HuGE Literature Finder
Records 1-28
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The Effects of Single Nucleotide Polymorphisms in Korean Patients with Early-onset Atrial Fibrillation after Catheter Ablation.
Journal of Korean medical science 2020 Dec 35 (49): e411. Park Yae Min, Roh Seung Young, Lee Dae In, Shim Jaemin, Choi Jong Il, Park Sang Weon, Kim Young Ho |
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Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation.
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2019 Jun e12661. Seifert Mariam B, Olesen Morten S, Christophersen Ingrid E, Nielsen Jonas B, Carlson Jonas, Holmqvist Fredrik, Tveit Arnljot, Haunsø Stig, Svendsen Jesper H, Platonov Pyotr |
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PEX10, SIRPA-SIRPG, and SOX5 gene polymorphisms are strongly associated with nonobstructive azoospermia susceptibility.
Journal of assisted reproduction and genetics 2019 Mar . Gu Xiuli, Li Honggang, Chen Xi, Zhang Xue, Mei Fen, Jia Mingzhu, Xiong Chenglia |
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain.
PLoS genetics 2018 Sep 14 (9): e1007601. Suri Pradeep, Palmer Melody R, Tsepilov Yakov A, Freidin Maxim B, Boer Cindy G, Yau Michelle S, Evans Daniel S, Gelemanovic Andrea, Bartz Traci M, Nethander Maria, Arbeeva Liubov, Karssen Lennart, Neogi Tuhina, Campbell Archie, Mellstrom Dan, Ohlsson Claes, Marshall Lynn M, Orwoll Eric, Uitterlinden Andre, Rotter Jerome I, Lauc Gordan, Psaty Bruce M, Karlsson Magnus K, Lane Nancy E, Jarvik Gail P, Polasek Ozren, Hochberg Marc, Jordan Joanne M, Van Meurs Joyce B J, Jackson Rebecca, Nielson Carrie M, Mitchell Braxton D, Smith Blair H, Hayward Caroline, Smith Nicholas L, Aulchenko Yurii S, Williams Frances M |
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PR Interval Associated Genes, Atrial Remodeling and Rhythm Outcome of Catheter Ablation of Atrial Fibrillation-A Gene-Based Analysis of GWAS Data.
Frontiers in genetics 2017 8 224. Husser Daniela, Büttner Petra, Stübner Dorian, Ueberham Laura, Platonov Pyotr G, Dinov Borislav, Arya Arash, Hindricks Gerhard, Bollmann Andre |
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Silencing of the Drosophila ortholog of SOX5 leads to abnormal neuronal development and behavioral impairment.
Human molecular genetics 2017 04 26 (8): 1472-1482. Li Airong, Hooli Basavaraj, Mullin Kristina, Tate Rebecca E, Bubnys Adele, Kirchner Rory, Chapman Brad, Hofmann Oliver, Hide Winston, Tanzi Rudolph |
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Psoriasis risk SNPs and their association with HIV-1 control.
Human immunology 2016 Oct . Nititham Joanne, Gupta Rashmi, Zeng Xue, Hartogensis Wendy, Nixon Douglas F, Deeks Steven G, Hecht Frederick M, Liao Wils |
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Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.
Nature neuroscience 2016 Aug . Lelieveld Stefan H, Reijnders Margot R F, Pfundt Rolph, Yntema Helger G, Kamsteeg Erik-Jan, de Vries Petra, de Vries Bert B A, Willemsen Marjolein H, Kleefstra Tjitske, Löhner Katharina, Vreeburg Maaike, Stevens Servi J C, van der Burgt Ineke, Bongers Ernie M H F, Stegmann Alexander P A, Rump Patrick, Rinne Tuula, Nelen Marcel R, Veltman Joris A, Vissers Lisenka E L M, Brunner Han G, Gilissen Christi |
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Integrative analysis of genome-wide association studies and gene expression profiles identified candidate genes for osteoporosis in Kashin-Beck disease patients.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2015 Oct . Wen Y, Guo X, Hao J, Xiao X, Wang W, Wu C, Wang S, Yang T, Shen H, Chen X, Tan L, Tian Q, Deng H-W, Zhang |
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Genome-wide Loci linked to non-obstructive azoospermia susceptibility may be independent of reduced sperm production in males with normozoospermia.
Biology of reproduction 2015 Feb 92 (2): 41. Tu Wenling, Liu Yunqiang, Shen Ying, Yan Yuanlong, Wang Xianding, Yang Dong, Li Lei, Ma Yongxin, Tao Dachang, Zhang Sizhong, Yang Yu |
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Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study.
Journal of nutrigenetics and nutrigenomics 2015 8 (1): 44-53. Rudkowska Iwona, Pérusse Louis, Bellis Claire, Blangero John, Després Jean-Pierre, Bouchard Claude, Vohl Marie-Clau |
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A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation.
The American journal of cardiology 2014 Aug 114 (4): 593-600. Kolek Matthew J, Edwards Todd L, Muhammad Raafia, Balouch Adnan, Shoemaker M Benjamin, Blair Marcia A, Kor Kaylen C, Takahashi Atsushi, Kubo Michiaki, Roden Dan M, Tanaka Toshihiro, Darbar Dawo |
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The clinical and genetic features of COPD-asthma overlap syndrome.
The European respiratory journal 2014 Aug 44 (2): 341-50. Hardin Megan, Cho Michael, McDonald Merry-Lynn, Beaty Terri, Ramsdell Joe, Bhatt Surya, van Beek Edwin J R, Make Barry J, Crapo James D, Silverman Edwin K, Hersh Craig |
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Association study between polymorphisms of PRMT6, PEX10, SOX5, and nonobstructive azoospermia in the Han Chinese population.
Biology of reproduction 2014 May 90 (5): 96. Zou Shasha, Li Zheng, Wang Yanan, Chen Tingting, Song Pingping, Chen Jianhua, He Xiaojin, Xu Peng, Liang Ming, Luo Kailing, Zhu Xiaobin, Tian Erpo, Du Qiang, Wen Zujia, Li Zhiqiang, Wang Meng, Sha Yanwei, Cao Yunxia, Shi Yongyong, Hu Honglia |
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Whole-genome analysis in Korean patients with autoimmune myasthenia gravis.
Yonsei medical journal 2014 May 55 (3): 660-8. Na Sang-Jun, Lee Ji Hyun, Kim So Won, Kim Dae-Seong, Shon Eun Hee, Park Hyung Jun, Shin Ha Young, Kim Seung Min, Choi Young-Ch |
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Pathogenic variants screening in five non-obstructive azoospermia-associated genes.
Molecular human reproduction 2014 Feb 20 (2): 178-83. Lu Chuncheng, Xu Miaofei, Wang Rong, Qin Yufeng, Wang Ying, Wu Wei, Song Ling, Wang Shoulin, Shen Hongbing, Sha Jiahao, Miao Dengshun, Hu Zhibin, Xia Yankai, Wang Xin |
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Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia.
PloS one 2013 8 (1): e53042. Agim Zeynep Sena, Esendal Melda, Briollais Laurent, Uyan Ozgun, Meschian Mehran, Martinez Luis Antonio Mendoza, Ding Yongmei, Basak A Nazli, Ozcelik Hil |
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Evaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese population.
PloS one 2013 8 (11): e80374. Xu Miaofei, Qin Yufeng, Qu Jianhua, Lu Chuncheng, Wang Ying, Wu Wei, Song Ling, Wang Shoulin, Chen Feng, Shen Hongbing, Sha Jiahao, Hu Zhibin, Xia Yankai, Wang Xin |
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Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma.
Human genetics 2012 Sep 131 (9): 1507-17. Liu Yanhong, Melin Beatrice S, Rajaraman Preetha, Wang Zhaoming, Linet Martha, Shete Sanjay, Amos Christopher I, Lau Ching C, Scheurer Michael E, Tsavachidis Spiridon, Armstrong Georgina N, Houlston Richard S, Hosking Fay J, Claus Elizabeth B, Barnholtz-Sloan Jill, Lai Rose, Il'yasova Dora, Schildkraut Joellen, Sadetzki Siegal, Johansen Christoffer, Bernstein Jonine L, Olson Sara H, Jenkins Robert B, LaChance Daniel, Vick Nicholas A, Wrensch Margaret, Davis Faith, McCarthy Bridget J, Andersson Ulrika, Thompson Patricia A, Chanock Stephen, , Bondy Melissa |
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A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
Nature genetics 2011 Dec . Hu Z, Xia Y, Guo X, Dai J, Li H, Hu H, Jiang Y, Lu F, Wu Y, Yang X, Li H, Yao B, Lu C, Xiong C, Li Z, Gui Y, Liu J, Zhou Z, Shen H, Wang X, Sha J |
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Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
PLoS genetics 2011 Jul 7 (7): e1002178. Gorlova Olga, Martin Jose-Ezequiel, Rueda Blanca, Koeleman Bobby P C, Ying Jun, Teruel Maria, Diaz-Gallo Lina-Marcela, Broen Jasper C, Vonk Madelon C, Simeon Carmen P, Alizadeh Behrooz Z, Coenen Marieke J H, Voskuyl Alexandre E, Schuerwegh Annemie J, van Riel Piet L C M, Vanthuyne Marie, van 't Slot Ruben, Italiaander Annet, Ophoff Roel A, Hunzelmann Nicolas, Fonollosa Vicente, Ortego-Centeno Norberto, González-Gay Miguel A, García-Hernández Francisco J, González-Escribano María F, Airo Paolo, van Laar Jacob, Worthington Jane, Hesselstrand Roger, Smith Vanessa, de Keyser Filip, Houssiau Fredric, Chee Meng May, Madhok Rajan, Shiels Paul G, Westhovens Rene, Kreuter Alexander, de Baere Elfride, Witte Torsten, Padyukov Leonid, Nordin Annika, Scorza Raffaella, Lunardi Claudio, Lie Benedicte A, Hoffmann-Vold Anna-Maria, Palm Oyvind, García de la Peña Paloma, Carreira Patricia, , Varga John, Hinchcliff Monique, Lee Annette T, Gourh Pravitt, Amos Christopher I, Wigley Frederick M, Hummers Laura K, Nelson J Lee, Riemekasten Gabriella, Herrick Ariane, Beretta Lorenzo, Fonseca Carmen, Denton Christopher P, Gregersen Peter K, Agarwal Sandeep, Assassi Shervin, Tan Filemon K, Arnett Frank C, Radstake Timothy R D J, Mayes Maureen D, Martin Javi |
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Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs.
Molecular psychiatry 2011 Mar 16 (3): 321-32. Adkins D E, Aberg K, McClay J L, Bukszár J, Zhao Z, Jia P, Stroup T S, Perkins D, McEvoy J P, Lieberman J A, Sullivan P F, van den Oord E J C |
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A follow-up study for left ventricular mass on chromosome 12p11 identifies potential candidate genes.
BMC medical genetics 2011 12 (1): 100. Della-Morte David, Beecham Ashley, Rundek Tatjana, Wang Liyong, McClendon Mark S, Slifer Susan, Blanton Susan H, Di Tullio Marco R, Sacco Ralph |
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A functional RANKL polymorphism associated with younger age at onset of rheumatoid arthritis.
Arthritis and rheumatism 2010 Oct 62 (10): 2864-75. Tan Wenfeng, Wu Hui, Zhao Jian, Derber Lezlie A, Lee David M, Shadick Nancy A, Conn Doyt L, Smith Edwin A, Gersuk Vivian H, Nepom Gerald T, Moreland Larry W, Furst Daniel E, Thompson Susan D, Jonas Beth L, Holers V Michael, Glass David N, Chen Pojen P, Bridges S Louis, Weinblatt Michael E, Paulus Harold E, Tsao Betty |
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Genome-wide association analysis identifies multiple loci related to resting heart rate.
Human molecular genetics 2010 Oct 19 (19): 3885-94. Eijgelsheim Mark, Newton-Cheh Christopher, Sotoodehnia Nona, de Bakker Paul I W, Müller Martina, Morrison Alanna C, Smith Albert V, Isaacs Aaron, Sanna Serena, Dörr Marcus, Navarro Pau, Fuchsberger Christian, Nolte Ilja M, de Geus Eco J C, Estrada Karol, Hwang Shih-Jen, Bis Joshua C, Rückert Ina-Maria, Alonso Alvaro, Launer Lenore J, Hottenga Jouke Jan, Rivadeneira Fernando, Noseworthy Peter A, Rice Kenneth M, Perz Siegfried, Arking Dan E, Spector Tim D, Kors Jan A, Aulchenko Yurii S, Tarasov Kirill V, Homuth Georg, Wild Sarah H, Marroni Fabio, Gieger Christian, Licht Carmilla M, Prineas Ronald J, Hofman Albert, Rotter Jerome I, Hicks Andrew A, Ernst Florian, Najjar Samer S, Wright Alan F, Peters Annette, Fox Ervin R, Oostra Ben A, Kroemer Heyo K, Couper David, Völzke Henry, Campbell Harry, Meitinger Thomas, Uda Manuela, Witteman Jacqueline C M, Psaty Bruce M, Wichmann H-Erich, Harris Tamara B, Kääb Stefan, Siscovick David S, Jamshidi Yalda, Uitterlinden André G, Folsom Aaron R, Larson Martin G, Wilson James F, Penninx Brenda W, Snieder Harold, Pramstaller Peter P, van Duijn Cornelia M, Lakatta Edward G, Felix Stephan B, Gudnason Vilmundur, Pfeufer Arne, Heckbert Susan R, Stricker Bruno H Ch, Boerwinkle Eric, O'Donnell Christopher |
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Genome-wide association study of PR interval.
Nature genetics 2010 Feb 42 (2): 153-9. Pfeufer Arne, van Noord Charlotte, Marciante Kristin D, Arking Dan E, Larson Martin G, Smith Albert Vernon, Tarasov Kirill V, Müller Martina, Sotoodehnia Nona, Sinner Moritz F, Verwoert Germaine C, Li Man, Kao W H Linda, Köttgen Anna, Coresh Josef, Bis Joshua C, Psaty Bruce M, Rice Kenneth, Rotter Jerome I, Rivadeneira Fernando, Hofman Albert, Kors Jan A, Stricker Bruno H C, Uitterlinden André G, van Duijn Cornelia M, Beckmann Britt M, Sauter Wiebke, Gieger Christian, Lubitz Steven A, Newton-Cheh Christopher, Wang Thomas J, Magnani Jared W, Schnabel Renate B, Chung Mina K, Barnard John, Smith Jonathan D, Van Wagoner David R, Vasan Ramachandran S, Aspelund Thor, Eiriksdottir Gudny, Harris Tamara B, Launer Lenore J, Najjar Samer S, Lakatta Edward, Schlessinger David, Uda Manuela, Abecasis Gonçalo R, Müller-Myhsok Bertram, Ehret Georg B, Boerwinkle Eric, Chakravarti Aravinda, Soliman Elsayed Z, Lunetta Kathryn L, Perz Siegfried, Wichmann H-Erich, Meitinger Thomas, Levy Daniel, Gudnason Vilmundur, Ellinor Patrick T, Sanna Serena, Kääb Stefan, Witteman Jacqueline C M, Alonso Alvaro, Benjamin Emelia J, Heckbert Susan |
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Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).
The Journal of infectious diseases 2009 Oct 200 (8): 1194-201. Le Clerc Sigrid, Limou Sophie, Coulonges Cédric, Carpentier Wassila, Dina Christian, Taing Lieng, Delaneau Olivier, Labib Taoufik, Sladek Rob, , Deveau Christiane, Guillemain Hélène, Ratsimandresy Rojo, Montes Matthieu, Spadoni Jean-Louis, Therwath Amu, Schächter François, Matsuda Fumihiko, Gut Ivo, Lelièvre Jean-Daniel, Lévy Yves, Froguel Philippe, Delfraissy Jean-François, Hercberg Serge, Zagury Jean-Franço |
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Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years.
The Canadian journal of cardiology 0 28 (2): 191-5. Olesen Morten S, Holst Anders G, Jabbari Javad, Nielsen Jonas B, Christophersen Ingrid E, Sajadieh Ahmad, Haunsø Stig, Svendsen Jesper |
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- Page last updated:Feb 24, 2021
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