HuGE Literature Finder
Records 1-17
|
Whole-Exome Sequencing to Identify Rare Variants and Gene Networks that Increase Susceptibility to Scleroderma in African Americans.
Arthritis & rheumatology (Hoboken, N.J.) 2018 May . Gourh Pravitt, Remmers Elaine F, Boyden Steven E, Alexander Theresa, Morgan Nadia D, Shah Ami A, Mayes Maureen D, Doumatey Ayo, Bentley Amy R, Shriner Daniel, Domsic Robyn T, Medsger Thomas A, Steen Virginia D, Ramos Paula S, Silver Richard M, Korman Benjamin, Varga John, Schiopu Elena, Khanna Dinesh, Hsu Vivien, Gordon Jessica K, Saketkoo Lesley Ann, Gladue Heather, Kron Brynn, Criswell Lindsey A, Derk Chris T, Bridges S Louis, Shanmugam Victoria K, Kolstad Kathleen D, Chung Lorinda, Jan Reem, Bernstein Elana J, Goldberg Avram, Trojanowski Marcin, Kafaja Suzanne, Maksimowicz-McKinnon Kathleen M, Mullikin James C, , Adeyemo Adebowale, Rotimi Charles, Boin Francesco, Kastner Daniel L, Wigley Fredrick |
|
African genetic ancestry interacts with body mass index to modify risk for uterine fibroids.
PLoS genetics 2017 Jul 13 (7): e1006871. Giri Ayush, Edwards Todd L, Hartmann Katherine E, Torstenson Eric S, Wellons Melissa, Schreiner Pamela J, Velez Edwards Digna |
|
Whole Exome Sequencing for Identification of Potential Causal Variants for Diffuse Cutaneous Systemic Sclerosis.
Arthritis & rheumatology (Hoboken, N.J.) 2016 Apr . Mak Angel Cy, Tang Paul Lf, Cleveland Clare, Smith Melanie H, Connolly M Kari, Katsumoto Tamiko R, Wolters Paul J, Kwok Pui-Yan, Criswell Lindsey |
|
Copy number variation in patients with cervical artery dissection.
European journal of human genetics : EJHG 2012 Dec 20 (12): 1295-9. Grond-Ginsbach Caspar, Chen Bowang, Pjontek Rastislav, Wiest Tina, Jiang Yanxiang, Burwinkel Barbara, Tchatchou Sandrine, Krawczak Michael, Schreiber Stefan, Brandt Tobias, Kloss Manja, Arnold Marie-Luise, Hemminki Kari, Lichy Christoph, Lyrer Philippe A, Hausser Ingrid, Engelter Stefan |
|
Candidate gene analysis of spontaneous preterm delivery: new insights from re-analysis of a case-control study using case-parent triads and control-mother dyads.
BMC medical genetics 2011 12 (1): 174. Myking Solveig, Myhre Ronny, Gjessing Håkon K, Morken Nils-Halvdan, Sengpiel Verena, Williams Scott M, Ryckman Kelli K, Magnus Per, Jacobsson |
|
Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
|
A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM).
American journal of obstetrics and gynecology 2010 Oct 203 (4): 361.e1-361.e30. Romero Roberto, Friel Lara A, Velez Edwards Digna R, Kusanovic Juan Pedro, Hassan Sonia S, Mazaki-Tovi Shali, Vaisbuch Edi, Kim Chong Jai, Erez Offer, Chaiworapongsa Tinnakorn, Pearce Brad D, Bartlett Jacquelaine, Salisbury Benjamin A, Anant Madan Kumar, Vovis Gerald F, Lee Min Seob, Gomez Ricardo, Behnke Ernesto, Oyarzun Enrique, Tromp Gerard, Williams Scott M, Menon Ramkum |
|
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
|
Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes.
American journal of obstetrics and gynecology 2010 May 202 (5): 431.e1-34. Romero Roberto, Velez Edwards Digna R, Kusanovic Juan Pedro, Hassan Sonia S, Mazaki-Tovi Shali, Vaisbuch Edi, Kim Chong Jai, Chaiworapongsa Tinnakorn, Pearce Brad D, Friel Lara A, Bartlett Jacquelaine, Anant Madan Kumar, Salisbury Benjamin A, Vovis Gerald F, Lee Min Seob, Gomez Ricardo, Behnke Ernesto, Oyarzun Enrique, Tromp Gerard, Williams Scott M, Menon Ramkum |
|
Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth.
PloS one 2010 5 (2): e9040. Ryckman Kelli K, Morken Nils-Halvdan, White Marquitta J, Velez Digna R, Menon Ramkumar, Fortunato Stephen J, Magnus Per, Williams Scott M, Jacobsson |
|
Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
|
Associations of 25 structural, degradative, and inflammatory candidate genes with lumbar disc desiccation, bulging, and height narrowing.
Arthritis and rheumatism 2009 Feb 60 (2): 470-81. Videman Tapio, Saarela Janna, Kaprio Jaakko, Näkki Annu, Levälahti Esko, Gill Kevin, Peltonen Leena, Battié Michele |
|
Spontaneous preterm birth in African Americans is associated with infection and inflammatory response gene variants.
American journal of obstetrics and gynecology 2009 Feb 200 (2): 209.e1-27. Velez Digna R, Fortunato Stephen, Thorsen Poul, Lombardi Salvatore J, Williams Scott M, Menon Ramkum |
|
Racial disparity in pathophysiologic pathways of preterm birth based on genetic variants.
Reproductive biology and endocrinology : RB&E 2009 7 (1): 62. Menon Ramkumar, Pearce Brad, Velez Digna R, Merialdi Mario, Williams Scott M, Fortunato Stephen J, Thorsen Po |
|
Preterm birth in Caucasians is associated with coagulation and inflammation pathway gene variants.
PloS one 2008 3 (9): e3283. Velez Digna R, Fortunato Stephen J, Thorsen Poul, Lombardi Salvatore J, Williams Scott M, Menon Ramkum |
|
Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients.
Human genetics 2003 Dec 114 (1): 87-98. McCarthy Jeanette J, Meyer Joanne, Moliterno David J, Newby L Kristin, Rogers William J, Topol Eric J, |
|
Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Molecular medicine (Cambridge, Mass.) 0 16 (7-8): 247-53. Rose Jed E, Behm Frédérique M, Drgon Tomas, Johnson Catherine, Uhl George |
- Page last reviewed:Mar 16, 2019
- Page last updated:May 25, 2020
- Content source: