Zobrazeno 61 - 70
of 190
pro vyhledávání: '"Brendan J. Keating"'
Autor:
Sebastian Zöllner, Jared C. Roach, William Lawson, Howard J. Edenberg, Melvin G. McInnis, Dörthe Malzahn, Seth A. Ament, Sandra Meier, Heike Bickeböller, Jana Strohmaier, Peter Falkai, John R. Kelsoe, Evaristus A. Nwulia, William Byerley, Danjuma Quarless, Ney Alliey-Rodriguez, John I. Nurnberger, Paul D. Shilling, Marcella Rietschel, Stefanie Friedrichs, Monika Budde, Tatyana Shekhtman, Jens Treutlein, David Craig, Thomas G. Schulze, William Coryell, Judith A. Badner, Leroy Hood, Sarah S. Murray, Wade H. Berrettini, Peter P. Zandi, Chunyu Liu, Nicholas J. Schork, Erin N. Smith, Szabolcs Szelinger, Tiffany A. Greenwood, Tatiana Foroud, Markus M. Nöthen, Andreas J. Forstner, Francis J. McMahon, Elliot S. Gershon, Peng Zhang, Caroline M. Nievergelt, Maria Hipolito, Fabian Streit, Ashley L. Comes, Thomas W. Mühleisen, Daniel L. Koller, Franziska Degenhardt, Stephanie H. Witt, William A. Scheftner, Pamela B. Mahon, Cinnamon S. Bloss, Yiran Guo, John P. Rice, Sven Cichon, Brendan J. Keating, Josef Frank, Fernando S. Goes, James B. Potash
Publikováno v:
European Neuropsychopharmacology
European neuropsychopharmacology 29(1), 156-170 (2019). doi:10.1016/j.euroneuro.2018.10.005
Budde, M, Friedrichs, S, Alliey-Rodriguez, N, Ament, S, Badner, J A, Berrettini, W H, Bloss, C S, Byerley, W, Cichon, S, Comes, A L, Coryell, W, Craig, D W, Degenhardt, F, Edenberg, H J, Foroud, T, Forstner, A J, Frank, J, Gershon, E S, Goes, F S, Greenwood, T A, Guo, Y, Hipolito, M, Hood, L, Keating, B J, Koller, D L, Lawson, W B, Liu, C, Mahon, P B, McInnis, M G, McMahon, F J, Meier, S M, Mühleisen, T W, Murray, S S, Nievergelt, C M, Nurnberger, J I, Nwulia, E A, Potash, J B, Quarless, D, Rice, J, Roach, J C, Scheftner, W A, Schork, N J, Shekhtman, T, Shilling, P D, Smith, E N, Streit, F, Strohmaier, J, Szelinger, S, Treutlein, J, Witt, S H, Zandi, P P, Zhang, P, Zöllner, S, Bickeböller, H, Falkai, P G, Kelsoe, J R, Nöthen, M M, Rietschel, M, Schulze, T G & Malzahn, D 2019, ' Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder ', European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, vol. 29, no. 1, pp. 156-170 . https://doi.org/10.1016/j.euroneuro.2018.10.005
European neuropsychopharmacology 29(1), 156-170 (2019). doi:10.1016/j.euroneuro.2018.10.005
Budde, M, Friedrichs, S, Alliey-Rodriguez, N, Ament, S, Badner, J A, Berrettini, W H, Bloss, C S, Byerley, W, Cichon, S, Comes, A L, Coryell, W, Craig, D W, Degenhardt, F, Edenberg, H J, Foroud, T, Forstner, A J, Frank, J, Gershon, E S, Goes, F S, Greenwood, T A, Guo, Y, Hipolito, M, Hood, L, Keating, B J, Koller, D L, Lawson, W B, Liu, C, Mahon, P B, McInnis, M G, McMahon, F J, Meier, S M, Mühleisen, T W, Murray, S S, Nievergelt, C M, Nurnberger, J I, Nwulia, E A, Potash, J B, Quarless, D, Rice, J, Roach, J C, Scheftner, W A, Schork, N J, Shekhtman, T, Shilling, P D, Smith, E N, Streit, F, Strohmaier, J, Szelinger, S, Treutlein, J, Witt, S H, Zandi, P P, Zhang, P, Zöllner, S, Bickeböller, H, Falkai, P G, Kelsoe, J R, Nöthen, M M, Rietschel, M, Schulze, T G & Malzahn, D 2019, ' Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder ', European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, vol. 29, no. 1, pp. 156-170 . https://doi.org/10.1016/j.euroneuro.2018.10.005
Genome-wide association studies of case-control status have advanced the understanding of the genetic basis of psychiatric disorders. Further progress may be gained by increasing sample size but also by new analysis strategies that advance the exploi
Autor:
J. van Setten, R.A. de Weger, K.K. Kush, Michael V. Holmes, Folkert W. Asselbergs, Joseph W. Rossano, Pablo García-Pavía, O.C. Manintveld, N. de Jonge, Carla C. Baan, Brendan J. Keating, Jason H. Moore, Fernando Domínguez, Annemiek M.A. Peeters, B. Chang, Brian S. Cole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f96b91d5f60a5728ccc66d5f9861f5
https://www.webofscience.com/api/gateway?GWVersion=2SrcApp=PARTNER_APPSrcAuth=LinksAMRKeyUT=WOS:000430727300222DestLinkType=FullRecordDestApp=ALL_WOSUsrCustomerID=f41074198c063036414efcbc916f8956
https://www.webofscience.com/api/gateway?GWVersion=2SrcApp=PARTNER_APPSrcAuth=LinksAMRKeyUT=WOS:000430727300222DestLinkType=FullRecordDestApp=ALL_WOSUsrCustomerID=f41074198c063036414efcbc916f8956
Autor:
Brendan J. Keating, Rudaynah Al Ali, Cyril Cyrus, Hatem O. Qutub, Shahanas Chathoth, Brian Kim-Mozeleski, Chittibabu Vatte, Amein Al Ali, Yun Li, Abdullah M. Al-Rubaish, Samir H Al-Mueilo, Khaled R. Alkharsah, Fahad Al-Muhanna, Matthew B. Lanktree
Publikováno v:
BMC Nephrology
BMC Nephrology, Vol 19, Iss 1, Pp 1-6 (2018)
BMC Nephrology, Vol 19, Iss 1, Pp 1-6 (2018)
Background Genome wide association studies of patients with European descent have identified common variants associated with risk of reduced estimated glomerular filtration rate (eGFR). A panel of eight variants were selected to evaluate their associ
Autor:
Jenna Mancinelli, Brendan J. Keating, David Walls, Baoli Chang, Abraham Shaked, Maarouf Hoitet
Publikováno v:
Journal of Clinical and Translational Science
OBJECTIVES/SPECIFIC AIMS: Given the poor prognosis of HCC and its increasing incidence worldwide, identifying biomarkers of HCC has been an active area of research. While biomarkers are being identified at a rapid pace, many are still in early phases
Autor:
Kathryn J, Gray, Vesela P, Kovacheva, Hooman, Mirzakhani, Andrew C, Bjonnes, Berta, Almoguera, Andrew T, DeWan, Elizabeth W, Triche, Audrey F, Saftlas, Josephine, Hoh, Dale L, Bodian, Elisabeth, Klein, Kathi C, Huddleston, Sue Ann, Ingles, Charles J, Lockwood, Hakon, Hakonarson, Thomas F, McElrath, Jeffrey C, Murray, Melissa L, Wilson, Errol R, Norwitz, S Ananth, Karumanchi, Brian T, Bateman, Brendan J, Keating, Richa, Saxena
Publikováno v:
Hypertension (Dallas, Tex. : 1979). 72(2)
The genetic susceptibility to preeclampsia, a pregnancy-specific complication with significant maternal and fetal morbidity, has been poorly characterized. To identify maternal genes associated with preeclampsia risk, we assembled 498 cases and 1864
Publikováno v:
Transplant international : official journal of the European Society for Organ Transplantation. 31(3)
While advances in patient care and immunosuppressive pharmacotherapies have increased the lifespan of heart allograft recipients, there are still significant comorbidities post-transplantation and 5-year survival rates are still significant, at appro
Autor:
Brendan J. Keating, Jennifer G. Robinson, Kelli K. Ryckman, Josephine Hoh, Elizabeth W. Triche, Andrew Bjonnes, Patrick Breheny, Audrey F. Saftlas, Caitlin J. Smith, Andrew T. DeWan, Cassandra N. Spracklen, Richa Saxena
Publikováno v:
American Journal of Hypertension. 29:17-24
Background Preeclampsia is a hypertensive complication of pregnancy characterized by novel onset of hypertension after 20 weeks gestation, accompanied by proteinuria. Epidemiological evidence suggests that genetic susceptibility exists for preeclamps
Autor:
Mary E. Fischer, Barbara E.K. Klein, Ted S. Tweed, Karen J. Cruickshanks, Carla R. Schubert, Ronald Klein, Dayna S. Dalton, Guan-Hua Huang, David M. Nondahl, Brendan J. Keating
Publikováno v:
Atherosclerosis. 238:344-349
The study's purpose was to test if subclinical atherosclerosis was associated with the risk of developing HI in a large cohort of middle-aged participants.Study subjects were members of the Beaver Dam Offspring Study (BOSS), a longitudinal study of a
Autor:
Hakon Hakonarson, Juliana Teo, Yiran Guo, Xun Xu, Jiankang Li, Yulan Chen, Tatjana Kilo, Melissa Kartawinata, Tracy M. Bryan, Roger R. Reddel, Hilda A. Pickett, Lifeng Tian, Ahmad Al-Odaib, Brendan J. Keating, John Christodoulou, Pasquale M Barbaro
Publikováno v:
Blood. 124:2767-2774
Telomerase is a ribonucleoprotein enzyme that is necessary for overcoming telomere shortening in human germ and stem cells. Mutations in telomerase or other telomere-maintenance proteins can lead to diseases characterized by depletion of hematopoieti
Autor:
Yulan Chen, Robyn V. Jamieson, Loreto V. T. Rose, Sijie He, Lifeng Tian, Ivan Prokudin, Yiran Guo, Brendan J. Keating, Meredith Wilson, Xun Xu, Jinlong Liang, Hakon Hakonarson, Linda Goodwin, Dong Li
Publikováno v:
Clinical & Experimental Ophthalmology. 43:132-138
Background Several retinal dystrophies are associated with syndromic features including such conditions as Bardet–Biedl and Joubert syndromes. Cohen syndrome is an autosomal recessive disorder associated with multiple clinical manifestations includ