ThomasSlavinJr.MD

PubMed

• 34 citations
  The effects of genomic germline variant reclassification on clinical cancer care.
  Thomas P. Slavin, Sophia Manjarrez, Colin C. Pritchard, Stacy W. Gray, Jeffrey N. Weitzel
  Oncotarget. 2019-01-11
• 106 citations
  Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants
  Kristy Lee, Kate Krempely, Maegan E. Roberts, Michael J. Anderson, Fátima Carneiro
  Human Mutation. 2018-11-01
• 19 citations
  Elevated blood pressure: Our family's fault? The genetics of essential hypertension.
  Aniket Natekar, Randi L Olds, Meghann W Lau, Kathleen Min, Karra Imoto
  World Journal of Cardiology. 2014-05-26

Journal Articles

• Specifications of the ACMG/AMP Variant Curation Guidelines for the Analysis of Germline CDH1 Sequence Variants  
  Sharon E Plon, Chimene Kesserwan, Thomas P Slavin, Liying Zhang, Human Mutation
• Clinical application of multigene panels: challenges of next-generation counseling and cancer risk management  
  Slavin TP, Niell-Swiller M, Solomon I, Nehoray B, Rybak C, Blazer KR, Weitzel JN, Front. Oncol., 1/29/2015
• Congenital diaphragmatic hernia in a fetus with a de novo terminal deletion of chromosome 15q261  
  Ruth C, Starcevic J, Bartholomew ML, Qin N, Slavin TP, Hereditary Genetics, 1/1/2012

Books/Book Chapters

• Genomic and Personalized Medicine 
  Chapter: The Genomics of Colorectal Cancer. 
  Wiesner GL, Slavin T, Barnholtz-Sloan JEditors: Willard and Ginzberg.Elsevier, Inc.2008

Abstracts/Posters

• How big of a role does TP53 play in BRCA1/2 negative familial breast cancer? Data from the SIMPLEXO consortium.
  Slavin TP, Maxwell KN, Hart S, Vijai J, Schrader K, Guidugli L, Thomas T, Moore R, Hu C, Wubbenhorst B, Domchek SM, Robson ME, Radice P, Peterlongo P, Ford J, Garber J..., American Society of Human Genetics Annual Meeting, Baltimore, MD, 1/1/2015
• The contribution of high and moderate penetrance breast cancer susceptibility genes to familial breast cancer risk in BRCAx families.
  Maxwell KN, Hart S, Vijai J, Schrader K, Slavin TP, Thomas T, Moore R, Hu C, Wubbenhorst B, Domchek SM, Robson ME, Radice P, Peterlongo P, Ford J, Garber J, Szabo C, N..., American Society of Human Genetics Annual Meeting, 1/1/2015
• Hereditary susceptibility to pancreatic cancer.
  Raja S, Sand S, Weitzel JN, Yang K, Slavin TP, Eugene and Ruth Roberts Summer Academy Poster Presentation, City of Hope, Duarte, CA, 1/1/2015
• Sarcoma, a Lynch syndrome associated malignancy?
  Kaczmar J, Everett JN, Ruth K, Stoffel EM, Stoll J, Kupfer SS, Hampel H, Stadler ZK, Gaddam P, Rybak CC, Slavin TP, Terdiman JP, Blanco A, Hall MJ, American Society Clinical Oncology Annual Meeting, Chicago, IL, 1/1/2015
• Assessment of the clinical presentation of patients with at least two deleterious mutations on multi-gene panel testing.
  Weitzel JN, Blazer KR, Nehoray B, Kidd J, Slavin TP, Solomon I, Niell-Swiller M, Rybak, C, Saam J, American Society Clinical Oncology Annual Meeting, Chicago, IL, 1/1/2015
• Multiplex Identification of genetic etiologies among women with bilateral breast cancer using a 25gene hereditary cancer panel.
  Weitzel JN, Blazer KR, Nehoray B, Kidd J, Slavin TP, Solomon I, Niell-Swiller M, Rybak C, Saam J, Lancaster J, San Antonio Breast Cancer Symposium, NM, 1/1/2015
• Perinatal Presentation of Cardiofaciocutaneous Syndrome.
  Ramsey KW, Slavin TP, Loichinger M, Kuo S, Thompson K, Seaver L, Pediatric Academic Societies and Asian Society for Pediatric Research Meeting, JABSOM Biomedical Sciences and Health Disparities Symposium, Vancouver, Canada; Honolulu, HI, Apr 2014, 1/1/2014
• 25 year old female with lifelong asymmetric weakness diagnosed with X-linked myotubular myopathy (XLMTM) after delivery of hypotonic twin boys.
  Grosmann CM, Leshner RT, Malicki DM, Sahagian ML, Slavin TP, Willis MJ, Mestre L, Muscular Dystrophy Association Annual Conference, Chicago IL, 1/1/2014
• The genetics of hereditary essential hypertension.
  Natekar, A, Olds R, Lau M, Imoto K, Slavin TP, JABSOM Biomedical Sciences and Health Disparities Symposium, Honolulu, HI, 1/1/2014
• A Novel Work up for Evaluation of Possible TSC in Patients with Angiomyolipomas.
  Kurosawa G, Glaser, D, Thompson K, Slavin TP, JABSOM Biomedical Sciences and Health Disparities Symposium, Honolulu, HI, 1/1/2014
• Expanding the BP1-BP2 15q11.2 Microdeletion Phenotype: Tracheoesophageal Fistula and Congenital Cataracts.
  Wong D, Johnson SM, Young D, Iwamoto L, Sood S, Slavin TP, JABSOM Biomedical Sciences and Health Disparities Symposium, Honolulu, HI, 1/1/2014
• The Utility of Clinical Whole Exome Sequencing in the Diagnosis of Multiple Genetic Diseases.
  Hardison M, Koenig MK, Slavin T, Beuten J, Eng C, Yang Y, American College of Medical Genetics Annual Clinical Genetics Meeting, Phoenix, AZ, 1/1/2013
• Clinical presentation and outcome of two siblings with holocarboxylase synthetase deficiency caused by a homozygous L216R mutation.
  Slavin TP, Zaidi SJ, Neal C, Kyono W, Nishikawa B, Seaver L, American College of Medical Genetics Annual Clinical Genetics Meeting, Phoenix, AZ, 1/1/2013
• Genetic susceptibility to preterm birth in the Filipino population in Hawaii.
  Rocha F, Slavin T, Li D, Yamamoto S, Bryant-Greenwood G, Am J Obstet Gynecol, Society for Maternal Fetal Medicine Annual Meeting, San Francisco, CA, 1/1/2013
• Bilateral radioulnar synostosis and vertebral anomalies in a child with a de novo 16p13.3 interstitial deletion.
  Slavin TP, Tam A, Lee K, Lee S, Pascua L, Burkhalter W, American Society of Human Genetics Annual Meeting, San Francisco, CA, 1/1/2012
• Molecular and cytogenetic characterization of lineage-specific mosaicism in a female patient with del(14)(q32.2).
  Repnikova EA, Slavin T, Mitchell A, Brock A, Erdman L, Deeg C, Hedrick S, Ramsey S, Lamb TD, Reshmi SC, Astbury C, Pyatt R, Gastier-Foster J, American College of Medical Genetics Annual Meeting, Albuquerque, NM, 1/1/2010
• Cornelia de Lange Syndrome: germline mosaicism, prenatal and pregnancy findings.
  Slavin TP, Lazebnik N, American Society of Human Genetics Annual Meeting, Honolulu, HI, 1/1/2009
• Proximal 4p deletion syndrome.
  Slavin TP, Curtis C, McCandless SE, American College of Medical Genetics Annual Meeting, Tampa, FL, 1/1/2009
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Lectures

• Effect of germline ATM mutations on clonal hematopoiesis. 
  2019 ASCO Annual Meeting - 6/1/2019
• Understanding the NGS Test report: a primer on genomics nomenclature. 
  1/27/2015
• Updates in Li Fraumeni syndrome screening. 
  City of Hope - 1/26/2015
• Identifying hereditary pancreatic and gastric cancer predisposition using the Clinical Cancer Genomics Community Research Network. 
  City of Hope - 1/20/2015
• Identifying hereditary pancreatic and gastric cancer predisposition using a large high risk cohort. 
  City of Hope - 1/18/2015
• Chemoprevention in Hereditary Gastrointestinal Cancer Syndromes. 
  City of Hope - 1/18/2015
• The role of genetics and survivorship. 
  City of Hope Antelope Valley, Lancaster, CA - 1/14/2015
• Colon and other non-breast cancer genetics. 
  City of Hope - 1/5/2015
• Next Generation Genetic Cancer Risk Assessments. 
  Good Samaritan Hospital, Los Angeles - 1/4/2015
• Genetic syndromes III. 
  Kapi'olani Medical Center for Women and Children, 2013 - 1/30/2014
• Congenital anomalies of the newborn. 
  Sheraton Wakkiki, HI - 1/25/2014
• Genetic syndromes II. 
  Kapi'olani Medical Center for Women and Children, 2013, 2012 - 1/23/2014
• Common recognizable syndromes. 
  Kapi'olani Medical Center for Women and Children, 2011 - 1/12/2014
• Molecular diagnostic techniques. 
  Kapi'olani Medical Center for Women and Children - 1/11/2014
• Genetic syndromes I. 
  Kapi'olani Medical Center for Women and Children, 2013, 2012 - 1/9/2014
• Pharmacogenomics. 
  Kapi'olani Medical Center for Women and Children - 1/7/2014
• Craniosynostoses; don't forget the hands and feet! 
  Kapi'olani Medical Center for Women and Children - 1/6/2014
• Molecular genetics. 
  The Queen's Medical Center, Honolulu, HI - 1/6/2014
• Cardiac syndromes 
  The Queen's Medical Center, Honolulu, HI - 1/2/2014
• Pharmacogenomics for the adult physician. 
  1/29/2013
• Hawai'i Newborn Screening. 
  1/28/2013
• Dysmorphology potpourri. 
  Kapi'olani Medical Center for Women and Children - 1/28/2013
• Multifactorial inheritance and common birth defects. 
  Kapi'olani Medical Center for Women and Children - 1/23/2013
• "Genetic testing in cancer" 
  Ala Moana Hotel Ballroom - 1/23/2013
• Molecular genetics III. 
  Kapi'olani Medical Center for Women and Children - 1/23/2013
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Other

• "Genodermatoses in cancer" 
  Slavin TP, Intensive Course in Cancer Genetics (Video)
  City of Hope - 1/10/2014
• Visual Diagnosis: Newborn with Unilateral Lower Extremity Vascular Malformation and Limb Asymmetry. 
  Wong Ramsey K, Slavin TP, Tjoeng T, Jain S, NeoReviews Vol. 15 No. 2
  http://neoreviews.aappublications.org/content/15/2/e82.short
  1/1/2014
• "Genetic Testing" 
  Slavin TP, The Body Show with Kathy Kozak, Hawai'i Public Radio
  1/10/2013