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Items: 1 to 20 of 48

1.
CELSR2, Encoding a Planar Cell Polarity Protein, Is a Putative Gene in Joubert Syndrome with Cortical Heterotopia, Microophthalmia, and Growth Hormone Deficiency
Thierry Vilboux, May Christine V. Malicdan, Joseph C. Roney, Andrew R. Cullinane, Joshi Stephen, Deniz Yildirimli, Joy Bryant, Roxanne Fischer, Meghana Vemulapalli, James C. Mullikin, NISC Comparative Sequencing Program, Peter J. Steinbach, William A. Gahl, Meral Gunay-Aygun
Am J Med Genet A. Author manuscript; available in PMC 2020 Jun 17.
Published in final edited form as: Am J Med Genet A. 2017 Mar; 173(3): 661–666. Published online 2017 Jan 4. doi: 10.1002/ajmg.a.38005
PMCID:
PMC7299154
AbstractArticlePDF–673K
2.
Identification of CELSR2 as a novel prognostic biomarker for hepatocellular carcinoma
Mingxing Xu, Shu Zhu, Ruiyun Xu, Nan Lin
BMC Cancer. 2020; 20: 313. Published online 2020 Apr 15. doi: 10.1186/s12885-020-06813-5
PMCID:
PMC7161135
AbstractArticlePDF–4.3M
3.
CELSR2 is a candidate susceptibility gene in idiopathic scoliosis
Elisabet Einarsdottir, Anna Grauers, Jingwen Wang, Hong Jiao, Stefan A. Escher, Aina Danielsson, Ane Simony, Mikkel Andersen, Steen Bach Christensen, Kristina Åkesson, Ikuyo Kou, Anas M. Khanshour, Acke Ohlin, Carol Wise, Shiro Ikegawa, Juha Kere, Paul Gerdhem
PLoS One. 2017; 12(12): e0189591. Published online 2017 Dec 14. doi: 10.1371/journal.pone.0189591
PMCID:
PMC5730153
AbstractArticlePDF–4.4M
4.
Association of variants in CELSR2-PSRC1-SORT1 with risk of serum lipid traits, coronary artery disease and ischemic stroke
Yi-Jiang Zhou, Shao-Cai Hong, Qian Yang, Rui-Xing Yin, Xiao-Li Cao, Wu-Xian Chen
Int J Clin Exp Pathol. 2015; 8(8): 9543–9551. Published online 2015 Aug 1.
PMCID:
PMC4583949
AbstractArticlePDF–357K
5.
The adhesion GPCRs CELSR1–3 and LPHN3 engage G proteins via distinct activation mechanisms
Duy Lan Huong Bui, Andrew Roach, Jingxian Li, Sumit J. Bandekar, Elizabeth Orput, Ritika Raghavan, Demet Araç, Richard C. Sando
Cell Rep. Author manuscript; available in PMC 2023 Oct 23.
Published in final edited form as: Cell Rep. 2023 Jun 27; 42(6): 112552. Published online 2023 May 23. doi: 10.1016/j.celrep.2023.112552
PMCID:
PMC10592476
AbstractArticlePDF–4.9M
6.
Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma
Minerva M. Carrasquillo, Alexandra M. Nicholson, NiCole Finch, J. Raphael Gibbs, Matt Baker, Nicola J. Rutherford, Talisha A. Hunter, Mariely DeJesus-Hernandez, Gina D. Bisceglio, Ian R. Mackenzie, Andrew Singleton, Mark R. Cookson, Julia E. Crook, Allissa Dillman, Dena Hernandez, Ronald C. Petersen, Neill R. Graff-Radford, Steven G. Younkin, Rosa Rademakers
Am J Hum Genet. 2010 Dec 10; 87(6): 890–897. doi: 10.1016/j.ajhg.2010.11.002
PMCID:
PMC2997361
AbstractArticlePDF–569K
7.
LDL-cholesterol concentrations: a genome-wide association study
Manjinder S Sandhu, Dawn M Waterworth, Sally L Debenham, Eleanor Wheeler, Konstantinos Papadakis, Jing Hua Zhao, Kijoung Song, Xin Yuan, Toby Johnson, Sofie Ashford, Michael Inouye, Robert Luben, Matthew Sims, David Hadley, Wendy McArdle, Philip Barter, Y Antero Kesäniemi, Robert W Mahley, Ruth McPherson, Scott M Grundy, Wellcome Trust Case Control Consortium, Sheila A Bingham, Kay-Tee Khaw, Ruth JF Loos, Gérard Waeber, Inês Barroso, David P Strachan, Panagiotis Deloukas, Peter Vollenweider, Nicholas J Wareham, Vincent Mooser
Lancet. 2008 Feb 9; 371(9611): 483–491. doi: 10.1016/S0140-6736(08)60208-1
PMCID:
PMC2292820
AbstractArticle
8.
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies
Harald Grallert, Josée Dupuis, Joshua C. Bis, Abbas Dehghan, Maja Barbalic, Jens Baumert, Chen Lu, Nicholas L. Smith, André G. Uitterlinden, Robert Roberts, Natalie Khuseyinova, Renate B. Schnabel, Kenneth M. Rice, Fernando Rivadeneira, Ron C. Hoogeveen, João Daniel Fontes, Christa Meisinger, John F. Keaney, Jr., Rozenn Lemaitre, Yurii S. Aulchenko, Ramachandran S. Vasan, Stephen Ellis, Stanley L. Hazen, Cornelia M. van Duijn, Jeanenne J. Nelson, Winfried März, Heribert Schunkert, Ruth M. McPherson, Heide A. Stirnadel-Farrant, Bruce M. Psaty, Christian Gieger, David Siscovick, Albert Hofman, Thomas Illig, Mary Cushman, Jennifer F. Yamamoto, Jerome I. Rotter, Martin G. Larson, Alexandre F.R. Stewart, Eric Boerwinkle, Jacqueline C.M. Witteman, Russell P. Tracy, Wolfgang Koenig, Emelia J. Benjamin, Christie M. Ballantyne
Eur Heart J. 2012 Jan; 33(2): 238–251. Published online 2011 Oct 14. doi: 10.1093/eurheartj/ehr372
PMCID:
PMC3258449
AbstractArticlePDF–670K
9.
Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample
Matthew B. Lanktree, Sonia S. Anand, Salim Yusuf, Robert A. Hegele, the SHARE Investigators
J Lipid Res. 2009 Jul; 50(7): 1487–1496. doi: 10.1194/jlr.P900008-JLR200
PMCID:
PMC2694347
AbstractArticlePDF–1.4M
10.
Association of Blood Lipids with Common DNA Sequence Variants at Nineteen Genetic Loci in the Multiethnic United States National Health and Nutrition Examination Survey III
Mary E. Keebler, Christopher L. Sanders, Aarti Surti, Candace Guiducci, Noel P Burtt, Sekar Kathiresan
Circ Cardiovasc Genet. Author manuscript; available in PMC 2013 Feb 1.
Published in final edited form as: Circ Cardiovasc Genet. 2009 Jun; 2(3): 238–243. Published online 2009 Apr 14. doi: 10.1161/CIRCGENETICS.108.829473
PMCID:
PMC3561731
AbstractArticlePDF–233K
11.
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies
Muredach P Reilly, Mingyao Li, Jing He, Jane F Ferguson, Ioannis M Stylianou, Nehal N Mehta, Mary Susan Burnett, Joseph M Devaney, Christopher W Knouff, Prof John R Thompson, Benjamin D Horne, Alexandre F R Stewart, Themistocles L Assimes, Philipp S Wild, Hooman Allayee, Patrick Linsel Nitschke, Riyaz S Patel, Myocardial Infarction Genetics Consortium, Wellcome Trust Case Control Consortium, Nicola Martinelli, Prof Domenico Girelli, Prof Arshed A Quyyumi, Prof Jeffrey L Anderson, Prof Jeanette Erdmann, Alistair S Hall, Prof Heribert Schunkert, Prof Thomas Quertermous, Prof Stefan Blankenberg, Prof Stanley L Hazen, Prof Robert Roberts, Sekar Kathiresan, Prof Nilesh J Samani, Prof Stephen E Epstein, Prof Daniel J Rader
Lancet. Author manuscript; available in PMC 2012 Mar 8.
Published in final edited form as: Lancet. 2011 Jan 29; 377(9763): 383–392. Published online 2011 Jan 14. doi: 10.1016/S0140-6736(10)61996-4
PMCID:
PMC3297116
AbstractArticlePDF–2.2M
12.
Inactivating Celsr2 promotes motor axon fasciculation and regeneration in mouse and human
Quan Wen, Huandi Weng, Tao Liu, Lingtai Yu, Tianyun Zhao, Jingwen Qin, Si Li, Qingfeng Wu, Fadel Tissir, Yibo Qu, Libing Zhou
Brain. 2022 Feb; 145(2): 670–683. Published online 2022 Jan 4. doi: 10.1093/brain/awab317
PMCID:
PMC9014747
AbstractArticlePDF–2.3M
13.
Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham Heart Study data
Li Ma, Jing Yang, H Birali Runesha, Toshiko Tanaka, Luigi Ferrucci, Stefania Bandinelli, Yang Da
BMC Med Genet. 2010; 11: 55. Published online 2010 Apr 6. doi: 10.1186/1471-2350-11-55
PMCID:
PMC2867786
AbstractArticlePDF–1.0M
14.
Genome-Wide Association Study of Lp-PLA2 Activity and Mass in the Framingham Heart Study
Sunil Suchindran, David Rivedal, John R. Guyton, Tom Milledge, Xiaoyi Gao, Ashlee Benjamin, Jennifer Rowell, Geoffrey S. Ginsburg, Jeanette J. McCarthy
PLoS Genet. 2010 Apr; 6(4): e1000928. Published online 2010 Apr 29. doi: 10.1371/journal.pgen.1000928
PMCID:
PMC2861686
AbstractArticlePDF–969K
15.
Genome-wide Association Study Identifies Genes for Biomarkers of Cardiovascular Disease: Serum Urate and Dyslipidemia
Chris Wallace, Stephen J. Newhouse, Peter Braund, Feng Zhang, Martin Tobin, Mario Falchi, Kourosh Ahmadi, Richard J. Dobson, Ana Carolina B. Marçano, Cother Hajat, Paul Burton, Panagiotis Deloukas, Morris Brown, John M. Connell, Anna Dominiczak, G. Mark Lathrop, John Webster, The Wellcome Trust Case Control Consortium, Martin Farrall, Tim Spector, Nilesh J. Samani, Mark J. Caulfield, Patricia B. Munroe
Am J Hum Genet. 2008 Jan 10; 82(1): 139–149. Published online 2008 Jan 4. doi: 10.1016/j.ajhg.2007.11.001
PMCID:
PMC2253977
AbstractArticlePDF–507K
16.
Fine-Mapping in African Americans of Eight Recently Discovered Genetic Loci for Plasma Lipids: The Jackson Heart Study
Mary E. Keebler, Rahul C. Deo, Aarti Surti, David Konieczkowski, Candace Guiducci, Noel Burtt, Sarah G. Buxbaum, Daniel F. Sarpong, Michael W. Steffes, James G. Wilson, Herman A. Taylor, Sekar Kathiresan
Circ Cardiovasc Genet. Author manuscript; available in PMC 2011 Aug 1.
Published in final edited form as: Circ Cardiovasc Genet. 2010 Aug; 3(4): 358–364. Published online 2010 Jun 22. doi: 10.1161/CIRCGENETICS.109.914267
PMCID:
PMC3074173
AbstractArticlePDF–694K
17.
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos
Arthur Ko, Rita M. Cantor, Daphna Weissglas-Volkov, Elina Nikkola, Prasad M. V. Linga Reddy, Janet S. Sinsheimer, Bogdan Pasaniuc, Robert Brown, Marcus Alvarez, Alejandra Rodriguez, Rosario Rodriguez-Guillen, Ivette C. Bautista, Olimpia Arellano-Campos, Linda L. Muñoz-Hernández, Veikko Salomaa, Jaakko Kaprio, Antti Jula, Matti Jauhiainen, Markku Heliövaara, Olli Raitakari, Terho Lehtimäki, Johan G. Eriksson, Markus Perola, Kirk E. Lohmueller, Niina Matikainen, Marja-Riitta Taskinen, Maribel Rodriguez-Torres, Laura Riba, Teresa Tusie-Luna, Carlos A. Aguilar-Salinas, Päivi Pajukanta
Nat Commun. 2014 Jun 2; 5: 3983. Published online 2014 Jun 2. doi: 10.1038/ncomms4983
PMCID:
PMC4062071
AbstractArticlePDF–821K
18.
Joint Effects of Common Genetic Variants from Multiple Genes and Pathways On the Risk of Premature Coronary Artery Disease
Jeffrey L. Anderson, Benjamin D. Horne, Nicola J. Camp, Joseph B. Muhlestein, Paul N. Hopkins, Lisa A. Cannon-Albright, Chrissa P. Mower, James J. Park, Jessica L. Clarke, Zachary P. Nicholas, Jason T. McKinney, John F. Carlquist
Am Heart J. Author manuscript; available in PMC 2011 Aug 1.
Published in final edited form as: Am Heart J. 2010 Aug; 160(2): 250–256.e3. doi: 10.1016/j.ahj.2010.05.031
PMCID:
PMC2919893
AbstractArticlePDF–411K
19.
Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants
Myocardial Infarction Genetics Consortium
Nat Genet. Author manuscript; available in PMC 2009 Sep 1.
Published in final edited form as: Nat Genet. 2009 Mar; 41(3): 334–341. Published online 2009 Feb 8. doi: 10.1038/ng.327
Correction in:
volume 41 on page 762
PMCID:
PMC2681011
ArticlePDF–630K
20.
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
Samuli Ripatti, Emmi Tikkanen, Marju Orho-Melander, Aki S Havulinna, Kaisa Silander, Amitabh Sharma, Candace Guiducci, Markus Perola, Antti Jula, Juha Sinisalo, Marja-Liisa Lokki, Markku S Nieminen, Olle Melander, Veikko Salomaa, Leena Peltonen, Sekar Kathiresan
Lancet. 2010 Oct 23; 376(9750): 1393–1400. doi: 10.1016/S0140-6736(10)61267-6
PMCID:
PMC2965351
AbstractArticle

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