Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: BSN[original query] |
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Effect of BSN-MST1 locus on inflammatory bowel disease and multiple sclerosis susceptibility. Genes and immunity 2009 Oct 10 (7): 631-5. Márquez A, Cénit M C, Núñez C, Mendoza J L, Taxonera C, Díaz-Rubio M, Bartolomé M, Arroyo R, Fernández-Arquero M, de la Concha E G, Urcelay |
Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. The British journal of psychiatry : the journal of mental science 2009 Jul 195 (1): 23-9. Hamshere M L, Green E K, Jones I R, Jones L, Moskvina V, Kirov G, Grozeva D, Nikolov I, Vukcevic D, Caesar S, Gordon-Smith K, Fraser C, Russell E, Breen G, St Clair D, Collier D A, Young A H, Ferrier I N, Farmer A, McGuffin P, , Holmans P A, Owen M J, O'Donovan M C, Craddock |
Variants at the 3p21 locus influence susceptibility and phenotype both in adults and early-onset patients with inflammatory bowel disease. Inflammatory bowel diseases 2010 Jul 16 (7): 1108-17. Latiano Anna, Palmieri Orazio, Corritore Giuseppe, Valvano Maria Rosa, Bossa Fabrizio, Cucchiara Salvatore, Castro Massimo, Riegler Gabriele, De Venuto Domenica, D'Incà Renata, Andriulli Angelo, Annese Vi |
Target sequencing of 307 deafness genes identifies candidate genes implicated in microtia. Oncotarget 2017 Sep 8 (38): 63324-63332. Wang Pu, Fan Xinmiao, Wang Yibei, Fan Yue, Liu Yaping, Zhang Shuyang, Chen Xiaow |
The mutational landscape and prognostic indicators of pseudomyxoma peritonei originating from the ovary. International journal of cancer 2021 1 148 (8): 2036-2047. Wang Bing, Yao Jianfei, Ma Ruiqing, Liu Danni, Lu Yiyan, Shi Guanjun, An Lubiao, Xia Ao, Chen Feng, Pang Shaojun, Zhai Xichao, Liu Guifeng, Chen Shifu, Xu Mingyan, Song Lele, Xu Hongb |
Genetics of progressive supranuclear palsy in a Chinese population. Neurobiology of disease 2022 Jul 172 105819. Xiao Xuewen, Yang Qijie, Wen Yafei, Jiao Bin, Liao Xinxin, Zhou Yafang, Weng Ling, Liu Hui, Xu Tianyan, Zhu Yuan, Guo Lina, Zhou Lu, Wang Xin, Liu Xixi, Bi Xiangyun, Liu Yingzi, Zhang Sizhe, Zhang Weiwei, Li Jinchen, Tang Beisha, Shen |
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes.
Brain : a journal of neurology 2022 1 145 (2): 555-568. Skotte Line, Fadista João, Bybjerg-Grauholm Jonas, Appadurai Vivek, Hildebrand Michael S, Hansen Thomas F, Banasik Karina, Grove Jakob, Albiñana Clara, Geller Frank, Bjurström Carmen F, Vilhjálmsson Bjarni J, Coleman Matthew, Damiano John A, Burgess Rosemary, Scheffer Ingrid E, Pedersen Ole Birger Vesterager, Erikstrup Christian, Westergaard David, Nielsen Kaspar René, Sørensen Erik, Bruun Mie Topholm, Liu Xueping, Hjalgrim Henrik, Pers Tune H, Mortensen Preben Bo, Mors Ole, Nordentoft Merete, Dreier Julie W, Børglum Anders D, Christensen Jakob, Hougaard David M, Buil Alfonso, Hviid Anders, Melbye Mads, Ullum Henrik, Berkovic Samuel F, Werge Thomas, Feenstra Bjar |
Association between Taxonomic Composition of Gut Microbiota and Host Single Nucleotide Polymorphisms in Crohn's Disease Patients from Russia. International journal of molecular sciences 2023 5 24 (9): . Maria Markelova, Anastasia Senina, Dilyara Khusnutdinova, Maria Siniagina, Elena Kupriyanova, Gulnaz Shakirova, Alfiya Odintsova, Rustam Abdulkhakov, Irina Kolesnikova, Olga Shagaleeva, Svetlana Lyamina, Sayar Abdulkhakov, Natalia Zakharzhevskaya, Tatiana Grigorye |
Predicted loss of function alleles in Bassoon (BSN) are associated with obesity. medRxiv : the preprint server for health sciences 2023 3 . Zhu Na, LeDuc Charles A, Fennoy Ilene, Laferr Re Blandine, Doege Claudia A, Shen Yufeng, Chung Wendy K, Leibel Rudolph |
The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson's Disease in India. Movement disorders : official journal of the Movement Disorder Society 2023 11 . Shan V Andrews, Prashanth L Kukkle, Ramesh Menon, Thenral S Geetha, Vinay Goyal, Rukmini Mridula Kandadai, Hrishikesh Kumar, Rupam Borgohain, Adreesh Mukherjee, Pettarusp M Wadia, Ravi Yadav, Soaham Desai, Niraj Kumar, Deepika Joshi, Sakthivel Murugan, Atanu Biswas, Pramod K Pal, Merina Oliver, Sandhya Nair, Anbu Kayalvizhi, Praveena L Samson, Manjari Deshmukh, Akshi Bassi, Charugulla Sandeep, Nitin Mandloi, Oliver B Davis, Melissa A Roberts, Dara E Leto, Anastasia G Henry, Gilbert Di Paolo, Uday Muthane, Shymal K Das, Andrew S Peterson, Thomas Sandmann, Ravi Gupta, Vedam L Ramprasad, |
Rare predicted loss of function alleles in Bassoon (BSN) are associated with obesity. NPJ genomic medicine 2023 10 8 (1): 33. Na Zhu, Charles A LeDuc, Ilene Fennoy, Blandine Laferrère, Claudia A Doege, Yufeng Shen, Wendy K Chung, Rudolph L Leib |
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Nature genetics 2023 3 55 (3): 423-436. Rahmioglu Nilufer, Mortlock Sally, Ghiasi Marzieh, Møller Peter L, Stefansdottir Lilja, Galarneau Geneviève, Turman Constance, Danning Rebecca, Law Matthew H, Sapkota Yadav, Christofidou Paraskevi, Skarp Sini, Giri Ayush, Banasik Karina, Krassowski Michal, Lepamets Maarja, Marciniak B?a?ej, Nõukas Margit, Perro Danielle, Sliz Eeva, Sobalska-Kwapis Marta, Thorleifsson Gudmar, Topbas-Selcuki Nura F, Vitonis Allison, Westergaard David, Arnadottir Ragnheidur, Burgdorf Kristoffer S, Campbell Archie, Cheuk Cecilia S K, Clementi Caterina, Cook James, De Vivo Immaculata, DiVasta Amy, Dorien O, Donoghue Jacqueline F, Edwards Todd, Fontanillas Pierre, Fung Jenny N, Geirsson Reynir T, Girling Jane E, Harkki Paivi, Harris Holly R, Healey Martin, Heikinheimo Oskari, Holdsworth-Carson Sarah, Hostettler Isabel C, Houlden Henry, Houshdaran Sahar, Irwin Juan C, Jarvelin Marjo-Riitta, Kamatani Yoichiro, Kennedy Stephen H, Kepka Ewa, Kettunen Johannes, Kubo Michiaki, Kulig Bartosz, Kurra Venla, Laivuori Hannele, Laufer Marc R, Lindgren Cecilia M, MacGregor Stuart, Mangino Massimo, Martin Nicholas G, Matalliotaki Charoula, Matalliotakis Michail, Murray Alison D, Ndungu Anne, Nezhat Camran, Olsen Catherine M, Opoku-Anane Jessica, Padmanabhan Sandosh, Paranjpe Manish, Peters Maire, Polak Grzegorz, Porteous David J, Rabban Joseph, Rexrode Kathyrn M, Romanowicz Hanna, Saare Merli, Saavalainen Liisu, Schork Andrew J, Sen Sushmita, Shafrir Amy L, Siewierska-Górska Anna, S?omka Marcin, Smith Blair H, Smolarz Beata, Szaflik Tomasz, Szy??o Krzysztof, Takahashi Atsushi, Terry Kathryn L, Tomassetti Carla, Treloar Susan A, Vanhie Arne, Vincent Katy, Vo Kim C, Werring David J, Zeggini Eleftheria, Zervou Maria I, , , , , , Adachi Sosuke, Buring Julie E, Ridker Paul M, D'Hooghe Thomas, Goulielmos George N, Hapangama Dharani K, Hayward Caroline, Horne Andrew W, Low Siew-Kee, Martikainen Hannu, Chasman Daniel I, Rogers Peter A W, Saunders Philippa T, Sirota Marina, Spector Tim, Strapagiel Dominik, Tung Joyce Y, Whiteman David C, Giudice Linda C, Velez-Edwards Digna R, Uimari Outi, Kraft Peter, Salumets Andres, Nyholt Dale R, Mägi Reedik, Stefansson Kari, Becker Christian M, Yurttas-Beim Piraye, Steinthorsdottir Valgerdur, Nyegaard Mette, Missmer Stacey A, Montgomery Grant W, Morris Andrew P, Zondervan Krina |
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease. Nature genetics 2024 4 . Yajie Zhao, Maria Chukanova, Katherine A Kentistou, Zammy Fairhurst-Hunter, Anna Maria Siegert, Raina Y Jia, Georgina K C Dowsett, Eugene J Gardner, Katherine Lawler, Felix R Day, Lena R Kaisinger, Yi-Chun Loraine Tung, Brian Yee Hong Lam, Hsiao-Jou Cortina Chen, Quanli Wang, Jaime Berumen-Campos, Pablo Kuri-Morales, Roberto Tapia-Conyer, Jesus Alegre-Diaz, Inês Barroso, Jonathan Emberson, Jason M Torres, Rory Collins, Danish Saleheen, Katherine R Smith, Dirk S Paul, Florian Merkle, I Sadaf Farooqi, Nick J Wareham, Slavé Petrovski, Stephen O'Rahilly, Ken K Ong, Giles S H Yeo, John R B Per |
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