HuGE Literature Finder
Neurological Disorders
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Integration of Transcriptome and Exome Genotyping Identifies Significant Variants with Autism Spectrum Disorder.
![]() Pharmaceuticals (Basel, Switzerland) 2022 Jan 15 (2): . Almandil Noor B, AlSulaiman Abdulla, Aldakeel Sumayh A, Alkuroud Deem N, Aljofi Halah Egal, Alzahrani Safah, Al-Mana Aishah, Alfuraih Asma A, Alabdali Majed, Alkhamis Fahd A, AbdulAzeez Sayed, Borgio J Franc |
Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study.
![]() Proceedings of the National Academy of Sciences of the United States of America 2022 02 119 (5): . Chia Ruth, Saez-Atienzar Sara, Murphy Natalie, Chiò Adriano, Blauwendraat Cornelis, , Roda Ricardo H, Tienari Pentti J, Kaminski Henry J, Ricciardi Roberta, Guida Melania, De Rosa Anna, Petrucci Loredana, Evoli Amelia, Provenzano Carlo, Drachman Daniel B, Traynor Bryan |
GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion.
![]() Scientific reports 2022 01 12 (1): 1332. Kasai Mariko, Omae Yosuke, Kawai Yosuke, Shibata Akiko, Hoshino Ai, Mizuguchi Masashi, Tokunaga Katsus |
Use of Deep-Learning Genomics to Discriminate Healthy Individuals from Those with Alzheimer's Disease or Mild Cognitive Impairment.
![]() Behavioural neurology 2021 8 2021 3359103. Li Lanlan, Yang Yeying, Zhang Qi, Wang Jiao, Jiang Jiehui, Neuroimaging Initiative Alzheimer's Disea |
A two-stage genome-wide association study of radiation-induced acute toxicity in head and neck cancer.
![]() Journal of translational medicine 2021 11 19 (1): 481. Naderi Elnaz, Crijns Anne Petra Gerarda, Steenbakkers Roel Johannes Henricus Marinus, van den Hoek Johanna Geertruida Maria, Boezen Hendrika Marike, Alizadeh Behrooz Ziad, Langendijk Johannes Albert |
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus.
![]() Human molecular genetics 2021 Dec . Suetsugu Hiroyuki, Kim Kwangwoo, Yamamoto Takuaki, Bang So-Young, Sakamoto Yuma, Shin Jung-Min, Sugano Nobuhiko, Kim Ji Soong, Mukai Masaya, Lee Yeon-Kyung, Ohmura Koichiro, Park Dae Jin, Takahashi Daisuke, Ahn Ga-Young, Karino Kohei, Kwon Young-Chang, Miyamura Tomoya, Kim Jihye, Nakamura Junichi, Motomura Goro, Kuroda Takeshi, Niiro Hiroaki, Miyamoto Takeshi, Takeuchi Tsutomu, Ikari Katsunori, Amano Koichi, Tada Yoshifumi, Yamaji Ken, Shimizu Masato, Atsumi Takashi, Seki Taisuke, Tanaka Yoshiya, Kubo Toshikazu, Hisada Ryo, Yoshioka Tomokazu, Yamazaki Mihoko, Kabata Tamon, Kajino Tomomichi, Ohta Yoichi, Okawa Takahiro, Naito Yohei, Kaneuji Ayumi, Yasunaga Yuji, Ohzono Kenji, Tomizuka Kohei, Koido Masaru, Matsuda Koichi, Okada Yukinori, Suzuki Akari, Kim Bong-Jo, Kochi Yuta, Lee Hye-Soon, Ikegawa Shiro, Bae Sang-Cheol, Terao Chikas |
Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications.
![]() Frontiers in pharmacology 2021 6 12 688386. Wolking Stefan, Campbell Ciarán, Stapleton Caragh, McCormack Mark, Delanty Norman, Depondt Chantal, Johnson Michael R, Koeleman Bobby P C, Krause Roland, Kunz Wolfram S, Marson Anthony G, Sander Josemir W, Sills Graeme J, Striano Pasquale, Zara Federico, Sisodiya Sanjay M, Cavalleri Gianpiero L, Lerche Holg |
Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.
![]() American journal of human genetics 2021 7 108 (9): 1578-1589. Roychowdhury Tanmoy, Lu Haocheng, Hornsby Whitney E, Crone Bradley, Wang Gao T, Guo Dong-Chuan, Sendamarai Anoop K, Devineni Poornima, Lin Maoxuan, Zhou Wei, Graham Sarah E, Wolford Brooke N, Surakka Ida, Wang Zhenguo, Chang Lin, Zhang Jifeng, Mathis Michael, Brummett Chad M, Melendez Tori L, Shea Michael J, Kim Karen Meekyong, Deeb G Michael, Patel Himanshu J, Eliason Jonathan, Eagle Kim A, Yang Bo, Ganesh Santhi K, Brumpton Ben, Åsvold Bjørn Olav, Skogholt Anne Heidi, Hveem Kristian, , Pyarajan Saiju, Klarin Derek, Tsao Philip S, Damrauer Scott M, Leal Suzanne M, Milewicz Dianna M, Chen Y Eugene, Garcia-Barrio Minerva T, Willer Cristen |
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms.
![]() Nature communications 2021 7 12 (1): 4571. Ward Lucas D, Tu Ho-Chou, Quenneville Chelsea B, Tsour Shira, Flynn-Carroll Alexander O, Parker Margaret M, Deaton Aimee M, Haslett Patrick A J, Lotta Luca A, Verweij Niek, Ferreira Manuel A R, , , Baras Aris, Hinkle Gregory, Nioi Pa |
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
![]() European heart journal 2021 8 . Ahlberg Gustav, Andreasen Laura, Ghouse Jonas, Bertelsen Litten, Bundgaard Henning, Haunsø Stig, Svendsen Jesper H, Olesen Morten |
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction.
![]() Nature neuroscience 2021 8 24 (10): 1367-1376. Karlsson Linnér Richard, Mallard Travis T, Barr Peter B, Sanchez-Roige Sandra, Madole James W, Driver Morgan N, Poore Holly E, de Vlaming Ronald, Grotzinger Andrew D, Tielbeek Jorim J, Johnson Emma C, Liu Mengzhen, Rosenthal Sara Brin, Ideker Trey, Zhou Hang, Kember Rachel L, Pasman Joëlle A, Verweij Karin J H, Liu Dajiang J, Vrieze Scott, , Kranzler Henry R, Gelernter Joel, Harris Kathleen Mullan, Tucker-Drob Elliot M, Waldman Irwin D, Palmer Abraham A, Harden K Paige, Koellinger Philipp D, Dick Danielle |
Genome-Wide Meta-Analysis Identifies Two Novel Risk Loci for Epilepsy.
![]() Frontiers in neuroscience 2021 8 15 722592. Song Meng, Liu Jiewei, Yang Yongfeng, Lv Luxian, Li Wenqiang, Luo Xiong-Ji |
Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort.
![]() PloS one 2021 9 16 (9): e0247287. Ashvetiya Tamara, Fan Sherry X, Chen Yi-Ju, Williams Charles H, O'Connell Jeffery R, Perry James A, Hong Charles |
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions.
![]() Translational psychiatry 2021 9 11 (1): 451. Reus Lianne M, Jansen Iris E, Mol Merel O, van Ruissen Fred, van Rooij Jeroen, van Schoor Natasja M, Tesi Niccolò, Reinders Marcel J T, Huisman Martijn A, Holstege Henne, Visser Pieter Jelle, de Boer Sterre C M, Hulsman Marc, Ahmad Shahzad, Amin Najaf, Uitterlinden Andre G, Ikram Arfan, van Duijn Cornelia M, Seelaar Harro, Ramakers Inez H G B, Verhey Frans R J, van der Lugt Aad, Claassen Jurgen A H R, Jan Biessels Geert, De Deyn Peter Paul, Scheltens Philip, van der Flier Wiesje M, van Swieten John C, Pijnenburg Yolande A L, van der Lee Sven |
Pleiotropic predisposition to Alzheimer's disease and educational attainment: insights from the summary statistics analysis.
![]() GeroScience 2021 Nov . Kulminski Alexander M, Loiko Elena, Loika Yury, Culminskaya Iri |
Multi-ancestral GWAS identifies shared and Asian-specific loci for SLE and links type III interferon signaling and lysosomal function to the disease.
![]() Arthritis & rheumatology (Hoboken, N.J.) 2021 Nov . Wang Yong-Fei, Wei Wei, Tangtanatakul Pattarin, Zheng Lichuan, Lei Yao, Lin Zhiming, Qian Chengmin, Qin Xiao, Hou Fei, Zhang Xinyu, Shao Li, Satproedprai Nusara, Mahasirimongkol Surakameth, Pisitkun Prapaporn, Song Qin, Lau Yu Lung, Zhang Yan, Hirankarn Nattiya, Yang Wanli |
Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
![]() Journal of the American Heart Association 2021 Oct e022482. Leskelä Jaakko, Toppila Iiro, Härma Mari-Anne, Palviainen Teemu, Salminen Aino, Sandholm Niina, Pietiäinen Milla, Kopra Elisa, Pais de Barros Jean-Paul, , Lassenius Mariann I, Kumar Anmol, Harjutsalo Valma, Roslund Kajsa, Forsblom Carol, Loukola Anu, Havulinna Aki S, Lagrost Laurent, Salomaa Veikko, Groop Per-Henrik, Perola Markus, Kaprio Jaakko, Lehto Markku, Pussinen Pirkko |
Genome-wide association study of occupational attainment as a proxy for cognitive reserve.
![]() Brain : a journal of neurology 2021 Oct . Ko Hyunwoong, Kim Soyeon, Kim Kiwon, Jung Sang-Hyuk, Shim Injeong, Cha Soojin, Lee Hyewon, Kim Beomsu, Yoon Joohyun, Ha Tae Hyon, Kwak Seyul, Kang Jae Myeong, Lee Jun-Young, Kim Jinho, Park Woong-Yang, Nho Kwangsik, Kim Doh Kwan, Myung Woojae, Won Hong-H |
Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort.
![]() NeuroImage. Clinical 2021 Sep 32 102823. Zainul Abidin Fatin N, Scelsi Marzia A, Dawson Sally J, Altmann Andre, |
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.
![]() Nature genetics 2021 Sep 53 (9): 1276-1282. Wightman Douglas P, Jansen Iris E, Savage Jeanne E, Shadrin Alexey A, Bahrami Shahram, Holland Dominic, Rongve Arvid, Børte Sigrid, Winsvold Bendik S, Drange Ole Kristian, Martinsen Amy E, Skogholt Anne Heidi, Willer Cristen, Bråthen Geir, Bosnes Ingunn, Nielsen Jonas Bille, Fritsche Lars G, Thomas Laurent F, Pedersen Linda M, Gabrielsen Maiken E, Johnsen Marianne Bakke, Meisingset Tore Wergeland, Zhou Wei, Proitsi Petroula, Hodges Angela, Dobson Richard, Velayudhan Latha, , Sealock Julia M, Davis Lea K, Pedersen Nancy L, Reynolds Chandra A, Karlsson Ida K, Magnusson Sigurdur, Stefansson Hreinn, Thordardottir Steinunn, Jonsson Palmi V, Snaedal Jon, Zettergren Anna, Skoog Ingmar, Kern Silke, Waern Margda, Zetterberg Henrik, Blennow Kaj, Stordal Eystein, Hveem Kristian, Zwart John-Anker, Athanasiu Lavinia, Selnes Per, Saltvedt Ingvild, Sando Sigrid B, Ulstein Ingun, Djurovic Srdjan, Fladby Tormod, Aarsland Dag, Selbæk Geir, Ripke Stephan, Stefansson Kari, Andreassen Ole A, Posthuma Daniel |
Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population.
![]() Cephalalgia : an international journal of headache 2021 Aug 3331024211037269. Tsao Yu-Chien, Wang Shuu-Jiun, Hsu Chia-Lin, Wang Yen-Feng, Fuh Jong-Ling, Chen Shih-Pin, Fann Cathy Shen-Ja |
Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan.
![]() The journal of headache and pain 2021 Aug 22 (1): 89. Tsai Chia-Kuang, Liang Chih-Sung, Lin Guan-Yu, Tsai Chia-Lin, Lee Jiunn-Tay, Sung Yueh-Feng, Lin Yu-Kai, Hung Kuo-Sheng, Chen Wei-Liang, Yang Fu-C |
The BS variant of C4 protects against age-related loss of white matter microstructural integrity.
![]() Brain : a journal of neurology 2021 Aug . Traylor Matthew, Malik Rainer, Gesierich Benno, Dichgans Mart |
Genetic Variants Associated with Cytomegalovirus Infection after Allogeneic Hematopoietic Cell Transplantation.
![]() Blood 2021 Jul . Casto Amanda, Seo Sachiko, Levine David, Storer Barry E, Dong Xinyuan, Hansen John A, Boeckh Michael, Martin Paul |
Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci.
![]() Communications biology 2021 Jul 4 (1): 908. Qu Hui-Qi, Qu Jingchun, Bradfield Jonathan, Marchand Luc, Glessner Joseph, Chang Xiao, March Michael, Li Jin, Connolly John J, Roizen Jeffrey D, Sleiman Patrick, Polychronakos Constantin, Hakonarson Hak |
Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS).
![]() Clinical pharmacology and therapeutics 2021 Jul . McDonough Caitrin W, Warren Helen R, Jack John R, Motsinger-Reif Alison A, Armstrong Nicole D, Bis Joshua C, House John S, Singh Sonal, El Rouby Nihal M, Gong Yan, Mychaleckyj Joesyf C, Rotroff Daniel M, Benavente Oscar R, Caulfield Mark J, Doria Alessandrio, Pepine Carl J, Psaty Bruce M, Glorioso Valeria, Glorioso Nicola, Hiltunen Timo P, Kontula Kimmo K, Arnett Donna K, Buse John B, Irvin Marguerite R, Johnson Julie A, Munroe Patricia B, Wagner Michael J, Cooper-DeHoff Rhonda |
Characterizing the Genetic Architecture of Parkinson's Disease in Latinos.
![]() Annals of neurology 2021 Jul . Loesch Douglas P, Horimoto Andrea R V R, Heilbron Karl, Sarihan Elif Irem, Inca-Martinez Miguel, Mason Emily, Cornejo-Olivas Mario, Torres Luis, Mazzetti Pilar, Cosentino Carlos, Sarapura-Castro Elison, Rivera-Valdivia Andrea, Medina Angel C, Dieguez Elena, Raggio Victor, Lescano Andres, Tumas Vitor, Borges Vanderci, Ferraz Henrique B, Rieder Carlos R, Schumacher-Schuh Artur, Santos-Lobato Bruno L, Velez-Pardo Carlos, Jimenez-Del-Rio Marlene, Lopera Francisco, Moreno Sonia, Chana-Cuevas Pedro, Fernandez William, Arboleda Gonzalo, Arboleda Humberto, Arboleda-Bustos Carlos E, Yearout Dora, Zabetian Cyrus P, , Cannon Paul, Thornton Timothy A, O'Connor Timothy D, Mata Ignacio F, |
Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.
![]() Progress in neuro-psychopharmacology & biological psychiatry 2021 Jul 110393. Wang Kesheng, Xu Chun, Smith Amanda, Xiao Danqing, Navia R Osvaldo, Lu Yongke, Xie Changchun, Piamjariyakul Ubolrat, |
Genome Wide Association Study Identifies Risk Loci For Cluster Headache.
![]() Annals of neurology 2021 Jun . O'Connor Emer, Fourier Carmen, Ran Caroline, Sivakumar Prasanth, Liesecke Franziska, Southgate Laura, Harder Aster V E, Vijfhuizen Lisanne S, Yip Janice, Giffin Nicola, Silver Nicholas, Ahmed Fayyaz, Hostettler Isabel C, Davies Brendan, Cader M Zameel, Simpson Benjamin S, Sullivan Roisin, Efthymiou Stephanie, Adebimpe Joycee, Quinn Olivia, Campbell Ciaran, Cavalleri Gianpiero L, Vikelis Michail, Kelderman Tim, Paemeleire Koen, Kilbride Emer, Grangeon Lou, Lagrata Susie, Danno Daisuke, Trembath Richard, Wood Nicholas W, Kockum Ingrid, Winsvold Bendik S, Steinberg Anna, Sjöstrand Christina, Waldenlind Elisabet, Vandrovcova Jana, Houlden Henry, Matharu Manjit, Belin Andrea Carmi |
Genetic, Clinical, and Sociodemographic Factors Associated With Stimulant Treatment Outcomes in ADHD.
![]() The American journal of psychiatry 2021 Jun appiajp202020121686. Brikell Isabell, Wimberley Theresa, Albiñana Clara, Pedersen Emil Michael, Vilhjálmsson Bjarni Jóhann, Agerbo Esben, Demontis Ditte, Børglum Anders D, Schork Andrew J, LaBianca Sonja, Werge Thomas, Mors Ole, Hougaard David M, Thapar Anita, Mortensen Preben Bo, Dalsgaard Sør |
Identifying novel genetic variants for brain amyloid deposition: a genome-wide association study in the Korean population.
![]() Alzheimer's research & therapy 2021 06 13 (1): 117. Kim Hang-Rai, Jung Sang-Hyuk, Kim Jaeho, Jang Hyemin, Kang Sung Hoon, Hwangbo Song, Kim Jun Pyo, Kim So Yeon, Kim Beomsu, Kim Soyeon, Jeong Jee Hyang, Yoon Soo Jin, Park Kyung Won, Kim Eun-Joo, Yoon Bora, Jang Jae-Won, Hong Jin Yong, Choi Seong Hye, Noh Young, Kim Ko Woon, Kim Si Eun, Lee Jin San, Jung Na-Yeon, Lee Juyoun, Kim Byeong C, Son Sang Joon, Hong Chang Hyung, Na Duk L, Seo Sang Won, Won Hong-Hee, Kim Hee J |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jul 06, 2022
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