez, Barbara Neistadt, et al.

American Journal of Human Genetics|July 7, 2010

Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51Tom Walsh, Sarah B Pierce, Danielle R Lenz, et al.

Pageof 20