HuGE Literature Finder
Records 1-30
The Genetic Makeup of the Electrocardiogram.
Cell systems 2020 Sep 11 (3): 229-238.e5. Verweij Niek, Benjamins Jan-Walter, Morley Michael P, van de Vegte Yordi J, Teumer Alexander, Trenkwalder Teresa, Reinhard Wibke, Cappola Thomas P, van der Harst P |
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Insights into malaria susceptibility using genome-wide data on 17,000 individuals from Africa, Asia and Oceania.
Nature communications 2019 12 10 (1): 5732. Authors are not available |
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Pharmacogenetic assessment of tafenoquine efficacy in patients with Plasmodium vivax malaria.
Pharmacogenetics and genomics 2020 09 30 (7): 161-165. St Jean Pamela L, Koh Gavin C K W, Breton John J, Espino Fe E J, Hien Tran T, Krudsood Srivicha, Lacerda Marcus V G, Llanos-Cuentas Alejandro, Lon Chanthap, Mohammed Rezika, Namaik-Larp Chayadol S, Pereira Dhelio B, Saunders David L, Velez Ivan D, Yilma Daniel, Villegas Maria F, Duparc Stephan, Green Justin |
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Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance.
Blood advances 2020 Jun 4 (12): 2789-2797. Clay-Gilmour Alyssa I, Hildebrandt Michelle A T, Brown Elizabeth E, Hofmann Jonathan N, Spinelli John J, Giles Graham G, Cozen Wendy, Bhatti Parveen, Wu Xifeng, Waller Rosalie G, Belachew Alem A, Robinson Dennis P, Norman Aaron D, Sinnwell Jason P, Berndt Sonja I, Rajkumar S Vincent, Kumar Shaji K, Chanock Stephen J, Machiela Mitchell J, Milne Roger L, Slager Susan L, Camp Nicola J, Ziv Elad, Vachon Celine |
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Genome-wide association study identifies genetic susceptibility loci and pathways of radiation-induced acute oral mucositis.
Journal of translational medicine 2020 06 18 (1): 224. Yang Da-Wei, Wang Tong-Min, Zhang Jiang-Bo, Li Xi-Zhao, He Yong-Qiao, Xiao Ruowen, Xue Wen-Qiong, Zheng Xiao-Hui, Zhang Pei-Fen, Zhang Shao-Dan, Hu Ye-Zhu, Shen Guo-Ping, Chen Mingyuan, Sun Ying, Jia Wei-H |
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Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction.
Nature communications 2020 09 11 (1): 4432. Saw Jacqueline, Yang Min-Lee, Trinder Mark, Tcheandjieu Catherine, Xu Chang, Starovoytov Andrew, Birt Isabelle, Mathis Michael R, Hunker Kristina L, Schmidt Ellen M, Jackson Linda, Fendrikova-Mahlay Natalia, Zawistowski Matthew, Brummett Chad M, Zoellner Sebastian, Katz Alexander, Coleman Dawn M, Swan Kirby, O'Donnell Christopher J, , Zhou Xiang, Li Jun Z, Gornik Heather L, Assimes Themistocles L, Stanley James C, Brunham Liam R, Ganesh Santhi |
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Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.
The Lancet. Neurology 2020 10 19 (10): 840-848. Jones Emma, Hummerich Holger, Viré Emmanuelle, Uphill James, Dimitriadis Athanasios, Speedy Helen, Campbell Tracy, Norsworthy Penny, Quinn Liam, Whitfield Jerome, Linehan Jacqueline, Jaunmuktane Zane, Brandner Sebastian, Jat Parmjit, Nihat Akin, How Mok Tze, Ahmed Parvin, Collins Steven, Stehmann Christiane, Sarros Shannon, Kovacs Gabor G, Geschwind Michael D, Golubjatnikov Aili, Frontzek Karl, Budka Herbert, Aguzzi Adriano, Karamujic-Comic Hata, van der Lee Sven J, Ibrahim-Verbaas Carla A, van Duijn Cornelia M, Sikorska Beata, Golanska Ewa, Liberski Pawel P, Calero Miguel, Calero Olga, Sanchez-Juan Pascual, Salas Antonio, Martinón-Torres Federico, Bouaziz-Amar Elodie, Haïk Stéphane, Laplanche Jean-Louis, Brandel Jean-Phillipe, Amouyel Phillipe, Lambert Jean-Charles, Parchi Piero, Bartoletti-Stella Anna, Capellari Sabina, Poleggi Anna, Ladogana Anna, Pocchiari Maurizio, Aneli Serena, Matullo Giuseppe, Knight Richard, Zafar Saima, Zerr Inga, Booth Stephanie, Coulthart Michael B, Jansen Gerard H, Glisic Katie, Blevins Janis, Gambetti Pierluigi, Safar Jiri, Appleby Brian, Collinge John, Mead Sim |
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Genetic Association Analyses Highlight
Circulation. Genomic and precision medicine 2019 10 12 (10): e002617. Thériault Sébastien, Dina Christian, Messika-Zeitoun David, Le Scouarnec Solena, Capoulade Romain, Gaudreault Nathalie, Rigade Sidwell, Li Zhonglin, Simonet Floriane, Lamontagne Maxime, Clavel Marie-Annick, Arsenault Benoit J, Boureau Anne-Sophie, Lecointe Simon, Baron Estelle, Bonnaud Stéphanie, Karakachoff Matilde, Charpentier Eric, Fellah Imen, Roussel Jean-Christian, Philippe Verhoye Jean, Baufreton Christophe, Probst Vincent, Roussel Ronan, , Redon Richard, Dagenais François, Pibarot Philippe, Mathieu Patrick, Le Tourneau Thierry, Bossé Yohan, Schott Jean-Jacqu |
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The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.
Nature communications 2020 03 11 (1): 1600. Xie Jingyuan, Liu Lili, Mladkova Nikol, Li Yifu, Ren Hong, Wang Weiming, Cui Zhao, Lin Li, Hu Xiaofan, Yu Xialian, Xu Jing, Liu Gang, Caliskan Yasar, Sidore Carlo, Balderes Olivia, Rosen Raphael J, Bodria Monica, Zanoni Francesca, Zhang Jun Y, Krithivasan Priya, Mehl Karla, Marasa Maddalena, Khan Atlas, Ozay Fatih, Canetta Pietro A, Bomback Andrew S, Appel Gerald B, Sanna-Cherchi Simone, Sampson Matthew G, Mariani Laura H, Perkowska-Ptasinska Agnieszka, Durlik Magdalena, Mucha Krzysztof, Moszczuk Barbara, Foroncewicz Bartosz, Paczek Leszek, Habura Ireneusz, Ars Elisabet, Ballarin Jose, Mani Laila-Yasmin, Vogt Bruno, Ozturk Savas, Yildiz Abdülmecit, Seyahi Nurhan, Arikan Hakki, Koc Mehmet, Basturk Taner, Karahan Gonca, Akgul Sebahat Usta, Sever Mehmet Sukru, Zhang Dan, Santoro Domenico, Bonomini Mario, Londrino Francesco, Gesualdo Loreto, Reiterova Jana, Tesar Vladimir, Izzi Claudia, Savoldi Silvana, Spotti Donatella, Marcantoni Carmelita, Messa Piergiorgio, Galliani Marco, Roccatello Dario, Granata Simona, Zaza Gianluigi, Lugani Francesca, Ghiggeri GianMarco, Pisani Isabella, Allegri Landino, Sprangers Ben, Park Jin-Ho, Cho BeLong, Kim Yon Su, Kim Dong Ki, Suzuki Hitoshi, Amoroso Antonio, Cattran Daniel C, Fervenza Fernando C, Pani Antonello, Hamilton Patrick, Harris Shelly, Gupta Sanjana, Cheshire Chris, Dufek Stephanie, Issler Naomi, Pepper Ruth J, Connolly John, Powis Stephen, Bockenhauer Detlef, Stanescu Horia C, Ashman Neil, Loos Ruth J F, Kenny Eimear E, Wuttke Matthias, Eckardt Kai-Uwe, Köttgen Anna, Hofstra Julia M, Coenen Marieke J H, Kiemeney Lambertus A, Akilesh Shreeram, Kretzler Matthias, Beck Lawrence H, Stengel Benedicte, Debiec Hanna, Ronco Pierre, Wetzels Jack F M, Zoledziewska Magdalena, Cucca Francesco, Ionita-Laza Iuliana, Lee Hajeong, Hoxha Elion, Stahl Rolf A K, Brenchley Paul, Scolari Francesco, Zhao Ming-Hui, Gharavi Ali G, Kleta Robert, Chen Nan, Kiryluk Krzyszt |
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A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness.
Communications biology 2020 Jun 3 (1): 301. Choquet Hélène, Melles Ronald B, Yin Jie, Hoffmann Thomas J, Thai Khanh K, Kvale Mark N, Banda Yambazi, Hardcastle Alison J, Tuft Stephen J, Glymour M Maria, Schaefer Catherine, Risch Neil, Nair K Saidas, Hysi Pirro G, Jorgenson Er |
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Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian-randomization study.
International journal of epidemiology 2020 May . Dardani Christina, Howe Laurence J, Mukhopadhyay Nandita, Stergiakouli Evie, Wren Yvonne, Humphries Kerry, Davies Amy, Ho Karen, Weinberg Seth M, Marazita Mary L, Mangold Elisabeth, Ludwig Kerstin U, Relton Caroline L, Davey Smith George, Lewis Sarah J, Sandy Jonathan, Davies Neil M, Sharp Gemma |
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Genomewide Association Study of Acute Anterior Uveitis Identifies New Susceptibility Loci.
Investigative ophthalmology & visual science 2020 Jun 61 (6): 3. Huang Xiu-Feng, Li Zhixiu, De Guzman Erika, Robinson Philip, Gensler Lianne, Ward Michael M, Rahbar Mohammad Hossein, Lee MinJae, Weisman Michael H, Macfarlane Gary J, Jones Gareth T, Klingberg Eva, Forsblad-d'Elia Helena, McCluskey Peter, Wakefield Denis, Coombes Jeff S, Fiatarone Singh Maria A, Mavros Yorgi, Vlahovich Nicole, Hughes David C, Marzo-Ortega Helena, Van der Horste-Bruinsma Irene, O'Shea Finbar, Martin Tammy M, Rosenbaum James, Breban Maxime, Jin Zi-Bing, Leo Paul, Reveille John D, Wordsworth B Paul, Brown Matthew |
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Genome-Wide Association Meta-Analysis of Single-Nucleotide Polymorphisms and Symptomatic Venous Thromboembolism during Therapy for Acute Lymphoblastic Leukemia and Lymphoma in Caucasian Children.
Cancers 2020 May 12 (5): . Mateos Marion K, Tulstrup Morten, Quinn Michael Cj, Tuckuviene Ruta, Marshall Glenn M, Gupta Ramneek, Mayoh Chelsea, Wolthers Benjamin O, Barbaro Pasquale M, Ruud Ellen, Sutton Rosemary, Huttunen Pasi, Revesz Tamas, Trakymiene Sonata S, Barbaric Draga, Tedgård Ulf, Giles Jodie E, Alvaro Frank, Jonsson Olafur G, Mechinaud Françoise, Saks Kadri, Catchpoole Daniel, Kotecha Rishi S, Dalla-Pozza Luciano, Chenevix-Trench Georgia, Trahair Toby N, MacGregor Stuart, Schmiegelow Kje |
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Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.
Nature communications 2020 May 11 (1): 2254. Pirruccello James P, Bick Alexander, Wang Minxian, Chaffin Mark, Friedman Samuel, Yao Jie, Guo Xiuqing, Venkatesh Bharath Ambale, Taylor Kent D, Post Wendy S, Rich Stephen, Lima Joao A C, Rotter Jerome I, Philippakis Anthony, Lubitz Steven A, Ellinor Patrick T, Khera Amit V, Kathiresan Sekar, Aragam Krishna |
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Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection.
JAMA cardiology 2020 May . Turley Tamiel N, O'Byrne Megan M, Kosel Matthew L, de Andrade Mariza, Gulati Rajiv, Hayes Sharonne N, Tweet Marysia S, Olson Timothy |
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Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway.
Communications biology 2020 Apr 3 (1): 177. Manry Jeremy, Vincent Quentin B, Johnson Christian, Chrabieh Maya, Lorenzo Lazaro, Theodorou Ioannis, Ardant Marie-Françoise, Marion Estelle, Chauty Annick, Marsollier Laurent, Abel Laurent, Alcaïs Alexand |
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A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
Human genetics 2020 Apr . Justice Cristina M, Cuellar Araceli, Bala Krithi, Sabourin Jeremy A, Cunningham Michael L, Crawford Karen, Phipps Julie M, Zhou Yan, Cilliers Deirdre, Byren Jo C, Johnson David, Wall Steven A, Morton Jenny E V, Noons Peter, Sweeney Elizabeth, Weber Astrid, Rees Katie E M, Wilson Louise C, Simeonov Emil, Kaneva Radka, Yaneva Nadezhda, Georgiev Kiril, Bussarsky Assen, Senders Craig, Zwienenberg Marike, Boggan James, Roscioli Tony, Tamburrini Gianpiero, Barba Marta, Conway Kristin, Sheffield Val C, Brody Lawrence, Mills James L, Kay Denise, Sicko Robert J, Langlois Peter H, Tittle Rachel K, Botto Lorenzo D, Jenkins Mary M, LaSalle Janine M, Lattanzi Wanda, Wilkie Andrew O M, Wilson Alexander F, Romitti Paul A, Boyadjiev Simeon A, |
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Genetic Study of Severe Prolonged Lymphopenia in Multiple Sclerosis Patients Treated With Dimethyl Fumarate.
Frontiers in genetics 2019 10 1039. Sangurdekar Dipen, Sun Chao, McLaughlin Helen, Ayling-Rouse Katherine, Allaire Normand E, Penny Michelle A, Bronson Paola |
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Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.
American journal of human genetics 2020 Feb 106 (2): 264-271. Savage Sharon A, Viard Mathias, O'hUigin Colm, Zhou Weiyin, Yeager Meredith, Li Shengchao Alfred, Wang Tao, Ramsuran Veron, Vince Nicolas, Vogt Aurelie, Hicks Belynda, Burdett Laurie, Chung Charles, Dean Michael, de Andrade Kelvin C, Freedman Neal D, Berndt Sonja I, Rothman Nathaniel, Lan Qing, Cerhan James R, Slager Susan L, Zhang Yawei, Teras Lauren R, Haagenson Michael, Chanock Stephen J, Spellman Stephen R, Wang Youjin, Willis Amanda, Askar Medhat, Lee Stephanie J, Carrington Mary, Gadalla Shahinaz |
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Genetic Association and Expression Correlation between Colony-Stimulating Factor 1 Gene Encoding M-CSF and Adult-Onset Still's Disease.
Journal of immunology research 2020 2020 8640719. Chen Yi-Ming, Hung Wei-Ting, Chang Wan-Chun, Hsieh Chia-Wei, Chung Wen-Hung, Lan Joung-Liang, Gung Ning-Rong, Lee Yun-Shien, Chen Der-Yuan, Hung Shuen- |
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Identification of a new genetic variant associated with cholecystitis: a multicenter genome-wide association study.
The journal of trauma and acute care surgery 2020 Feb . Bonde Alexander, Gaitanidis Apostolos, Breen Kerry, El Hechi Majed, Nederpelt Charlie, Christensen Mathias, Kokoroskos Nikolaos, Mendoza April, Velmahos George, Sillesen Martin, Farhat Maha R, Kaafarani Haytham M |
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Genetic associations with clozapine-induced myocarditis in patients with schizophrenia.
Translational psychiatry 2020 Jan 10 (1): 37. Lacaze Paul, Ronaldson Kathlyn J, Zhang Eunice J, Alfirevic Ana, Shah Hardik, Newman Leah, Strahl Maya, Smith Melissa, Bousman Chad, Francis Ben, Morris Andrew P, Wilson Trevor, Rossello Fernando, Powell David, Vasic Vivien, Sebra Robert, McNeil John J, Pirmohamed Mun |
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Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis.
Rheumatology international 2020 Feb . Condreay Lynn D, Parham Laura R, Qu Xiaoyan A, Steinfeld Jonathan, Wechsler Michael E, Raby Benjamin A, Yancey Steven W, Ghosh Soumit |
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Genome-Wide Association Study of Cryptosporidiosis in Infants Implicates
mBio 2020 Feb 11 (1): . Wojcik Genevieve L, Korpe Poonum, Marie Chelsea, Mentzer Alexander J, Carstensen Tommy, Mychaleckyj Josyf, Kirkpatrick Beth D, Rich Stephen S, Concannon Patrick, Faruque A S G, Haque Rashidul, Petri William A, Duggal Pri |
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Sepsis-associated acute respiratory distress syndrome in individuals of European ancestry: a genome-wide association study.
The Lancet. Respiratory medicine 2020 Jan . Guillen-Guio Beatriz, Lorenzo-Salazar Jose M, Ma Shwu-Fan, Hou Pei-Chi, Hernandez-Beeftink Tamara, Corrales Almudena, García-Laorden M Isabel, Jou Jonathan, Espinosa Elena, Muriel Arturo, Domínguez David, Lorente Leonardo, Martín María M, Rodríguez-Gallego Carlos, Solé-Violán Jordi, Ambrós Alfonso, Carriedo Demetrio, Blanco Jesús, Añón José M, Reilly John P, Jones Tiffanie K, Ittner Caroline Ag, Feng Rui, Schöneweck Franziska, Kiehntopf Michael, Noth Imre, Scholz Markus, Brunkhorst Frank M, Scherag André, Meyer Nuala J, Villar Jesús, Flores Carl |
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Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status.
Nature communications 2019 Nov 10 (1): 5120. Lyons Paul A, Peters James E, Alberici Federico, Liley James, Coulson Richard M R, Astle William, Baldini Chiara, Bonatti Francesco, Cid Maria C, Elding Heather, Emmi Giacomo, Epplen Jörg, Guillevin Loïc, Jayne David R W, Jiang Tao, Gunnarsson Iva, Lamprecht Peter, Leslie Stephen, Little Mark A, Martorana Davide, Moosig Frank, Neumann Thomas, Ohlsson Sophie, Quickert Stefanie, Ramirez Giuseppe A, Rewerska Barbara, Schett Georg, Sinico Renato A, Szczeklik Wojciech, Tesar Vladimir, Vukcevic Damjan, , Terrier Benjamin, Watts Richard A, Vaglio Augusto, Holle Julia U, Wallace Chris, Smith Kenneth G |
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A meta-analysis of genome-wide association studies of multiple myeloma among men and women of African ancestry.
Blood advances 2020 Jan 4 (1): 181-190. Du Zhaohui, Weinhold Niels, Song Gregory Chi, Rand Kristin A, Van Den Berg David J, Hwang Amie E, Sheng Xin, Hom Victor, Ailawadhi Sikander, Nooka Ajay K, Singhal Seema, Pawlish Karen, Peters Edward S, Bock Cathryn, Mohrbacher Ann, Stram Alexander, Berndt Sonja I, Blot William J, Casey Graham, Stevens Victoria L, Kittles Rick, Goodman Phyllis J, Diver W Ryan, Hennis Anselm, Nemesure Barbara, Klein Eric A, Rybicki Benjamin A, Stanford Janet L, Witte John S, Signorello Lisa, John Esther M, Bernstein Leslie, Stroup Antoinette M, Stephens Owen W, Zangari Maurizio, Van Rhee Frits, Olshan Andrew, Zheng Wei, Hu Jennifer J, Ziegler Regina, Nyante Sarah J, Ingles Sue Ann, Press Michael F, Carpten John David, Chanock Stephen J, Mehta Jayesh, Colditz Graham A, Wolf Jeffrey, Martin Thomas G, Tomasson Michael, Fiala Mark A, Terebelo Howard, Janakiraman Nalini, Kolonel Laurence, Anderson Kenneth C, Le Marchand Loic, Auclair Daniel, Chiu Brian C-H, Ziv Elad, Stram Daniel, Vij Ravi, Bernal-Mizrachi Leon, Morgan Gareth J, Zonder Jeffrey A, Huff Carol Ann, Lonial Sagar, Orlowski Robert Z, Conti David V, Haiman Christopher A, Cozen Wen |
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Identification of
Neurology. Genetics 2019 Dec 5 (6): e375. Wei Ling, Tian Yanghua, Chen Yongping, Wei Qianqian, Chen Fangfang, Cao Bei, Wu Ying, Zhao Bi, Chen Xueping, Xie Chengjuan, Xi Chunhua, Yu Xu'en, Wang Juan, Lv Xinyi, Du Jing, Wang Yu, Shen Lu, Wang Xin, Shen Bin, Guo Qihao, Guo Li, Xia Kun, Xie Peng, Zhang Xuejun, Zuo Xianbo, Shang Huifang, Wang K |
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Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy.
Communications biology 2019 2 468. Hosoda Yoshikatsu, Miyake Masahiro, Schellevis Rosa L, Boon Camiel J F, Hoyng Carel B, Miki Akiko, Meguro Akira, Sakurada Yoichi, Yoneyama Seigo, Takasago Yukari, Hata Masayuki, Muraoka Yuki, Nakanishi Hideo, Oishi Akio, Ooto Sotaro, Tamura Hiroshi, Uji Akihito, Miyata Manabu, Takahashi Ayako, Ueda-Arakawa Naoko, Tajima Atsushi, Sato Takehiro, Mizuki Nobuhisa, Shiragami Chieko, Iida Tomohiro, Khor Chiea Chuen, Wong Tien Yin, Yamada Ryo, Honda Shigeru, de Jong Eiko K, Hollander Anneke I den, Matsuda Fumihiko, Yamashiro Kenji, Tsujikawa Akita |
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Association of Genetic Variation With Keratoconus.
JAMA ophthalmology 2019 Dec . McComish Bennet J, Sahebjada Srujana, Bykhovskaya Yelena, Willoughby Colin E, Richardson Andrea J, Tenen Abi, Charlesworth Jac C, MacGregor Stuart, Mitchell Paul, Lucas Sionne E M, Mills Richard A, Mackey David A, Li Xiaohui, Wang Jie Jin, Jensen Richard A, Rotter Jerome I, Taylor Kent D, Hewitt Alex W, Rabinowitz Yaron S, Baird Paul N, Craig Jamie E, Burdon Kathryn |
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Non-del(5q) myelodysplastic syndromes-associated loci detected by SNP-array genome-wide association meta-analysis.
Blood advances 2019 Nov 3 (22): 3579-3589. McGraw Kathy L, Cheng Chia-Ho, Chen Y Ann, Hou Hsin-An, Nilsson Björn, Genovese Giulio, Cluzeau Thomas, Pellagatti Andrea, Przychodzen Bartlomiej P, Mallo Mar, Arenillas Leonor, Mohamedali Azim, Adès Lionel, Sallman David A, Padron Eric, Sokol Lubomir, Moreilhon Chimene, Raynaud Sophie, Tien Hwei-Fang, Boultwood Jacqueline, Ebert Benjamin L, Sole Francesc, Fenaux Pierre, Mufti Ghulam J, Maciejewski Jaroslaw P, Kanetsky Peter A, List Alan |
- Page last reviewed:Oct 1, 2020
- Page last updated:Dec 23, 2020
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