ThomasSlavinJr.MD

PubMed

• 96 citations
  Circulating tumor DNA as an early cancer detection tool.
  Andrea Campos-Carrillo, Jeffrey N. Weitzel, Prativa Sahoo, Russell C. Rockne, Janet V. Mokhnatkin, Muhammed Murtaza, Stacy W. Gray, Laura H. Goetz, Ajay Goel, Nicholas...> ;Pharmacology & Therapeutics. 2020 Mar 1
• 2 citations
  Experience Gained from the Development and Execution of a Multidisciplinary Multi-syndrome Hereditary Colon Cancer Family Conference
  Ilana Solomon, Christina Rybak, Lily R. Van Tongeren, Lili Kuzmich, Kathleen R. Blazer, Bita Nehoray, Mariana Niell-Swiller, Shawnie Bray, Travis Bray, Karen Hurley, J...> ;Journal of Cancer Education. 2019 Dec 1
• 21 citations
  Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing.
  Thomas P. Slavin, Bradford Coffee, Ryan Bernhisel, Jennifer Logan, Hannah C. Cox, Guido Marcucci, Jeffrey N. Weitzel, Susan L. Neuhausen, Debora Mancini-DiNardo> ;Cancer Genetics. 2019 Apr 13
• 9 citations
  The Burden of Breast Cancer Predisposition Variants Across The Age Spectrum Among 10 000 Patients
  Yanin Chavarri-Guerra, Carolyn B. Hendricks, Sandra Brown, Catherine A. Marcum, Mary Hander, Zdenka E Segota, Chris Hake, Sharon Sand, Thomas P. Slavin, Arti Hurria, E...> ;Journal of the American Geriatrics Society. 2019 May 1
• 33 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 Jan 11
• 97 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, Elizabeth C. Chao, Katherine Dixon, Joana Figueiredo, Rajarshi Ghosh, David G. Hunt...> ;Human Mutation. 2018 Nov 1
• Therapy-related acute lymphoblastic leukemia has distinct clinical and cytogenetic features compared to <i>de novo</i> acute lymphoblastic leukemia, but outcomes are c...
  Aldoss, I., Stiller, T., Tsai, N., Song, J. Y., Cao, T., Bandara, N. A., Salhotra, A., Khaled, S. K., Aribi, A., Malki, M. M., Mei, M., Ali, H., Spielberger, R., O'Don...> ;Haematologica. 2018 Jun 16
• Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry.
  Slavin, T. P., Van Tongeren, L. R., Behrendt, C. E., Solomon, I., Rybak, C., Nehoray, B., Kuzmich, L., Niell-Swiller, M., Blazer, K. R., Tao, S., Yang, K., Culver, J. ...> ;Journal of the National Cancer Institute. 2018 Apr 5
• Rlip Depletion Prevents Spontaneous Neoplasia in TP53 Null Mice
  Thomas P Slavin, Sanjay Awasthi, Joshua Tompkins, Jeffrey N Weitzel> ;Proceedings of the National Academy of Sciences.
• 35 citations
  Genetic Gastric Cancer Susceptibility in the International Clinical Cancer Genomics Community Research Network
  Thomas P. Slavin, Susan L. Neuhausen, Christina Rybak, Ilana Solomon, Bita Nehoray, Kathleen R. Blazer, Mariana Niell-Swiller, Aaron Adamson, Yate-Ching Yuan, Kai Yang...> ;Cancer Genetics. 2017 Oct 1
• 24 citations
  The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.
  Thomas P. Slavin, Susan L. Neuhausen, Bita Nehoray, Mariana Niell-Swiller, Ilana Solomon, Christina Rybak, Kathleen R. Blazer, Aaron Adamson, Kai Yang, Sharon Sand, Na...> ;Familial Cancer. 2018 Apr 1
• Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
  Vigorito, E., Kuchenbaecker, K. B., Beesley, J., Adlard, J., Agnarsson, B. A., Andrulis, I. L., Arun, B. K., Barjhoux, L., Belotti, M., Benitez, J., Berger, A., Bojese...> ;PloS one. 2016 Jul 28
• 88 citations
  Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer
  Kara N. Maxwell, Steven N. Hart, Joseph Vijai, Kasmintan A. Schrader, Thomas P. Slavin, Tinu Thomas, Bradley Wubbenhorst, Vignesh Ravichandran, Raymond Moore, Chunling...> ;American Journal of Human Genetics. 2016 May 5
• 2 citations
  Is Tel Hashomer camptodactyly a distinct clinical entity
  A. Mochizuki, J. Hyland, T. Brown, T.P. Slavin> ;American Journal of Medical Genetics. Part A. 2015 Jan 1
• 9 citations
  The perinatal presentation of cardiofaciocutaneous syndrome.
  Kara N. Wong Ramsey, Matthew H. Loichinger, Thomas P. Slavin, Sheree Kuo, Laurie H. Seaver> ;American Journal of Medical Genetics. Part A. 2014 Aug 1
• 18 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, Thomas P. Slavin> ;World Journal of Cardiology. 2014 May 26
• 15 citations
  Genetic associations of relaxin: preterm birth and premature rupture of fetal membranes.
  Frederico G. Rocha, Thomas P. Slavin, Dongmei Li, Maarit Tiirikainen, Gillian D. Bryant-Greenwood> ;American Journal of Obstetrics and Gynecology. 2013 Sep 1
• Response to “germline mosaicism in cornelia de lange syndrome: Dilemmas and risk figures” by mariani et al.
  Thomas P. Slavin, Ian D. Krantz> ;American Journal of Medical Genetics. Part A. 2013 Jul 1
• 3 citations
  Bilateral Radial Ulnar Synostosis and Vertebral Anomalies in a Child with a De Novo 16p13.3 Interstitial Deletion
  Allison Tam, Kit Shan Lee, Sansan Lee, William Burkhalter, Lucio U. Pascua, Thomas P. Slavin> ;Case Reports in Genetics. 2013 Jul 1
• 4 citations
  Clinical Presentation and Positive Outcome of Two Siblings with Holocarboxylase Synthetase Deficiency Caused by a Homozygous L216R Mutation.
  T. P. Slavin, S. J. Zaidi, C. Neal, B. Nishikawa, L. H. Seaver> ;JIMD Reports. 2013 Sep 13
• 9 citations
  Haploinsufficiency of STK11 and neighboring genes cause a contiguous gene syndrome including Peutz-Jeghers phenotype.
  Sarah Scollon, Kirsty McWalter, Keith K. Abe, Jeremy King, Kevin Kimata, Thomas P. Slavin> ;American Journal of Medical Genetics. Part A. 2012 Nov 1
• 4 citations
  Microarray comparative genomic hybridization and cytogenetic characterization of tissue-specific mosaicism in three patients.
  Elena A. Repnikova, Caroline Astbury, Shalini C. Reshmi, Sarah N. Ramsey, Joan F. Atkin, Devon Lamb Thrush, Anna L. Mitchell, Robert E. Pyatt, Kristina M. Reber, Thoma...> ;American Journal of Medical Genetics. Part A. 2012 Aug 1
• 26 citations
  Germline mosaicism in Cornelia de Lange syndrome
  Thomas P. Slavin, Noam Lazebnik, Dinah Clark, Jaime Vengoechea, Leslie Cohen, Maninder Kaur, Laura Konczal, Carol A. Crowe, Jane E. Corteville, Małgorzata J.M. Nowaczy...> ;American Journal of Medical Genetics. Part A. 2012 Jun 1
• 19 citations
  Monozygotic twins discordant for trisomy 13.
  K Wong Ramsey, T P Slavin, G Graham, G I Hirata, V Balaraman, Laurie H. Seaver> ;Journal of Perinatology. 2012 Apr 1
• 65 citations
  Two-marker association tests yield new disease associations for coronary artery disease and hypertension
  Thomas P. Slavin, Tao Feng, Audrey H. Schnell, Xiaofeng Zhu, Robert C. Elston> ;Human Genetics. 2011 May 28
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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

• 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
• 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
• 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
• 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
• 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
• 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 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
• Chemoprevention in Hereditary Gastrointestinal Cancer Syndromes. 
  City of Hope - 1/18/2015
• Identifying hereditary pancreatic and gastric cancer predisposition using a large high risk cohort. 
  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
• Dysmorphology potpourri. 
  Kapi'olani Medical Center for Women and Children - 1/28/2013
• Hawai'i Newborn Screening. 
  1/28/2013
• "Genetic testing in cancer" 
  Ala Moana Hotel Ballroom - 1/23/2013
• Multifactorial inheritance and common birth defects. 
  Kapi'olani Medical Center for Women and Children - 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