Power analysis for genome-wide association studies

por Klein, Robert J
Publicado 2007

RSEARCH: Finding homologs of single structured RNA sequences

por Klein, Robert J, Eddy, Sean R
Publicado 2003

Predicting functionally important SNP classes based on negative selection

por Levenstien, Mark A, Klein, Robert J
Publicado 2011

Are polygenic risk scores ready for the cancer clinic?—a perspective

por Klein, Robert J., Gümüş, Zeynep H.
Publicado 2022

Predicting acute suicidal ideation on Instagram using ensemble machine learning models

por Lekkas, Damien, Klein, Robert J., Jacobson, Nicholas C.
Publicado 2021

Anxiety, depression, and substance experimentation in childhood

por Klein, Robert J., Gyorda, Joseph A., Jacobson, Nicholas C.
Publicado 2022

Germline rare deleterious variant load alters cancer risk, age of onset and tumor characteristics

por Esai Selvan, Myvizhi, Onel, Kenan, Gnjatic, Sacha, Klein, Robert J., Gümüş, Zeynep H.
Publicado 2023

Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements

por Hayes, James E., Trynka, Gosia, Vijai, Joseph, Offit, Kenneth, Raychaudhuri, Soumya, Klein, Robert J.
Publicado 2015

Association of Selective Serotonin Reuptake Inhibitor Use With Abnormal Physical Movement Patterns as Detected Using a Piezoelectric Accelerometer and Deep Learning in a Nationally...

por Heinz, Michael V., Price, George D., Ruan, Franklin, Klein, Robert J., Nemesure, Matthew, Lopez, Aliza, Jacobson, Nicholas C.
Publicado 2022

Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk

por Willis, Jason A., Mukherjee, Semanti, Orlow, Irene, Viale, Agnes, Offit, Kenneth, Kurtz, Robert C., Olson, Sara H., Klein, Robert J.
Publicado 2014

Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding Variants within Complex-Trait Loci

por Trynka, Gosia, Westra, Harm-Jan, Slowikowski, Kamil, Hu, Xinli, Xu, Han, Stranger, Barbara E., Klein, Robert J., Han, Buhm, Raychaudhuri, Soumya
Publicado 2015

Prostate cancer polygenic risk score and prediction of lethal prostate cancer

por Klein, Robert J., Vertosick, Emily, Sjoberg, Dan, Ulmert, David, Rönn, Ann-Charlotte, Häggström, Christel, Thysell, Elin, Hallmans, Göran, Dahlin, Anders, Stattin, Pär, Melander, Olle, Vickers, Andrew, Lilja, Hans
Publicado 2022

ImmuneRegulation: a web-based tool for identifying human immune regulatory elements

por Kalayci, Selim, Selvan, Myvizhi Esai, Ramos, Irene, Cotsapas, Chris, Harris, Eva, Kim, Eun-Young, Montgomery, Ruth R, Poland, Gregory, Pulendran, Bali, Tsang, John S, Klein, Robert J, Gümüş, Zeynep H
Publicado 2019

MiXcan: a framework for cell-type-aware transcriptome-wide association studies with an application to breast cancer

por Song, Xiaoyu, Ji, Jiayi, Rothstein, Joseph H., Alexeeff, Stacey E., Sakoda, Lori C., Sistig, Adriana, Achacoso, Ninah, Jorgenson, Eric, Whittemore, Alice S., Klein, Robert J., Habel, Laurel A., Wang, Pei, Sieh, Weiva
Publicado 2023

Genetic markers of pigmentation are novel risk loci for uveal melanoma

por Ferguson, Robert, Vogelsang, Matjaz, Ucisik-Akkaya, Esma, Rai, Karan, Pilarski, Robert, Martinez, Carlos N., Rendleman, Justin, Kazlow, Esther, Nagdimov, Khagay, Osman, Iman, Klein, Robert J., Davidorf , Frederick H., Cebulla, Colleen M., Abdel-Rahman, Mohamed H., Kirchhoff , Tomas
Publicado 2016

Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genes

por Waller, Rosalie Griffin, Klein, Robert J, Vijai, Joseph, McKay, James D, Clay-Gilmour, Alyssa, Wei, Xiaomu, Madsen, Michael J, Sborov, Douglas W, Curtin, Karen, Slager, Susan L, Offit, Kenneth, Vachon, Celine M, Lipkin, Steven M, Dumontet, Charles, Camp, Nicola J
Publicado 2021

Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping

por Olshen, Adam B, Gold, Bert, Lohmueller, Kirk E, Struewing, Jeffery P, Satagopan, Jaya, Stefanov, Stefan A, Eskin, Eleazar, Kirchhoff, Tomas, Lautenberger, James A, Klein, Robert J, Friedman, Eitan, Norton, Larry, Ellis, Nathan A, Viale, Agnes, Lee, Catherine S, Borgen, Patrick I, Clark, Andrew G, Offit, Kenneth, Boyd, Jeff
Publicado 2008

Genetic Variation in DNA Repair Pathways and Risk of Non-Hodgkin's Lymphoma

por Rendleman, Justin, Antipin, Yevgeniy, Reva, Boris, Adaniel, Christina, Przybylo, Jennifer A., Dutra-Clarke, Ana, Hansen, Nichole, Heguy, Adriana, Huberman, Kety, Borsu, Laetitia, Paltiel, Ora, Ben-Yehuda, Dina, Brown, Jennifer R., Freedman, Arnold S., Sander, Chris, Zelenetz, Andrew, Klein, Robert J., Shao, Yongzhao, Lacher, Mortimer, Vijai, Joseph, Offit, Kenneth, Kirchhoff, Tomas
Publicado 2014

A Novel Genetic Variant in Long Non-coding RNA Gene NEXN-AS1 is Associated with Risk of Lung Cancer

por Yuan, Hua, Liu, Hongliang, Liu, Zhensheng, Owzar, Kouros, Han, Younghun, Su, Li, Wei, Yongyue, Hung, Rayjean J., McLaughlin, John, Brhane, Yonathan, Brennan, Paul, Bickeboeller, Heike, Rosenberger, Albert, Houlston, Richard S., Caporaso, Neil, Landi, Maria Teresa, Heinrich, Joachim, Risch, Angela, Christiani, David C., Gümüş, Zeynep H., Klein, Robert J., Amos, Christopher I., Wei, Qingyi
Publicado 2016

Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk

por Sieh, Weiva, Rothstein, Joseph H., Klein, Robert J., Alexeeff, Stacey E., Sakoda, Lori C., Jorgenson, Eric, McBride, Russell B., Graff, Rebecca E., McGuire, Valerie, Achacoso, Ninah, Acton, Luana, Liang, Rhea Y., Lipson, Jafi A., Rubin, Daniel L., Yaffe, Martin J., Easton, Douglas F., Schaefer, Catherine, Risch, Neil, Whittemore, Alice S., Habel, Laurel A.
Publicado 2020