Genome-wide association study link novel loci to endometriosis von Albertsen, Hans M, Chettier, Rakesh, Farrington, Pamela, Ward, Kenneth

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A protein interaction network of the malaria parasite Plasmodium falciparum von LaCount, Douglas J., Vignali, Marissa, Chettier, Rakesh, Phansalkar, Amit, Bell, Russell, Hesselberth, Jay R., Schoenfeld, Lori W., Ota, Irene, Sahasrabudhe, Sudhir, Kurschner, Cornelia, Fields, Stanley, Hughes, Robert E.

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Endometriosis is associated with rare copy number variants von Chettier, Rakesh, Ward, Kenneth, Albertsen, Hans M

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Huntingtin interacting proteins are genetic modifiers of neurodegeneration von Kaltenbach, Linda S, Romero, Eliana, Becklin, Robert R, Chettier, Rakesh, Bell, Russell, Phansalkar, Amit, Strand, Andrew, Torcassi, Cameron, Savage, Justin, Hurlburt, Anthony, Cha, Guang-Ho, Ukani, Lubna, Chepanoske, Cindy Lou, Zhen, Yuejun, Sahasrabudhe, Sudhir, Olson, James, Kurschner, Cornelia, Ellerby, Lisa M, Peltier, John M, Botas, Juan, Hughes, Robert E

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Haplotypes at LBX1 have distinct inheritance patterns with opposite effects in adolescent idiopathic scoliosis von Chettier, Rakesh, Nelson, Lesa, Ogilvie, James W, Albertsen, Hans M, Ward, Kenneth

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Validation of DNA-based prognostic testing to predict spinal curve progression in adolescent idiopathic scoliosis von Ward, Kenneth, Ogilvie, James W, Singleton, Marc V, Chettier, Rakesh, Engler, Gordon, Nelson, Lesa M

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Polygenic inheritance of adolescent idiopathic scoliosis: A study of extended families in Utah von Ward, Kenneth, Ogilvie, James, Argyle, VeeAnn, Nelson, Lesa, Meade, Mary, Braun, John, Chettier, Rakesh

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A human protein interaction network shows conservation of aging processes between human and invertebrate species von Bell, Russell, Hubbard, Alan, Chettier, Rakesh, Chen, Di, Miller, John P, Kapahi, Pankaj, Tarnopolsky, Mark, Sahasrabuhde, Sudhir, Melov, Simon, Hughes, Robert E

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Endometriosis risk allele in Wnt4 may interact with rare mutations in HDAC2 gene von Ward, Kenneth, Chettier, Rakesh, Albertsen, Hans M.

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Cytoskeletal and extra cellular matrix genes are key contributors in the pathogenesis of endometriosis von Albertsen, Hans M., Chettier, Rakesh, Ward, Kenneth

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Interaction of an atypical Plasmodium falciparum ETRAMP with human apolipoproteins von Vignali, Marissa, McKinlay, Anastasia, LaCount, Douglas J, Chettier, Rakesh, Bell, Russell, Sahasrabudhe, Sudhir, Hughes, Robert E, Fields, Stanley

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Cardiomyopathy and Preeclampsia: Shared Genetics? von Gammill, Hilary S., Chettier, Rakesh, Brewer, Alina, Roberts, James M., Shree, Raj, Tsigas, Eleni, Ward, Kenneth

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COPY NUMBER LOSSES IN SPECIFIC REGIONS OF COMMON VARIATION ARE SIGNIFICANTLY MORE PREVALENT IN INFERTILITY PATIENTS COMPARED WITH A POPULATION OF DEMONSTRATED FERTILITY AND LOW FET... von Wassman, Edward Robert, Chettier, Rakesh, Nelson, Lesa M., Serrano, Moises A., Zdunich, Dane, Ward, Kenneth

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Synthetic-lethal interactions between ATR inhibition and functional genetic and proteomic biomarkers to predict responses in endometriosis-associated cancers von Gilad, Oren, Li, Dansu, George, Erin, Chettier, Rakesh, Simpkins, Fiona, Ward, Kenneth, Brown, Eric J

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Somatic cancer driver mutations in endometriosis lesions contribute to secondary cancer risk von Ward, Kenneth, Chettier, Rakesh, Albertsen, Hans M., Morgan, Terry, Williams, Todd

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Cardiomyopathy and Preeclampsia von Gammill, Hilary S, Chettier, Rakesh, Brewer, Alina, Roberts, James M, Shree, Raj, Tsigas, Eleni, Ward, Kenneth

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Whole exome sequencing identifies hemizygous deletions in the UGT2B28 and USP17L2 genes in a three‑generation family with endometriosis von Albertsen, Hans M, Matalliotaki, Charoula, Matalliotakis, Michail, Zervou, Maria I, Matalliotakis, Ioannis, Spandidos, Demetrios A, Chettier, Rakesh, Ward, Kenneth, Goulielmos, George N

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Co-existence of endometriosis with 13 non-gynecological co-morbidities: Mutation analysis by whole exome sequencing von Matalliotaki, Charoula, Matalliotakis, Michail, Zervou, Maria I, Trivli, Alexandra, Matalliotakis, Ioannis, Mavromatidis, George, Spandidos, Demetrios A, Albertsen, Hans M, Chettier, Rakesh, Ward, Kenneth, Goulielmos, George N

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Progesterone Receptor Genotype, Family History, and Spontaneous Preterm Birth von Manuck, Tracy A., Major, Heather D., Varner, Michael W., Chettier, Rakesh, Nelson, Lesa, Esplin, M. Sean

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723: Genome-wide association study of preeclampsia points to several novel genes von Ward, Kenneth, Chettier, Rakesh, Ward, Jeff, Nelson, Lesa

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