2001 Polaris Pkwy
Columbus, OH 43240
Phone: (614) 293-9099
Associate Professor-Clinical, Human Genetics
My undergraduate training was completed at the University of Iowa in Iowa City, IA. I graduated in 1992 with a Bachelor’s of Science in Biology with a minor in English. I then worked as a Research Assistant in the Department of Physiology and Biophysics at the University of Iowa, where I worked for 2 years on gene transcription in Drosophila melanogaster. In June 1996, I completed my Master’s of Science in Genetic Counseling at the University of Minnesota in Minneapolis, MN. In June 1999, I received my Board Certification from the American Board of Genetic Counseling.
Between July 1996 and October 2002, I was a Genetic Counselor in the Center for Human Genetics at Case Western Reserve University/University Hospitals of Cleveland in Cleveland, Ohio. In 1999, I was appointed to Clinical Instructor of Medicine. I came to The Ohio State University in October 2002 as a Genetic Counselor and Clinical Instructor of Medicine in the Clinical Cancer Genetics Program in the Division of Human Genetics, Department of Internal Medicine. I was promoted to Clinical Assistant Professor of Internal Medicine in the auxiliary track in 2005. In 2010, I was appointed Assistant Professor, Clinical Internal Medicine and in 2012, Associate Professor Clinical Internal Medicine.
My clinical responsibilities include counseling patients and families with a variety of different cancer susceptibility syndromes about cancer risks, genetic testing, and medical management. I currently staff two half day clinics a week in the Division of Human Genetics. In addition to my clinical duties, I have an active research role within the OSU Thyroid Cancer Unit led by Dr. Matthew Ringel. I am a Core co-leader and co-investigator on an NCI-funded P01 entitled "Genetic Signalling Pathways in Epithelial Thyroid Cancer". I am also the clinical co-Leader of Project 1, "Low-Penetrance Genes in the Predisposition to Papillary Thyroid Cancer", on a more recently awarded NCI-funded SPORE. I am active in the National Society of Genetic Counselors (NSGC) and have a national reputation as a leader. I have served on the Board of Directors of NSGC since 2010. Since my last promotion, I was elected President of the Society. This is the highest elected position in the society.
|2013 - present||Tim Shen The Ohio State University.|
|2006 - 2008||Amanda Knoth The Ohio State University. Graduated 2008.|
|2008 - 2011||Brandon Smith The Ohio State University. Graduated 2011.|
|1999 - present||Diplomate: American Board of Genetic Counseling|
|2013 - present||Genetic Counselor: State Medical Board of Ohio|
|07/01/2009||Hereditary Cancer Clinic (Polaris Innovation Centre)|
|1992||B.S., University of Iowa|
|1996||M.S., University of Minnesota|
|2002 - 2005||Journal of Medical Genetics|
|2004 - present||NCI Physician Data Query (PDQ) Cancer Genetics editorial board|
|2010 - present||Thyroid|
|2011 - present||Genetics in Medicine|
|2011 - present||Frontiers in Thyroid Endocrinology|
|2011 - present||Journal of Genetic Counseling|
|2010 - present||NIH Award of Merit. National Institutes of Health.|
Anderson MG, Perkins GL, Chittick P, Shrigley RJ, Johnson WA. "drifter, a Drosophila POU-domain transcription factor, is required for correct differentiation and migration of tracheal cells and midline glia." Genes and Development. Vol. 9, no. 1. (January 1995.): 123-137.
Certel K, Anderson MG, Shrigley RJ, Johnson WA. "Distinct variant DNA-binding sites determine cell-specific autoregulated expression of the Drosophila POU domain transcription factor drifter in midline glia and trachea." MOLECULAR AND CELL BIOLOGY. Vol. 16, no. 4. (April 1996.): 1813-1823.
Rose P, Shrigley R, Wiesner GL. "Germline BRCA2 mutation in a patient with fallopian tube carcinoma: a case report." GYNECOLOGIC ONCOLOGY. Vol. 77, (May 2000.): 319-20.
Nagy R, Sweet K, Eng C. "Highly penetrant hereditary cancer syndromes." ONCOGENE. Vol. 23, no. 38. (August 2004.): 6445-70.
He H, Olesnanik K, Nagy R, Liyanarachchi S, Prasad ML, Stratakis CA, Kloos RT, de la Chapelle A. "Allelic Variation in Gene Expression in Thyroid Tissue." THYROID. Vol. 15, no. 7. (July 2005.): 660-667.
He H, Jazdzewski K, Li W, Liyanarachchi S, Nagy R, Volinia S, Calin GA, Liu C-G, Franssila K, Suster S, Kloos RT, Croce CM, de la Chapelle A. "The role of micro-RNA genes in papillary thyroid carcinoma.." PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES. Vol. 102, no. 52. (January 2005.): 19075-80.
Yoon,Heejei; He,Huiling; Nagy,Rebecca; Davuluri,Ramana; Suster,Saul; Schoenberg,Daniel; Pellegata,Natalia; de la Chapelle,Albert. "Identification of a novel noncoding RNA gene, NAMA, that is downregulated in papillary thyroid carcinoma with BRAF mutation and associated with growth arrest." INTERNATIONAL JOURNAL OF CANCER. Vol. 121, no. 4. (August 2007.): 767-775.
Leib J, Hoodfar E, Larsen Haidle J, Nagy R. "The new genetic privacy law: How GINA will affect patients seeking counseling and testing for inherited cancer risk.." Community Oncology. Vol. 5, no. 6. (January 2008.): 351-354.
He,Huiling; Nagy,Rebecca; Liyanarachchi,Sandya; Jiao,Hong; Li,Wei; Suster,Saul; Kere,Juha; de la Chapelle,Albert. "A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24." CANCER RESEARCH. Vol. 69, no. 2. (January 2009.): 625-631.
Gudmundsson,Julius; Sulem,Patrick; Gudbjartsson,Daniel,F; Jonasson,Jon,G; Sigurdsson,Asgeir; Bergthorsson,Jon,T; He,Huiling; Blondal,Thorarinn; Geller,Frank; Jakobsdottir,Margret; Magnusdottir,Droplaug,N; Matthiasdottir,Sigurborg; Stacey,Simon,N; Skarphedinsson,Oskar,B; Helgadottir,Hafdis; Li,Wei; Nagy,Rebecca; Aguillo,Esperanza; Faure,Eduardo; Prats,Enrique; Saez,Berta; Martinez,Mariano; Eyjolfsson,Gudmundur,I; Bjornsdottir,Unnur,S; Holm,Hilma; Kristjansson,Kristleifur; Frigge,Michael,L; Kristvinsson,Hoskuldur; Gulcher,Jeffrey,R; Jonsson,Thorvaldur; Rafnar,Thorunn; Hjartarsson,Hannes; Mayordomo,Jose,I; De la Chapelle,Albert; Hrafnkelsson,Jon; Thorsteinsdottir,Unnur; Kong,Augustine; Stefansson,Kari. "Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations." NATURE GENETICS. Vol. 41, no. 4. (April 2009.): 460-464.
Westman,Judith,A; Ferketich,Amy,K; Kauffman,Ross,M; MacEachern,Steven,N; Wilkins,J,R; Wilcox,Patricia,P; Pilarski,Robert,T; Nagy,Rebecca; Lemeshow,Stanley; De la Chapelle,Albert; Bloomfield,Clara,D. "Low cancer incidence rates in Ohio Amish." CANCER CAUSES & CONTROL. Vol. 21, no. 1. (January 2010.): 69-75.
Iuliano,Rodolfo; Palmieri,Dario; He,Huiling; Iervolino,Angela; Borbone,Eleonora; Pallante,Pierlorenzo; Cianflone,Alessandra; Nagy,Rebecca; Alder,Hansjuerg; Calin,George,A; Trapasso,Francesco; Giordano,Carla; Croce,Carlo,M; De la Chapelle,Albert; Fusco,Alfredo. "Role of PTPRJ genotype in papillary thyroid carcinoma risk." ENDOCRINE-RELATED CANCER. Vol. 17, no. 4. (December 2010.): 1001-1006.
Paes,John,E; Hua,Keding; Nagy,Rebecca; Kloos,Richard,T; Jarjoura,David; Ringel,Matthew,D. "The Relationship between Body Mass Index and Thyroid Cancer Pathology Features and Outcomes: A Clinicopathological Cohort Study." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. Vol. 95, no. 9. (September 2010.): 4244-4250.
Nagy,Rebecca; Ganapathi,Shireen; Comeras,Ilene; Peterson,Charissa; Orloff,Mohammed; Porter,Kyle; Eng,Charis; Ringel,Matthew,D; Kloos,Richard,T. "Frequency of Germline PTEN Mutations in Differentiated Thyroid Cancer." THYROID. Vol. 21, no. 5. (May 2011.): 505-510.
Jendrzejewski,Jaroslaw; Tomsic,Jerneja; Lozanski,Gerard; Labanowska,Jadwiga; He,Huiling; Liyanarachchi,Sandya; Nagy,Rebecca; Ringel,Matthew,D; Kloos,Richard,T; Heerema,Nyla,A; de la Chapelle,Albert. "Telomere Length and Telomerase Reverse Transcriptase Gene Copy Number in Patients with Papillary Thyroid Carcinoma." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. Vol. 96, no. 11. (November 2011.): E1876-E1880.
He,Huiling; Liyanarachchi,Sandya; Akagi,Keiko; Nagy,Rebecca; Li,Jingfeng; Dietrich,Rosemary,C; Li,Wei; Sebastian,Nikhil; Wen,Bernard; Xin,Baozhong; Singh,Jarnail; Yan,Pearlly; Alder,Hansjuerg; Haan,Eric; Wieczorek,Dagmar; Albrecht,Beate; Puffenberger,Erik; Wang,Heng; Westman,Judith,A; Padgett,Richard,A; Symer,David,E; de la Chapelle,Albert. "Mutations in U4atac snRNA, a Component of the Minor Spliceosome, in the Developmental Disorder MOPD I." SCIENCE. Vol. 332, no. 6026. (April 2011.): 238-240.
Riley,Bronson,D; Culver,Julie,O; Skrzynia,Cecile; Senter,Leigha,A; Peters,June,A; Costalas,Josephine,W; Callif-Daley,Faith; Grumet,Sherry,C; Hunt,Katherine,S; Nagy,Rebecca,S; McKinnon,Wendy,C; Petrucelli,Nancie,M; Bennett,Robin,L; Trepanier,Angela,M. "Essential Elements of Genetic Cancer Risk Assessment, Counseling, and Testing: Updated Recommendations of the National Society of Genetic Counselors." JOURNAL OF GENETIC COUNSELING. Vol. 21, no. 2. (April 2012.): 151-161.
Jendrzejewski,Jaroslaw; He,Huiling; Radomska,Hanna,S; Li,Wei; Tomsic,Jerneja; Liyanarachchi,Sandya; Davuluri,Ramana,V; Nagy,Rebecca; de la Chapelle,Albert. "The polymorphism rs944289 predisposes to papillary thyroid carcinoma through a large intergenic noncoding RNA gene of tumor suppressor type." PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. Vol. 109, no. 22. (May 2012.): 8646-8651.
Shen,Rulong; Liyanarachchi,Sandya; Li,Wei; Wakely,Paul,E; Saji,Motoyasu; Huang,Jie; Nagy,Rebecca; Farrell,Tisha; Ringel,Matthew,D; De la Chapelle,Albert; Kloos,Richard,T; He,Huiling. "MicroRNA Signature in Thyroid Fine Needle Aspiration Cytology Applied to "Atypia of Undetermined Significance" Cases." THYROID. Vol. 22, no. 1. (January 2012.): 9-16.
Pilarski,Robert; Nagy,Rebecca. "Genetic Testing by Cancer Site: Endocrine System." CANCER JOURNAL. Vol. 18, no. 4. (July 2012.): 364-371.
Nagy,R; Wang,H; Albrecht,B; Wieczorek,D; Gillessen-Kaesbach,G; Haan,E; Meinecke,P; de la Chapelle,A; Westman,J,A. "Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene." CLINICAL GENETICS. Vol. 82, no. 2. (August 2012.): 140-146.
Gudmundsson,Julius; Sulem,Patrick; Gudbjartsson,Daniel,F; Jonasson,Jon,G; Masson,Gisli; He,Huiling; Jonasdottir,Aslaug; Sigurdsson,Asgeir; Stacey,Simon,N; Johannsdottir,Hrefna; Helgadottir,Hafdis,Th; Li,Wei; Nagy,Rebecca; Ringel,Matthew,D; Kloos,Richard,T; de Visser,Marieke,CH; Plantinga,Theo,S; den Heijer,Martin; Aguillo,Esperanza; Panadero,Angeles; Prats,Enrique; Garcia-Castano,Almudena; De Juan,Ana; Rivera,Fernando; Walters,G,Bragi; Bjarnason,Hjordis; Tryggvadottir,Laufey; Eyjolfsson,Gudmundur,I; Bjornsdottir,Unnur,S; Holm,Hilma; Olafsson,Isleifur; Kristjansson,Kristleifur; Kristvinsson,Hoskuldur; Magnusson,Olafur,T; Thorleifsson,Gudmar; Gulcher,Jeffrey,R; Kong,Augustine; Kiemeney,Lambertus,ALM; Jonsson,Thorvaldur; Hjartarson,Hannes; Mayordomo,Jose,I; Netea-Maier,Romana,T; De la Chapelle,Albert; Hrafnkelsson,Jon; Thorsteinsdottir,Unnur; Rafnar,Thorunn; Stefansson,Kari. "Discovery of common variants associated with low TSH levels and thyroid cancer risk." NATURE GENETICS. Vol. 44, no. 3. (March 2012.): 319-U126.
Nagy,Rebecca. "Walk with me. Incoming Presidential address of the National Society of Genetic Counselors." JOURNAL OF GENETIC COUNSELING. Vol. 22, no. 1. (February 2013.): 1-3.
He,Huiling; Bronisz,Agnieszka; Liyanarachchi,Sandya; Nagy,Rebecca; Li,Wei; Huang,Yungui; Akagi,Keiko; Saji,Motoyasu; Kula,Dorota; Wojcicka,Anna; Sebastian,Nikhil; Wen,Bernard; Puch,Zbigniew; Kalemba,Michal; Stachlewska,Elzbieta; Czetwertynska,Malgorzata; Dlugosinska,Joanna; Dymecka,Kinga; Ploski,Rafal; Krawczyk,Marek; Morrison,Patrick,J; Ringel,Matthew,D; Kloos,Richard,T; Jazdzewski,Krystian; Symer,David,E; Vieland,Veronica,J; Ostrowski,Michael; Jarzab,Barbara; de la Chapelle,Albert. "SRGAP1 Is a Candidate Gene for Papillary Thyroid Carcinoma Susceptibility." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. Vol. 98, no. 5. (May 2013.): E973-E980.
La Perle,Krista,MD; Kim,Dong,Chul; Hall,Nathan,C; Bobbey,Adam; Shen,Daniel,H; Nagy,Rebecca,S; Wakely,Paul,E; Lehman,Amy; Jarjoura,David; Jhiang,Sissy,M. "Modulation of Sodium/Iodide Symporter Expression in the Salivary Gland." THYROID. Vol. 23, no. 8. (August 2013.): 1029-1036.
Liyanarachchi,Sandya; Wojcicka,Anna; Li,Wei; Czetwertynska,Malgorzata; Stachlewska,Elzbieta; Nagy,Rebecca; Hoag,Kevin; Wen,Bernard; Ploski,Rafal; Ringel,Matthew,D; Kozlowicz-Gudzinska,Izabella; Gierlikowski,Wojciech; Jazdzewski,Krystian; He,Huiling; de la Chapelle,Albert. "Cumulative Risk Impact of Five Genetic Variants Associated with Papillary Thyroid Carcinoma." THYROID. Vol. 23, no. 12. (December 2013.): 1532-1540.
He,Huiling; Li,Wei; Wu,Dayong; Nagy,Rebecca; Liyanarachchi,Sandya; Akagi,Keiko; Jendrzejewski,Jaroslaw; Jiao,Hong; Hoag,Kevin; Wen,Bernard; Srinivas,Mukund; Waidyaratne,Gavisha; Wang,Rui; Wojcicka,Anna; Lattimer,Ilene,R; Stachlewska,Elzbieta; Czetwertynska,Malgorzata; Dlugosinska,Joanna; Gierlikowski,Wojciech; Ploski,Rafal; Krawczyk,Marek; Jazdzewski,Krystian; Kere,Juha; Symer,David,E; Jin,Victor; Wang,Qianben; de la Chapelle,Albert. "Ultra-Rare Mutation in Long-Range Enhancer Predisposes to Thyroid Carcinoma with High Penetrance." PLOS ONE. Vol. 8, no. 5. (May 2013.): e61920-.
Nagy, R and Sturm, A. "Personalized medicine: Impact on Patient Care in Genetic Counseling." Current Genetic Medicine Reports. Vol. 1, (March 2013.): 129-134.
Medici,Marco; Porcu,Eleonora; Pistis,Giorgio; Teumer,Alexander; Brown,Suzanne,J; Jensen,Richard,A; Rawal,Rajesh; Roef,Greet,L; Plantinga,Theo,S; Vermeulen,Sita,H; Lahti,Jari; Simmonds,Matthew,J; Husemoen,Lise,LotteN; Freathy,Rachel,M; Shields,Beverley,M; Pietzner,Diana; Nagy,Rebecca; Broer,Linda; Chaker,Layal; Korevaar,Tim,IM; Plia,Maria,Grazia; Sala,Cinzia; Völker,Uwe; Richards,J,Brent; Sweep,Fred,C; Gieger,Christian; Corre,Tanguy; Kajantie,Eero; Thuesen,Betina; Taes,Youri,E; Visser,W,Edward; Hattersley,Andrew,T; Kratzsch,Jürgen; Hamilton,Alexander; Li,Wei; Homuth,Georg; Lobina,Monia; Mariotti,Stefano; Soranzo,Nicole; Cocca,Massimiliano; Nauck,Matthias; Spielhagen,Christin; Ross,Alec; Arnold,Alice; van de Bunt,Martijn; Liyanarachchi,Sandya; Heier,Margit; Grabe,Hans,Jörgen; Masciullo,Corrado; Galesloot,Tessel,E; Lim,E,M; Reischl,Eva; Leedman,Peter,J; Lai,Sandra; Delitala,Alessandro; Bremner,Alexandra,P; Philips,David,IW; Beilby,John,P; Mulas,Antonella; Vocale,Matteo; Abecasis,Goncalo; Forsen,Tom; James,Alan; Widen,Elisabeth; Hui,Jennie; Prokisch,Holger; Rietzschel,Ernst,E; Palotie,Aarno; Feddema,Peter; Fletcher,Stephen,J; Schramm,Katharina; Rotter,Jerome,I; Kluttig,Alexander; Radke,Dörte; Traglia,Michela; Surdulescu,Gabriela,L; He,Huiling; Franklyn,Jayne,A; Tiller,Daniel; Vaidya,Bijay; De Meyer,Tim; Jørgensen,Torben; Eriksson,Johan,G; O'Leary,Peter,C; Wichmann,Eric; Hermus,A,R; Psaty,Bruce,M; Ittermann,Till; Hofman,Albert; Bosi,Emanuele; Schlessinger,David; Wallaschofski,Henri; Pirastu,Nicola; Aulchenko,Yurii,S; De la Chapelle,Albert; Netea-Maier,Romana,T; Gough,Stephen,CL; Meyer zu Schwabedissen,Henriette; Frayling,Timothy,M; Kaufman,Jean-Marc; Linneberg,Allan; Räikkönen,Katri; Smit,Johannes,Wa; Kiemeney,Lambertus,A; Rivadeneira,Fernando; Uitterlinden,André,G; Walsh,John,P; Meisinger,Christa; den Heijer,Martin; Visser,Theo,J; Spector,Timothy,D; Wilson,Scott,G; Völzke,Henry; Cappola,Anne; Toniolo,Daniela; Sanna,Serena; Naitza,Silvia; Peeters,Robin,P. "Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.." PLoS genetics. Vol. 10, no. 2. (February 2014.): e1004123-.
Piotrowski,Arkadiusz; Xie,Jing; Liu,Ying,F; Poplawski,Andrzej,B; Gomes,Alicia,R; Madanecki,Piotr; Fu,Chuanhua; Crowley,Michael,R; Crossman,David,K; Armstrong,Linlea; Babovic-Vuksanovic,Dusica; Bergner,Amanda; Blakeley,Jaishri,O; Blumenthal,Andrea,L; Daniels,Molly,S; Feit,Howard; Gardner,Kathy; Hurst,Stephanie; Kobelka,Christine; Lee,Chung; Nagy,Rebecca; Rauen,Katherine,A; Slopis,John,M; Suwannarat,Pim; Westman,Judith,A; Zanko,Andrea; Korf,Bruce,R; Messiaen,Ludwine,M. "Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas." NATURE GENETICS. Vol. 46, no. 2. (February 2014.): 182-?.
"Chromosomal Abnormalities in Pregnancy: Case Reports." Presented at Mt. Sinai Medical Center OB/GYN Grand Rounds, . (March 1997)
"Cancer Genetic Counseling." Presented at Great Lakes Regional Genetics Group Annual Meeting, . (April 1997)
"Genetic Diseases in the Jewish Population." Presented at Temple Emanuel Monthly Meeting, . (March 1998)
"Genetic Testing and Insurance." Presented at The Jewish Community Federation Annual Meeting, . (June 1998)
"Genetic Testing for Breast Cancer: What It Means for You and Your Family.." Presented at Hadassah of Cleveland Quarterly Meeting, . (April 1999)
"The Genetics of Prostate Cancer." Presented at In Good Company: Prostate Cancer Support Group Monthly Meeting, . (July 2000)
"Cancer Genetic Counseling: Teaching Aids." Presented at Great Lakes Regional Genetics Group Annual Meeting, . (May 2000)
"The Genetics of Prostate Cancer." Presented at In Good Company: Prostate Cancer Support Group Monthly Meeting, . (March 2001)
"Impact of genetic discrimination on BRCA testing and medical management decisions.." Presented at American Society of Human Genetics Annual Meeting, . (January 2002)
"Novel Approach to Improved Access to Cancer Genetic Services: the Columbus, Ohio Solution.." Presented at American Society of Human Genetics Annual Meeting, . (January 2003)
"Low cancer incidence rates in Ohio Amish.." Presented at American Society of Human Genetics Annual Meeting, . (January 2003)
"An Update on Familial Non-Medullary Thyroid Cancer." Presented at National Society of Genetic Counselors Annual Education Conference, Los Angeles. (November 2005)
"Frequency of PTEN mutations in unselected cancer cohorts." Presented at National Society of Genetic Counselors Annual Education Conference, . (October 2008)
"Familial Papillary Thyroid Cancer." Presented at National Society of Genetic Counselors Annual Education Conference, . (October 2008)
"Familial non-medullary thyroid cancer." Presented at Annual thyroid cancer survivors (thyca.org) meeting, . (October 2010)
"Frequency of PTEN mutations in differentiated thyroid cancer.." Presented at International Thyroid Congress, . (September 2010)
"The genetics of neuroendocrine tumors: Who to refer and when to do testing." Presented at OSU Neuroendocrine tumor conference, . (December 2011)
"Cancer Genomics." Presented at NSGC 2011 Online Course, . (July 2011)
"Medullary thyroid carcinoma/MEN 2: Genetic counseling and follow-up." Presented at North American Neuroendocrine Tumor Society, . (October 2012)
|2007 - present||Editorial Board Member-Cancer genetics. National Cancer institute Physician Data Query (NCI PDQ).|
|2009 - present||Myriad Genetic Laboratories Advisory Board on Genetic Counseling: Alternative Service Delivery Models. Myriad Genetics Labs, Inc.. Salt lake City, UT.|
|2007 - 2009||Grant reviewer. National Society of Genetic Counselors.|
|2013||Expert content writer and speaker. GeneDx.|
Nagy R, Hicks M, Kloos J, Peay H, Westman R, Reiser C. Results of the Clinical Doctorate Survey: A report from the Genetic Counseling Advanced Degree Task Force.
Shen T, Teknos T, Toland A, Senter L, Nagy R.. Salivary gland cancer in BRCA positive families: a retrospective review. March 2014.
Tomsic J, He H, Akagi K, Liyanarachchi S, Pan Q, Bertani B, Symer DE, Nagy R, Blencowe BJ, de la Chapelle A. Exome sequencing identifies a rare mutation predisposing to papillary thyroid carcinoma.