Center-Authored Papers

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Zhang MY, Churpek JE, Keel SB, Walsh T, Lee MK, Loeb KR, Gulsuner S, Pritchard CC, Sanchez-Bonilla M, Delrow JJ et al..  2015.  Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy.. Nature genetics. 47(2):180-5. Abstract
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Swisher EM, Gonzalez RM, Taniguchi T, Garcia RL, Walsh T, Goff BA, Welcsh P.  2009.  Methylation and protein expression of DNA repair genes: association with chemotherapy exposure and survival in sporadic ovarian and peritoneal carcinomas.. Molecular cancer. 8:48. Abstract
Steinberg-Shemer O, Keel S, Dgany O, Walsh T, Noy-Lotan S, Krasnov T, Yacobovich J, Quarello P, Ramenghi U, King M-C et al..  2016.  Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis.. Journal of pediatric hematology/oncology. Abstract
Seo A, Walsh T, Lee M, Ho P, Hsu EK, Sidbury R, King M-C, Shimamura A.  2016.  FAM111B Mutation Is Associated With Inherited Exocrine Pancreatic Dysfunction.. Pancreas. 45(6):858-862. Abstract
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Rojek K, Nickels E, Neistadt B, Marquez R, Wickrema A, Artz A, van Besien K, Larson RA, Lee MK, Segal JP et al..  2016.  Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. Abstract
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Pritchard CC, Salipante SJ, Koehler K, Smith C, Scroggins S, Wood B, Wu D, Lee MK, Dintzis S, Adey A et al..  2014.  Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens.. The Journal of molecular diagnostics : JMD. 16(1):56-67. Abstract
Pritchard CC, Mateo J, Walsh MF, DeSarkar N, Abida W, Beltran H, Garofalo A, Gulati R, Carreira S, Eeles R et al..  2016.  Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.. The New England journal of medicine. 375(5):443-453. Abstract
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Lewinsohn M, Brown AL, Weinel LM, Phung C, Rafidi G, Lee MK, Schreiber AW, Feng J, Babic M, Chong C-E et al..  2015.  Novel germline DDX41 mutations define families with a lower age of MDS/AML onset, and lymphoid malignancies.. Blood. Abstract
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Keel SB, Scott A, Sanchez-Bonilla M, Ho PA, Gulsuner S, Pritchard CC, Abkowitz JL, King M-C, Walsh T, Shimamura A.  2016.  Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.. Haematologica. Abstract
Kazenwadel J, Secker GA, Liu YJ, Rosenfeld JA, Wildin RS, Cuellar-Rodriguez J, Hsu AP, Dyack S, Fernandez CV, Chong C-E et al..  2012.  Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature.. Blood. 119(5):1283-1291. Abstract
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Dorschner MO, Amendola LM, Turner EH, Robertson PD, Shirts BH, Gallego CJ, Bennett RL, Jones KL, Tokita MJ, Bennett JT et al..  2013.  Actionable, pathogenic incidental findings in 1,000 participants' exomes.. American journal of human genetics. 93(4):631-40. Abstract