Journal Articles
Courtright, P; Green, R; Pilarski, R; Smucny, J. "A survey of the eye complications of leprosy in South Korea.." Leprosy review. Vol. 55, no. 3. (January 1984.): 229-237
Pilarski, R, T; Pauli, R, M; Engber, W D. "Hand-reduction malformations: genetic and syndromic analysis.." Journal of pediatric orthopedics. Vol. 5, no. 3. (January 1985.): 274-280
Pilarski, R, T; Pauli, R, M; Bresnick, G, H; Lebovitz, R M. "Karsch-Neugebauer syndrome: split foot/split hand and congenital nystagmus.." Clinical genetics. Vol. 27, no. 1. (January 1985.): 97-101
Pilarski, R, T; Greenstein, R, M; Benn, P. "Developing a role for genetics within a cancer program.." Annals of the New York Academy of Sciences. Vol. 768, (January 1995.)
Shattuck-Eidens, D; Oliphant, A; McClure, M; McBride, C; Gupte, J; Rubano, T; Pruss, D; Tavtigian, S, V; Teng, D, H; Adey, N; Staebell, M; Gumpper, K; Lundstrom, R; Hulick, M; Kelly, M; Holmen, J; Lingenfelter, B; Manley, S; Fujimura, F; Luce, M; et al.. "BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing." JAMA : the journal of the American Medical Association. Vol. 278, no. 15. (January 1997.): 1242-1250
Pilarski, R; Greenstein, R M. "Cancer gene testing?." Connecticut medicine. Vol. 62, no. 4. (January 1998.): 248-?
Pilarski, R, T; Brothman, A, R; Benn, P; Shulman Rosengren, S. "Attenuated familial adenomatous polyposis in a man with an interstitial deletion of chromosome arm 5q." American journal of medical genetics. Vol. 86, no. 4. (January 1999.): 321-324
Zhou, X, P; Woodford-Richens, K; Lehtonen, R; Kurose, K; Aldred, M; Hampel, H; Launonen, V; Virta, S; Pilarski, R; Salovaara, R; Bodmer, W, F; Conrad, B, A; Dunlop, M; Hodgson, S, V; Iwama, T; Jarvinen, H; Kellokumpu, I; Kim, J, C; Leggett, B; Markie, D; et al.. "Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.." American journal of human genetics. Vol. 69, no. 4. (January 2001.): 704-711
Zhou, Xiao-Ping; Waite, Kristin, A; Pilarski, Robert; Hampel, Heather; Fernandez, Magali, J; Bos, Cindy; Dasouki, Majed; Feldman, Gerald, L; Greenberg, Lois, A; Ivanovich, Jennifer; Matloff, Ellen; Patterson, Annette; Pierpont, Mary Ella; Russo, Donna; Nassif, Najah, T; Eng, Charis. "Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway.." American journal of human genetics. Vol. 73, no. 2. (January 2003.): 404-411
Pilarski, R; Eng, C. "Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome.." Journal of Medical Genetics. Vol. 41, no. 5. (January 2004.)
McWhinney, Sarah, R; Pilarski, Robert, T; Forrester, Shawnia, R; Schneider, Michael, C; Sarquis, M Marta; Dias, Eduardo, P; Eng, Charis. "Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma.." The Journal of clinical endocrinology and metabolism. Vol. 89, no. 11. (January 2004.): 5694-5699
Oktenli, Cagatay; Gul, Davut; Deveci, M Salih; Saglam, Mutlu; Upadhyaya, Meena; Thompson, Peter; Consoli, Claudia; Kocar, Ismail, H; Pilarski, Robert; Zhou, Xiao-Ping; Eng, Charis. "Unusual features in a patient with neurofibromatosis type 1: multiple subcutaneous lipomas, a juvenile polyp in ascending colon, congenital intrahepatic portosystemic venous shunt, and horseshoe kidney.." American journal of medical genetics. Part A. Vol. 127, no. 3. (January 2004.): 298-301
Agrawal, Shipra; Pilarski, Robert; Eng, Charis. "Different splicing defects lead to differential effects downstream of the lipid and protein phosphatase activities of PTEN.." Human molecular genetics. Vol. 14, no. 16. (January 2005.): 2459-2468
Butler, M, G; Dasouki, M, J; Zhou, X-P; Talebizadeh, Z; Brown, M; Takahashi, T, N; Miles, J, H; Wang, C, H; Stratton, R; Pilarski, R; Eng, C. "Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.." Journal of medical genetics. Vol. 42, no. 4. (January 2005.): 318-321
Sweet, Kevin; Willis, Joseph; Zhou, Xiao-Ping; Gallione, Carol; Sawada, Takeshi; Alhopuro, Pia; Khoo, Sok Kean; Patocs, Attila; Martin, Cossette; Bridgeman, Scott; Heinz, John; Pilarski, Robert; Lehtonen, Rainer; Prior, Thomas, W; Frebourg, Thierry; Teh, Bin Tean; Marchuk, Douglas, A; Aaltonen, Lauri, A; Eng, Charis. "Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.." JAMA : the journal of the American Medical Association. Vol. 294, no. 19. (January 2005.): 2465-2473
Pyatt, Robert, E; Pilarski, Robert; Prior, Thomas W. "Mutation screening in juvenile polyposis syndrome.." The Journal of molecular diagnostics : JMD. Vol. 8, no. 1. (January 2006.): 84-88
Tekin,Mustafa; Hismi,Burcu,Oztürk; Fitoz,Suat; Yalçinkaya,Fatos; Ekim,Mesiha; Kansu,Aydan; Ertem,Mehmet; Deda,Gülhis; Tutar,Ercan; Arsan,Saadet; Zhou,Xiao-Ping; Pilarski,Robert; Eng,Charis; Akar,Nejat. "A germline PTEN mutation with manifestations of prenatal onset and verrucous epidermal nevus.." American journal of medical genetics. Part A. Vol. 140, no. 13. (July 2006.): 1472-1475
Tekin, Mustafa; Hismi, Burcu Ozturk; Fitoz, Suat; Yalcinkaya, Fatos; Ekim, Mesiha; Kansu, Aydan; Ertem, Mehmet; Deda, Gulhis; Tutar, Ercan; Arsan, Saadet; Zhou, Xiao-Ping; Pilarski, Robert; Eng, Charis; Akar, Nejat. "A germline PTEN mutation with manifestations of prenatal onset and verrucous epidermal nevus.." American journal of medical genetics. Part A. Vol. 140, no. 13. (January 2006.): 1472-1475
Sarquis, Marta, S; Agrawal, Shipra; Shen, Lei; Pilarski, Robert; Zhou, Xiao-Ping; Eng, Charis. "Distinct expression profiles for PTEN transcript and its splice variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome." American journal of human genetics. Vol. 79, no. 1. (January 2006.): 23-30
Pezzolesi, Marcus, G; Li, Yan; Zhou, Xiao-Ping; Pilarski, Robert; Shen, Lei; Eng, Charis. "Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.." American journal of human genetics. Vol. 79, no. 5. (January 2006.): 923-934
Pilarski, Robert. "Risk perception among women at risk for hereditary breast and ovarian cancer.." Journal of Genetic Counseling. Vol. 18, no. 4. (January 2009.): 303-312
Pilarski, Robert. "Cowden syndrome: a critical review of the clinical literature.." Journal of Genetic Counseling. Vol. 18, no. 1. (January 2009.): 13-27
Ginsburg OM, Akbari MR, Aziz Z, Young R, Lynch H, Ghadirian P, Robidoux A, Londono J, Vasquez G, Gomes M, Costa MM, Dimitrakakis C, Gutierrez G, Pilarski R, Royer R, Narod SA. "The prevalence of germ-line TP53 mutations in women diagnosed with breast cancer before age 30.." Familial Cancer. Vol. 8, (January 2009.): 563-567
Young, SR, Pilarski RT, Donenberg, T, Shapiro, C, Hammond, LS, Miller, J, Brooks, KA, Cohen, S, Tenenholz, B, DeSai, D, Zandvakili, I, Royer, R, Li, S and Narod, SA. "The prevalence of BRCA mutations among young women with triple negative breast cancer.." BMC Cancer. Vol. 9, (January 2009.): 86-90
Guler, G, Huebner, K, Himmetoglu, C, Jimenez, R.E., Costinean, S, Volinia, S, Pilarski, RT, Hayran, M, Shapiro?, CL.. "Fragile histidine triad protein, WW domain-containing oxidoreductase protein Wwox, and activator protein 2γ expression levels correlate with basal phenotype in breast cancer.." Cancer. Vol. 115, no. 4. (January 2009.): 899-908
Sweet K, Senter L, Pilarski R, Wei L, Toland AW. "Characterization of BRCA1 ring finger variants of uncertain significance.." Breast Cancer Res Treat. Vol. 119, no. 3. (January 2010.): 737-743
Abdel-Rahman, MH, Pilarski, R, Ezzat, S, Sexton, J, and Davidorf, FH. "Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma.." Familial Cancer. Vol. 9, (August 2010.): 431-438
Abdel-Rahman, MH, Pilarski, R.. "Hereditary predisposition rather than environmental factors are likely to explain the familial link between uveal melanoma and other cancers.." Familial Cancer. Vol. 9, (January 2010.): 661-662
Westman, JA, Ferketich, AK, Kauffman, RM, MacEachern, SN, Wilkins III, JR, Wilcox, PP, Pilarski, RT, Nagy, R, Lemeshow, S, de la Chapelle, A, Bloomfield, CD.. "Low cancer incidence rates in Ohio Amish.." Cancer Causes and Control. Vol. 21, no. 1. (January 2010.): 69-75
Daly MB, Axilbund JE, Buys S, Crawford B, Farrell CD, Friedman S, Garber JE, Goorha S, Gruber SB, Hampel H, Kaklamani V, Kohlmann W, Kurian A, Litton J, Marcom PK, Nussbaum R, Offit K, Pal T, Pasche B, Pilarski R, Reiser G, Shannon KM, Smith JR, Swisher E, Weitzel JN.. "Genetic/familial high-risk assessment: breast and ovarian.." J Natl Compr Canc Netw. Vol. 8, no. 5. (January 2010.): 562-594
Abdel-Rahman MH, Pilarski R, Cebulla CM, Massengill J, Christopher B, Hovland P, Davidorf FH.. "Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma and other cancers.." Journal of Medical Genetics. Vol. 48, no. 12. (December 2011.): 856-859
Kais,Zeina; Barsky,Sanford,H; Mathsyaraja,Haritha; Zha,Alicia; Ransburgh,Derek,JR; He,Gang; Pilarski,Robert,T; Shapiro,Charles,L; Huang,Kun; Parvin,Jeffrey,D. "KIAA0101 Interacts with BRCA1 and Regulates Centrosome Number." Molecular Cancer Research. Vol. 9, no. 8. (August 2011.): 1091-1099
Guler,Gulnur; Himmetoglu,Cigdem; Jimenez,Rafael,E; Geyer,Susan,M; Wang,Wenle,P; Costinean,Stefan; Pilarski,Robert,T; Morrison,Carl; Suren,Dinc; Liu,Jianhua; Chen,Jingchun; Kamal,Jyoti; Shapiro,Charles,L; Huebner,Kay. "Aberrant expression of DNA damage response proteins is associated with breast cancer subtype and clinical features." BREAST CANCER RESEARCH AND TREATMENT. Vol. 129, no. 2. (September 2011.): 421-432
Abdel-Rahman,Mohamed,H; Pilarski,Robert; Massengill,James,B; Christopher,Benjamin,B; Davidorf,Frederick,H. "Lack of GNAQ germline mutations in uveal melanoma patients with high risk for hereditary cancer predisposition." Familial Cancer. Vol. 10, no. 2. (June 2011.): 319-321
Abdel-Rahman,Mohamed,H; Pilarski,Robert; Massengill,James,B; Christopher,Benjamin,N; Noss,Ryan; Davidorf,Frederick,H. "Melanoma candidate genes CDKN2A/p16/INK4A, p14ARF, and CDK4 sequencing in patients with uveal melanoma with relative high-risk for hereditary cancer predisposition." Melanoma Research. Vol. 21, no. 3. (June 2011.): 175-179
Pilarski,Robert; Stephens,Julie,A; Noss,Ryan; Fisher,James,L; Prior,Thomas,W. "Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features." Journal of Medical Genetics. Vol. 48, no. 8. (August 2011.): 505-512
Pilarski,Robert; Nagy,Rebecca. "Genetic Testing by Cancer Site: Endocrine System." CANCER JOURNAL. Vol. 18, no. 4. (July 2012.): 364-371
Daniels,Molly,S; Rich,Thereasa; Weissman,Scott; Pilarski,Robert. "Lifetime Cancer Risks of PTEN Mutation Carriers-Letter." CLINICAL CANCER RESEARCH. Vol. 18, no. 15. (August 2012.): 4213-4213
Pilarski,Robert; Patel,Divya,A; Weitzel,Jeffrey; McVeigh,Terri; Dorairaj,Jemima,J; Heneghan,Helen,M; Miller,Nicola; Weidhaas,Joanne,B; Kerin,Michael,J; McKenna,Megan; Wu,Xifeng; Hildebrandt,Michelle; Zelterman,Daniel; Sand,Sharon; Shulman,Lee,P. "The KRAS-Variant Is Associated with Risk of Developing Double Primary Breast and Ovarian Cancer." PLOS ONE. Vol. 7, no. 5. (May 2012.): e37891
Gammon,A; Jasperson,K; Pilarski,R; Prior,T,W; Kuwada,S. "PTEN mosaicism with features of Cowden syndrome." CLINICAL GENETICS. Vol. 84, no. 6. (December 2013.): 593-595
Pilarski,Robert; Burt,Randall; Kohlman,Wendy; Pho,Lana; Shannon,Kristen,M; Swisher,Elizabeth. "Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria." JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE. Vol. 105, no. 21. (November 2013.): 1607-1616
Meyer,Kerstin,B; O'Reilly,Martin; Michailidou,Kyriaki; Carlebur,Saskia; Edwards,Stacey,L; French,Juliet,D; Prathalingham,Radhika; Dennis,Joe; Bolla,Manjeet,K; Wang,Qin; de Santiago,Ines; Hopper,John,L; Tsimiklis,Helen; Apicella,Carmel; Southey,Melissa,C; Schmidt,Marjanka,K; Broeks,Annegien; van't Veer,Laura,J; Hogervorst,Frans,B; Muir,Kenneth; Lophatananon,Artitaya; Stewart-Brown,Sarah; Siriwanarangsan,Pornthep; Fasching,Peter,A; Lux,Michael,P; Ekici,Arif,B; Beckmann,Matthias,W; Peto,Julian; Silva,Isabel,dos Santos; Fletcher,Olivia; Johnson,Nichola; Sawyer,Elinor,J; Tomlinson,Ian; Kerin,Michael,J; Miller,Nicola; Marme,Federick; Schneeweiss,Andreas; Sohn,Christof; Burwinkel,Barbara; Guenel,Pascal; Truong,Therese; Laurent-Puig,Pierre; Menegaux,Florence; Bojesen,Stig,E; Nordestgaard,Borge,G; Nielsen,Sune,F; Flyger,Henrik; Milne,Roger,L; Pilar Zamora,M; Arias,Jose,I; Benitez,Javier; Neuhausen,Susan; Anton-Culver,Hoda; Ziogas,Argyrios; Dur,Christina,C; Brenner,Hermann; Mueller,Heiko; Arndt,Volker; Stegmaier,Christa; Meindl,Alfons; Schmutzler,Rita,K; Engel,Christoph; Ditsch,Nina; Brauch,Hiltrud; Bruening,Thomas; Ko,Yon-Dschun; Nevanlinna,Heli; Muranen,Taru,A; Aittomaeki,Kristiina; Blomqvist,Carl; Matsuo,Keitaro; Ito,Hidemi; Iwata,Hiroji; Yatabe,Yasushi; Doerk,Thilo; Helbig,Sonja; Bogdanova,Natalia,V; Lindblom,Annika; Margolin,Sara; Mannermaa,Arto; Kataja,Vesa; Kosma,Veli-Matti; Hartikainen,Jaana,M; Chenevix-Trench,Georgia; Wu,Anna,H; Tseng,Chiu-Chen; Van Den Berg,David; Stram,Daniel,O; Lambrechts,Diether; Thienpont,Bernard; Christiaens,Marie-Rose; Smeets,Ann; Chang-Claude,Jenny; Rudolph,Anja; Seibold,Petra; Flesch-Janys,Dieter; Radice,Paolo; Peterlongo,Paolo; Bonanni,Bernardo; Bernard,Loris; Couch,Fergus,J; Olson,Janet,E; Wang,Xianshu; Purrington,Kristen; Giles,Graham,G; Severi,Gianluca; Baglietto,Laura; McLean,Catriona; Haiman,Christopher,A; Henderson,Brian,E; Schumacher,Fredrick; Le Marchand,Loic; Simard,Jacques; Goldberg,Mark,S; Labreche,France; Dumont,Martine; Teo,So. "Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1." AMERICAN JOURNAL OF HUMAN GENETICS. Vol. 93, no. 6. (December 2013.): 1046-1060
Garcia-Closas,Montserrat; Couch,Fergus,J; Lindstrom,Sara et al.. "Genome-wide association studies identify four ER negative-specific breast cancer risk loci." NATURE GENETICS. Vol. 45, no. 4. (April 2013.): 392-398
Jin,Ming; Hampel,Heather; Pilarski,Robert; Zhou,Xiaoping; Peters,Sara; Frankel,Wendy,L. "Phosphatase and Tensin Homolog Immunohistochemical Staining and Clinical Criteria for Cowden Syndrome in Patients With Trichilemmoma or Associated Lesions." AMERICAN JOURNAL OF DERMATOPATHOLOGY. Vol. 35, no. 6. (August 2013.): 637-640
Stanich,Peter,P; Meyer,Marty,M; Pilarski,Robert. "Correspondence regarding: PTEN hamartoma tumor syndromes in childhood: Description of two cases and a proposal for follow-up protocol." AMERICAN JOURNAL OF MEDICAL GENETICS PART A. Vol. 164, no. 7. (July 2014.): 1870-1870
Purrington,Kristen,S; Slager,Susan; Eccles,Diana; Yannoukakos,Drakoulis; Fasching,Peter,A; Miron,Penelope; Carpenter,Jane; Chang-Claude,Jenny; Martin,Nicholas,G; Montgomery,Grant,W; Kristensen,Vessela; Anton-Culver,Hoda; Goodfellow,Paul; Tapper,William,J; Rafiq,Sajjad; Gerty,Susan,M; Durcan,Lorraine; Konstantopoulou,Irene; Fostira,Florentia; Vratimos,Athanassios; Apostolou,Paraskevi; Konstanta,Irene; Kotoula,Vassiliki; Lakis,Sotiris; Dimopoulos,Meletios,A; Skarlos,Dimosthenis; Pectasides,Dimitrios; Fountzilas,George; Beckmann,Matthias,W; Hein,Alexander; Ruebner,Matthias; Ekici,Arif,B; Hartmann,Arndt; Schulz-Wendtland,Ruediger; Renner,Stefan,P; Janni,Wolfgang; Rack,Brigitte; Scholz,Christoph; Neugebauer,Julia; Andergassen,Ulrich; Lux,Michael,P; Haeberle,Lothar; Clarke,Christine; Pathmanathan,Nirmala; Rudolph,Anja; Flesch-Janys,Dieter; Nickels,Stefan; Olson,Janet,E; Ingle,James,N; Olswold,Curtis; Slettedahl,Seth; Eckel-Passow,Jeanette,E; Anderson,S,Keith; Visscher,Daniel,W; Cafourek,Victoria,L; Sicotte,Hugues; Prodduturi,Naresh; Weiderpass,Elisabete; Bernstein,Leslie; Ziogas,Argyrios; Ivanovich,Jennifer; Giles,Graham,G; Baglietto,Laura; Southey,Melissa; Kosma,Veli-Matti; Fischer,Hans-Peter; Reed,Malcom,WR; Cross,Simon,S; Deming-Halverson,Sandra; Shrubsole,Martha; Cai,Qiuyin; Shu,Xiao-Ou; Daly,Mary; Weaver,JoEllen; Ross,Eric; Klemp,Jennifer; Sharma,Priyanka; Torres,Diana; Rudiger,Thomas; Wolfing,Heidrun; Ulmer,Hans-Ulrich; Forsti,Asta; Khoury,Thaer; Kumar,Shicha; Pilarski,Robert; Shapiro,Charles,L; Greco,Dario; Heikkila,Paivi; Aittomaki,Kristiina; Blomqvist,Carl; Irwanto,Astrid; Liu,Jianjun; Pankratz,Vernon,Shane; Wang,Xianshu; Severi,Gianluca; Mannermaa,Arto; Easton,Douglas; Hall,Per; Brauch,Hiltrud; Cox,Angela; Zheng,Wei; Godwin,Andrew,K; Hamann,Ute; Ambrosone,Christine; Toland,Amanda,Ewart; Nevanlinna,Heli; Vachon,Celine,M; Couch,Fergus,J. "Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer." CARCINOGENESIS. Vol. 35, no. 5. (May 2014.): 1012-1019
Pilarski,Robert; Burt,Randall; Kohlman,Wendy; Pho,Lana; Shannon,Kristen,M; Swisher,Elizabeth. "RE: Cowden Syndrome and PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria Response." JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE. Vol. 106, no. 6. (June 2014.): dju131
Stanich,Peter,P; Pilarski,Robert; Rock,Jonathan; Frankel,Wendy,L; El-Dika,Samer; Meyer,Marty,M. "Colonic manifestations of PTEN hamartoma tumor syndrome: Case series and systematic review." WORLD JOURNAL OF GASTROENTEROLOGY. Vol. 20, no. 7. (February 2014.): 1833-1838
Stanich,Peter,P; Meyer,Marty,M; Pilarski,Robert. "Correspondence regarding: PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol.." American journal of medical genetics. Part A. Vol. 164A, no. 7. (July 2014.): 1870-?
Hall,Michael,J; Forman,Andrea,D; Pilarski,Robert; Wiesner,Georgia; Giri,Veda,N. "Gene Panel Testing for Inherited Cancer Risk." JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK. Vol. 12, no. 9. (September 2014.): 1339-1346
Daly,Mary,B; Pilarski,Robert; Axilbund,Jennifer,E; Buys,Saundra,S; Crawford,Beth; Friedman,Susan; Garber,Judy,E; Horton,Carolyn; Kaklamani,Virginia; Klein,Catherine; Kohlmann,Wendy; Kurian,Allison; Litton,Jennifer; Madlensky,Lisa; Marcom,P,Kelly; Merajver,Sofia,D; Offit,Kenneth; Pal,Tuya; Pasche,Boris; Reiser,Gwen; Shannon,Kristen,Mahoney; Swisher,Elizabeth; Voian,Nicoleta,C; Weitzel,Jeffrey,N; Whelan,Alison; Wiesner,Georgia,L; Dwyer,Mary,A; Kumar,Rashmi. "Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 1.2014." JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK. Vol. 12, no. 9. (September 2014.): 1326-1338
Pilarski, RT. "Genetics of PTEN Hamartoma Tumour Syndrome." eLS. Vol. 1, (July 2014.)
King-Spohn, K; Pilarski, RT. "Beyond BRCA1 and BRCA2." Current Problems in Cancer. Vol. 38, no. 6. (November 2014.): 235-248
Pilarski,Robert; Cebulla,Colleen,M; Massengill,James,B; Rai,Karan; Rich,Thereasa; Strong,Louise; McGillivray,Barbara; Asrat,Mary-Jill; Davidorf,Frederick,H; Abdel-Rahman,Mohamed,H. "Expanding the Clinical Phenotype of Hereditary BAP1 Cancer Predisposition Syndrome, Reporting Three New Cases." GENES CHROMOSOMES & CANCER. Vol. 53, no. 2. (February 2014.): 177-182
Reinbolt, R; Patel, R; Pan, X; et al.. "Risk factors for anthracycline-associated cardiotoxicity." Supportive Care in Cancer. Vol. ePub, (November 2015.): 1-7
McVeigh,Terri,P; Jung,Song-Yi; Kerin,Michael,J; Salzman,David,W; Nallur,Sunitha; Nemec,Antonio,A; Dookwah,Michelle; Sadofsky,Jackie; Paranjape,Trupti; Kelly,Olivia; Chan,Elcie; Miller,Nicola; Sweeney,Karl,J; Zelterman,Daniel; Sweasy,Joann; Pilarski,Robert; Telesca,Donatello; Slack,Frank,J; Weidhaas,Joanne,B. "Estrogen withdrawal, increased breast cancer risk and the KRAS-variant." CELL CYCLE. Vol. 14, no. 13. (July 2015.): 2091-2099
Cebulla,Colleen,M; Binkley,Elaine,M; Pilarski,Robert; Massengill,James,B; Rai,Karan; Liebner,David,A; Marino,Meghan,J; Singh,Arun,D; Abdel-Rahman,Mohamed,H. "Analysis of BAP1 Germline Gene Mutation in Young Uveal Melanoma Patients." OPHTHALMIC GENETICS. Vol. 36, no. 2. (June 2015.): 126-131
Briercheck,Edward,L; Trotta,Rossana; Chen,Li; Hartlage,Alex,S; Cole,Jordan,P; Cole,Tyler,D; Mao,Charlene; Banerjee,Pinaki,P; Hsu,Hsiang-Ting; Mace,Emily,M; Ciarlariello,David; Mundy-Bosse,Bethany,L; Garcia-Cao,Isabel; Scoville,Steven,D; Yu,Lianbo; Pilarski,Robert; Carson,William,E; Leone,Gustavo; Pandolfi,Pier,Paolo; Yu,Jianhua; Orange,Jordan,S; Caligiuri,Michael,A. "PTEN Is a Negative Regulator of NK Cell Cytolytic Function." JOURNAL OF IMMUNOLOGY. Vol. 194, no. 4. (February 2015.): 1832-1840
Rai, K; Pilarski, RT; Cebulla, CM; Abdel-Rahman, MH. "Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases." Clinical Genetics. Vol. [Epub ahead of print], (June 2015.)
Caserta, E; Egriboz, O; Wang, H; et al.. "Non-catalytic PTEN missense mutation predisposes to organ-selective cancer development in vivo." Genes and Development. Vol. 29, (August 2015.): 1707-1720
Couch,Fergus,J; Hart,Steven,N; Sharma,Priyanka; Toland,Amanda,Ewart; Wang,Xianshu; Miron,Penelope; Olson,Janet,E; Godwin,Andrew,K; Pankratz,V,Shane; Olswold,Curtis; Slettedahl,Seth; Hallberg,Emily; Guidugli,Lucia; Davila,Jaime,I; Beckmann,Matthias,W; Janni,Wolfgang; Rack,Brigitte; Ekici,Arif,B; Slamon,Dennis,J; Konstantopoulou,Irene; Fostira,Florentia; Vratimos,Athanassios; Fountzilas,George; Pelttari,Liisa,M; Tapper,William,J; Durcan,Lorraine; Cross,Simon,S; Pilarski,Robert; Shapiro,Charles,L; Klemp,Jennifer; Yao,Song; Garber,Judy; Cox,Angela; Brauch,Hiltrud; Ambrosone,Christine; Nevanlinna,Heli; Yannoukakos,Drakoulis; Slager,Susan,L; Vachon,Celine,M; Eccles,Diana,M; Fasching,Peter,A. "Inherited Mutations in 17 Breast Cancer Susceptibility Genes Among a Large Triple-Negative Breast Cancer Cohort Unselected for Family History of Breast Cancer." JOURNAL OF CLINICAL ONCOLOGY. Vol. 33, no. 4. (February 2015.): 304-U154
Abdel-Rahman, M; Rai, K; Pilarski, R; et al.. "Germline BAP1 mutations misreported as somatic based on tumor-only testing." Familial Cancer. Vol. ePub, (January 2016.): 1-4
Daly, MB; Pilarski, R; Axilbund, J; et al.. "Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015. Featured Updates to the NCCN Guidelines." Journal of the National Comprehensive Cancer Network. Vol. 14, no. 2. (February 2016.): 153-162