Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 75 Records) |
| Query Trace: Disease and SH2B3[original query] |
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| The SH2B3 and KCNK5 loci may be implicated in regulation of platelet count, volume, and maturity. Thrombosis research 2017 Aug 158 86-92. Christiansen Morten K, Larsen Sanne B, Nyegaard Mette, Neergaard-Petersen Søs, Würtz Morten, Grove Erik L, Hvas Anne-Mette, Jensen Henrik K, Kristensen Steen |
| Sex-specific association of SH2B3 and SMARCA4 polymorphisms with coronary artery disease susceptibility. Oncotarget 2017 Aug 8 (35): 59397-59407. Ji Yuqiang, Song Yanbin, Wang Qingwen, Xu Pengcheng, Zhao Zhao, Li Xia, Wang Nan, Jin Tianbo, Chen Ch |
| Association of autoimmune hepatitis with Src homology 2 adaptor protein 3 gene polymorphisms in Japanese patients. Journal of human genetics 2017 Nov 62 (11): 963-967. Umemura Takeji, Joshita Satoru, Hamano Hideaki, Yoshizawa Kaname, Kawa Shigeyuki, Tanaka Eiji, Ota Mas |
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.
Nature communications 2017 Oct 8 (1): 910. Joshi Peter K, Pirastu Nicola, Kentistou Katherine A, Fischer Krista, Hofer Edith, Schraut Katharina E, Clark David W, Nutile Teresa, Barnes Catriona L K, Timmers Paul R H J, Shen Xia, Gandin Ilaria, McDaid Aaron F, Hansen Thomas Folkmann, Gordon Scott D, Giulianini Franco, Boutin Thibaud S, Abdellaoui Abdel, Zhao Wei, Medina-Gomez Carolina, Bartz Traci M, Trompet Stella, Lange Leslie A, Raffield Laura, van der Spek Ashley, Galesloot Tessel E, Proitsi Petroula, Yanek Lisa R, Bielak Lawrence F, Payton Antony, Murgia Federico, Concas Maria Pina, Biino Ginevra, Tajuddin Salman M, Seppälä Ilkka, Amin Najaf, Boerwinkle Eric, Børglum Anders D, Campbell Archie, Demerath Ellen W, Demuth Ilja, Faul Jessica D, Ford Ian, Gialluisi Alessandro, Gögele Martin, Graff MariaElisa, Hingorani Aroon, Hottenga Jouke-Jan, Hougaard David M, Hurme Mikko A, Ikram M Arfan, Jylhä Marja, Kuh Diana, Ligthart Lannie, Lill Christina M, Lindenberger Ulman, Lumley Thomas, Mägi Reedik, Marques-Vidal Pedro, Medland Sarah E, Milani Lili, Nagy Reka, Ollier William E R, Peyser Patricia A, Pramstaller Peter P, Ridker Paul M, Rivadeneira Fernando, Ruggiero Daniela, Saba Yasaman, Schmidt Reinhold, Schmidt Helena, Slagboom P Eline, Smith Blair H, Smith Jennifer A, Sotoodehnia Nona, Steinhagen-Thiessen Elisabeth, van Rooij Frank J A, Verbeek André L, Vermeulen Sita H, Vollenweider Peter, Wang Yunpeng, Werge Thomas, Whitfield John B, Zonderman Alan B, Lehtimäki Terho, Evans Michele K, Pirastu Mario, Fuchsberger Christian, Bertram Lars, Pendleton Neil, Kardia Sharon L R, Ciullo Marina, Becker Diane M, Wong Andrew, Psaty Bruce M, van Duijn Cornelia M, Wilson James G, Jukema J Wouter, Kiemeney Lambertus, Uitterlinden André G, Franceschini Nora, North Kari E, Weir David R, Metspalu Andres, Boomsma Dorret I, Hayward Caroline, Chasman Daniel, Martin Nicholas G, Sattar Naveed, Campbell Harry, Esko T?nu, Kutalik Zoltán, Wilson James |
| Co-occurrence of Type 1 Diabetes and Celiac Disease Autoimmunity. Pediatrics 2017 Oct . Hagopian William, Lee Hye-Seung, Liu Edwin, Rewers Marian, She Jin-Xiong, Ziegler Anette-G, Lernmark Åke, Toppari Jorma, Rich Stephen S, Krischer Jeffrey P, Erlich Henry, Akolkar Beena, Agardh Daniel, |
| Role of SH2B3 R262W gene polymorphism and risk of coronary heart disease: A PRISMA-compliant meta-analysis. Medicine 2018 Nov 97 (48): e13436. Hong Lu, Jiang Yu-Feng, Chen Min, Zhang Nan-Nan, Yang Hua-Jia, Rui Qing, Zhou Ya-Fe |
| Association of STAT4, TGF?1, SH2B3 and PTPN22 polymorphisms with autoimmune hepatitis. Experimental and molecular pathology 2018 Oct 105 (3): 279-284. Chaouali Marwa, Fernandes Veronica, Ghazouani Ezzedine, Pereira Luisa, Kochkar Radh |
| Allogeneic stem cell transplantation in patients with myelofibrosis harboring the MPL mutation. European journal of haematology 2019 Aug . Mannina Daniele, Gagelmann Nico, Badbaran Anita, Ditschkowski Markus, Bogdanov Rashit, Robin Marie, Cassinat Bruno, Heuser Michael, Shahswar Rabia, Thol Felicitas, Beelen Dietrich, Kröger Nicola |
| The Longevity-Associated SH2B3 (LNK) Genetic Variant: Selected Aging Phenotypes in 379,758 Subjects. The journals of gerontology. Series A, Biological sciences and medical sciences 2019 8 75 (9): 1656-1662. Kuo Chia-Ling, Joaquim Micaella, Kuchel George A, Ferrucci Luigi, Harries Lorna W, Pilling Luke C, Melzer Dav |
| Targeted Sequencing Study to Uncover Shared Genetic Susceptibility Between Peripheral Artery Disease and Coronary Heart Disease-Brief Report. Arteriosclerosis, thrombosis, and vascular biology 2019 Apr ATVBAHA118312128. Safarova Maya S, Fan Xiao, Austin Erin E, van Zuydam Natalie, Hopewell Jemma, Schaid Daniel J, Kullo Iftikhar |
| Integrative Genomic Analysis Reveals Cancer-Associated Gene Mutations in Chronic Myeloid Leukemia Patients with Resistance or Intolerance to Tyrosine Kinase Inhibitor. OncoTargets and therapy 2020 9 13 8581-8591. Wu Waner, Xu Na, Zhou Xuan, Liu Liang, Tan Yaxian, Luo Jie, Huang Jixian, Qin Jiayue, Wang Juan, Li Zhimin, Yin Changxin, Zhou Lingling, Liu Xiao |
| Influence of SH2B3, MTHFD1L, GGCX, and ITGB3 Gene Polymorphisms on theVariability on Warfarin Dosage Requirements and Susceptibility to CVD in the Jordanian Population. Journal of personalized medicine 2020 9 10 (3): . Al-Eitan Laith N, Almasri Ayah Y, Khasawneh Rame H, Alghamdi Mansour |
| Type 1 Diabetes and Autoimmune Thyroid Disease-The Genetic Link. Frontiers in endocrinology 2021 3 12 618213. Frommer Lara, Kahaly George |
| Pediatric Non-Alcoholic Fatty Liver Disease is Affected by Genetic Variants Involved in Lifespan/Healthspan. Journal of pediatric gastroenterology and nutrition 2021 Mar . Crudele Annalisa, Dato Serena, Re Oriana Lo, Maugeri Andrea, Sanna Paola, Giallongo Sebastiano, Oben Jude, Panera Nadia, De Rango Francesco, Mosca Antonella, Rose Giuseppina, Passarino Giuseppe, Alisi Anna, Vinciguerra Manl |
| Clonal Hematopoiesis-Associated Gene Mutations in a Clinical Cohort of 448 Patients With Ovarian Cancer. Journal of the National Cancer Institute 2021 12 114 (4): 565-570. Weber-Lassalle Konstantin, Ernst Corinna, Reuss Alexander, Möllenhoff Kathrin, Baumann Klaus, Jackisch Christian, Hauke Jan, Dietrich Dimo, Borde Julika, Park-Simon Tjoung-Won, Hanker Lars, Prieske Katharina, Schmidt Sandra, Weber-Lassalle Nana, Pohl-Rescigno Esther, Kommoss Stefan, Marmé Frederik, Heitz Florian, Stingl Julia C, Schmutzler Rita K, Harter Philipp, Hahnen Er |
| Integrated Clinical Genotype-Phenotype Characteristics of Blastic Plasmacytoid Dendritic Cell Neoplasm. Cancers 2021 12 13 (23): . Yin C Cameron, Pemmaraju Naveen, You M James, Li Shaoying, Xu Jie, Wang Wei, Tang Zhenya, Alswailmi Omar, Bhalla Kapil N, Qazilbash Muzaffar H, Konopleva Marina, Khoury Joseph |
| Genome-Wide Association Study of Peripheral Artery Disease.
Circulation. Genomic and precision medicine 2021 Oct CIRCGEN119002862. van Zuydam Natalie R, Stiby Alexander, Abdalla Moustafa, Austin Erin, Dahlström Emma H, McLachlan Stela, Vlachopoulou Efthymia, Ahlqvist Emma, Di Liao Chen, Sandholm Niina, Forsblom Carol, Mahajan Anubha, Robertson Neil R, Rayner N William, Lindholm Eero, Sinisalo Juha, Perola Markus, Kallio Milla, Weiss Emily, Price Jackie, Paterson Andrew, Klein Barbara, Salomaa Veikko, Palmer Colin N A, Groop Per-Henrik, Groop Leif, McCarthy Mark I, de Andrade Mariza, Morris Andrew P, Hopewell Jemma C, Colhoun Helen M, Kullo Iftikhar J, |
| Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes. Journal of human genetics 2021 Jan . Cerqueira Juliana X M, Saavalainen Päivi, Kurppa Kalle, Laurikka Pilvi, Huhtala Heini, Nykter Matti, L E Koskinen Lotta, Yohannes Dawit A, Kilpeläinen Elina, Shcherban Anastasia, Palotie Aarno, Kaukinen Katri, Lindfors Kat |
| The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene. Scientific reports 2021 Aug 11 (1): 15652. Bagheri Minoo, Wang Chuan, Shi Mingjian, Manouchehri Ali, Murray Katherine T, Murphy Matthew B, Shaffer Christian M, Singh Kritika, Davis Lea K, Jarvik Gail P, Stanaway Ian B, Hebbring Scott, Reilly Muredach P, Gerszten Robert E, Wang Thomas J, Mosley Jonathan D, Ferguson Jane |
| Exploring potential shared genetic influences between rheumatoid arthritis and blood lipid levels. Atherosclerosis 2022 12 363 48-56. Kasher Melody, Cherny Stacey S, , Livshits Grego |
| Coronary artery disease risk factors affected by RNA modification-related genetic variants. Frontiers in cardiovascular medicine 2022 9 985121. Li Ru, Zhang Huan, Tang Fan, Duan Chengcheng, Liu Dan, Wu Naqiong, Zhang Yonghong, Wang Laiyuan, Mo Xing |
| Biallelic deleterious germline SH2B3 variants cause a novel syndrome of myeloproliferation and multi-organ autoimmunity. EJHaem 2023 5 4 (2): 463-469. Piers Blombery, Vahid Pazhakh, Adriana S Albuquerque, Jesmeen Maimaris, Lingge Tu, Brenda Briones Miranda, Florence Evans, Ella R Thompson, Ben Carpenter, Ian Proctor, Julie A Curtin, Jonathan Lambert, Siobhan O Burns, Graham J Liesch |
| DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
| Polycystic Ovarian Syndrome Physiologic Pathways Implicated Through Clustering of Genetic Loci. The Journal of clinical endocrinology and metabolism 2023 11 . Maria I Stamou, Kirk T Smith, Hyunkyung Kim, Ravikumar Balasubramanian, Kathryn J Gray, Miriam Udl |
| CTLA4, SH2B3 and CLEC16A diversely affect the progression of early islet autoimmunity in relatives of type 1 diabetes patients. Clinical and experimental immunology 2023 1 . Vandewalle Julie, Desouter Aster K, Van der Auwera Bart J, Tenoutasse Sylvie, Gillard Pieter, De Block Christophe, Keymeulen Bart, Gorus Frans K, Van de Casteele Mark, |
| Replication of association at the LPP and UBASH3A loci in a UK autoimmune Addison's disease cohort. European journal of endocrinology 2023 1 188 (1): . Howarth Sophie, Sneddon Georgina, Allinson Kathleen R, Razvi Salman, Mitchell Anna L, Pearce Simon H |
| Src homology 2-B adapter protein 3 C784 T and Methylenetetrahydrofolate reductase C677 T Polymorphisms and Inflammation Markers in ST-segment Elevation Myocardial Infarction Patients. Angiology 2023 1 33197231152693. Golestani Amin, Rahimi Atefeh, Moezi Bady Seyed Ali, Azdaki Nahid, Sajjadi Seyed Meh |
| Six genetic variants are associated with cardiovascular disease independently from canonical risk factors: a new method to refine GWAS results based on the UKBiobank phenotype database. Molecular genetics and genomics : MGG 2024 12 300 (1): 4. Davide Noto, Carola Maria Gagliardo, Rossella Spina, Antonina Giammanco, Marcello Ciaccio, Angelo B Cefalù, Maurizio Aver |
| Fine-mapping and molecular characterisation of primary sclerosing cholangitis genetic risk loci. Nature communications 2024 11 15 (1): 9594. Elizabeth C Goode, Laura Fachal, Nikolaos Panousis, Loukas Moutsianas, Rebecca E McIntyre, Benjamin Yu Hang Bai, Norihito Kawasaki, Alexandra Wittmann, Tim Raine, Simon M Rushbrook, Carl A Anders |
| Mapping inherited genetic variation with opposite effects on autoimmune disease and cancer identifies candidate drug targets associated with the anti-tumor immune response. medRxiv : the preprint server for health sciences 2024 1 . Junyu Chen, Michael P Epstein, Joellen M Schildkraut, Siddhartha P K |
- Page last reviewed:Feb 1, 2024
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