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Alison Patricia Klein, M.H.S., Ph.D.
Professor of Oncology
Research Interests: Genetic Epidemiology; Pancreatic Cancer; Risk assessment; Familial Cancer Syndromes; Inherited cancer susceptibility
Dr. Klein is a Professor of Oncology, Pathology and Epidemiology and a trained genetic epidemiologist/statistical geneticist. She has studied the genetic epidemiology of pancreatic cancer for over 17 years. Her research has focused on the discovery of pancreatic cancer susceptibility genes, using linkage, sequencing and association approaches as well as quantification of pancreatic cancer risk due to familial and genetic factors. As part of this work, she has identified rare variants in PALB2 and ATM are associated with familial pancreatic cancer, as well as lead the Pancreatic Cancer Case Control Consortium Genome-Wide association studies of pancreatic cancer (NCI RO1/CIDR supported).
Dr. Klein is Director of the National Familial Pancreas Tumor Registry, the largest single-site registry of familial pancreatic cancer in the world. Currently, over 6,500 families have enrolled in this registry including over 1,700 with familial pancreatic cancer (i.e., defined as a kindred with at least a pair of first-degree relatives with pancreatic cancer). In addition, she is co-leader of the Familial Pancreatic Cancer Genome Sequencing Project conducted within the PACGENE consortium where we have recently completed whole genome sequencing analysis of 638 patients with familial pancreatic cancer. She is also the PI of a NCI/CIDR supported multi-center GWAS for pancreatic cancer and PI of the Johns Hopkins SPORE in Gastrointestinal cancer. She is a founding member of the Pancreatic Cancer Case-Control Consortium and member of the SU2C Pancreatic Cancer Interception Dream Team.
- Professor of Oncology
- Professor of Pathology
- B.S., Boston College (Massachusetts) (1994)
- M.H.S., Johns Hopkins Bloomberg School of Public Health (Maryland) (1999)
- Ph.D., Johns Hopkins Bloomberg School of Public Health (Maryland) (2001)
Research & Publications
Dr. Klein is the Director of the National Familial Pancreas Tumor Registry, the largest pancreatic cancer family registry in the world (www.nfptr.org). She is a genetic epidemiologist with a focus on cancer research. Her current work focuses on the identification the genetic and environmental risk factors for pancreatic cancer as well as other complex genetic diseases. Recently, in the first demonstration that whole exome sequencing approaches can be used to identify the causes of a hereditary disease, she discovered that mutations in the PALB2 gene increase the risk of pancreatic cancer. In addition, she has developed a clinical risk assessment tool for high-risk pancreatic cancer families, PancPRO in order to facilitate the translation of her research findings into the clinical setting.
Jones S, Hruban RH, Kamiyama M, Borges M, Zhang X, Parsons DW, Lin JC, Palmisano E, Brune K, Jaffee EM, Iacobuzio-Donahue CA, Maitra A, Parmigiani G, Kern SE, Velculescu VE, Kinzler KW, Vogelstein B, Eshleman JR*, Goggins M*, Klein AP*. Exomic Sequencing Identifies PALB2 as a Pancreatic Cancer Susceptibility Gene. Science. 2009 Apr 10;324(5924):217. Epub 2009 Mar 5.
Roberts NJ, Jiao Y, Yu J, Kopelovich L, Petersen GM, Bondy ML, Gallinger S, Schwartz AG, Syngal S, Cote ML, Axilbund J, Schulick R, Ali SZ, Eshleman JR, Velculescu VE, Goggins M, Vogelstein B, Papadopoulos N, Hruban RH, Kinzler, KW, Klein AP. ATM Mutations in Patients with Hereditary Pancreatic Cancer. Cancer Discovery 2012(2)41
Roberts NJ, Norris AL, Petersen GM, Bondy ML Brand R, Gallinger S, Kurtz R, Olson SH, Rustgi AN, Schwartz A, Stoffel E, Syngal S, Zogopoulos G, Ali SZ, Axilbund J, Chaffee K, Chen YC, Cote ML, Childs EJ, Douville C, Goes FS, Herman JM, Iacobuzio-Donahue C, Kramer M, Makohon-Moore A, McCombie RW, McMahon, KW, Niknafs N, Parla J, Pirooznia, Potash J, Rhim AD, Smith AL, Wang Y, Wolfgang CL, Wood LD, Zandi PP, Goggins MG, Karchin R, Eshleman JR, Papadopoulos N, Kinzler KW, Vogelstein B, Hruban RH, Klein AP. Cancer Discov. 2016 Feb;6(2):166-75. doi: 10.1158/2159-8290.CD-15-0402. Epub 2015 Dec 9. PubMed PMID: 26658419; PubMed Central PMCID: PMC4744563.
Childs EJ*, Mocci E*, Campa D*, Bracci PM, Gallinger S, Goggins M, Li D, Neale R, Olson SH, Scelo G, Amundadottir LT, Bamlet WR, Bijlsma MF, Blackford A, Borges M, Brennan P11, Brenner H, Bueno-de-Mesquita HB, Canzian F, Capurso G, Cavestro GM, Chaffee KG, Chanock SJ12, Cleary SP, Cotterchio M, Foretova L, Fuchs C, Funel N, Gazouli M, Hassan M, Herman JM, Holcatova I, Holly EA, Hoover RN, Hung RJ, Janout V, Key TJ, Kupcinskas J, Kurtz RC, Landi S, Lu L, Malecka-Panas E, Mambrini A, Mohelnikova-Duchonova B, Neoptolemos JP, Oberg AL, Orlow I, Pasquali C, Pezzilli R, Rizzato C, Saldia A, Scarpa A, Stolzenberg-Solomon RZ, Strobel O, Tavano F, Vashist YK, Vodicka P, Wolpin BM, Yu H, Petersen GM, Risch HA, Klein AP Common variation at at 17q25.1, 3q29, 7p13, and 2p13.3 associated with susceptibility of pancreatic cancer. Nature Genetics,
Wang W, Chen S, Hruban RH, Parmigiani G, Klein AP. PancPRO:risk assessment for individuals with a family history of pancreatic cancer. JCO 2007 Apr 10;25(11): 1417-1422