Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 96 Records) |
| Query Trace: Disease and HNF1A[original query] |
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| Association between CPR-related genetic variants and risk of ischemic stroke: a nested case-control study. Neurological research 2019 Oct 1-7. Zhu Yao, Hu Shu-Chang, Zheng Pei-Wen, Jin Ming-Juan, Tang Meng-Ling, Chen Kun, Wang Jian-Bi |
| High Prevalence of a Monogenic Cause in Han Chinese Diagnosed With Type 1 Diabetes, Partly Driven by Nonsyndromic Recessive WFS1 Mutations. Diabetes 2019 Oct . Li Meihang, Wang Sihua, Xu Kuanfeng, Chen Yang, Fu Qi, Gu Yong, Shi Yun, Zhang Mei, Sun Min, Chen Heng, Han Xiuqun, Li Yangxi, Tang Zhoukai, Cai Lejing, Li Zhiqiang, Shi Yongyong, Yang Tao, Polychronakos Constant |
| Malignant transformation of liver fatty acid binding protein-deficient hepatocellular adenomas: histopathologic spectrum of a rare phenomenon. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 Sep . Putra Juan, Ferrell Linda D, Gouw Annette S H, Paradis Valerie, Rishi Arvind, Sempoux Christine, Balabaud Charles, Thung Swan N, Bioulac-Sage Paulet |
Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study.
PloS one 2019 14 (10): e0223574. Best Lyle G, Balakrishnan Poojitha, Cole Shelley A, Haack Karin, Kocarnik Jonathan M, Pankratz Nathan, Anderson Matthew Z, Franceschini Nora, Howard Barbara V, Lee Elisa T, North Kari E, Umans Jason G, Yracheta Joseph M, Navas-Acien Ana, Voruganti V Saro |
| Next generation sequencing targeted gene panel in Greek MODY patients increases diagnostic accuracy. Pediatric diabetes 2019 10 21 (1): 28-39. Tatsi Elizabeth B, Kanaka-Gantenbein Christina, Scorilas Andreas, Chrousos George P, Sertedaki Amal |
| Analysis of the promoter regions of disease-causing genes in maturity-onset diabetes of the young patients. Molecular biology reports 2020 8 47 (9): 6759-6768. Komazec Jovana, Ristivojevic Bojan, Zukic Branka, Zdravkovic Vera, Karan-Djurasevic Teodora, Pavlovic Sonja, Ugrin Mile |
| Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population. Medicina (Kaunas, Lithuania) 2020 8 56 (9): . Rodríguez-Arellano Martha Eunice, Solares-Tlapechco Jacqueline, Costa-Urrutia Paula, Cárdenas-Hernández Helios, Vallejo-Gómez Marajael, Granados Julio, Salas-Padilla Serg |
| Identification of the First PAX4-MODY Family Reported in Brazil. Diabetes, metabolic syndrome and obesity : targets and therapy 2020 8 13 2623-2631. Abreu Gabriella de Medeiros, Soares Camila de Almeida Pereira Dias, Tarantino Roberta Magalhães, da Fonseca Ana Carolina Proença, de Souza Ritiele Bastos, Pereira Maria de Fátima Carvalho, Cabello Pedro Hernan, Rodacki Melanie, Zajdenverg Lenita, Zembrzuski Verônica Marques, Campos Junior Már |
| Identification of Genetic Variants Associated With Myocardial Infarction in Saudi Arabia. The heart surgery forum 2020 Jul 23 (4): E517-E523. Ai-Ghalayini Kamal W, Salama Mohammed A, Al Mahdi Hadia Bassam, Al-Harthi Sameer, Alhejily Wesam A, Alasnag Mirvat A, Tasbhji Noura O, Al-Quwaie Diana A H, Deloukas Panos, Edris Sher |
| Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke.
Stroke 2020 Aug 51 (8): 2454-2463. Keene Keith L, Hyacinth Hyacinth I, Bis Joshua C, Kittner Steven J, Mitchell Braxton D, Cheng Yu-Ching, Pare Guillaume, Chong Michael, O'Donnell Martin, Meschia James F, Chen Wei-Min, Sale Michèle M, Rich Stephen S, Nalls Mike A, Zonderman Alan B, Evans Michele K, Wilson James G, Correa Adolfo, Markus Hugh S, Traylor Matthew, Lewis Cathryn M, Carty Cara L, Reiner Alexander, Haessler Jeff, Langefeld Carl D, Gottesman Rebecca, Mosley Thomas H, Woo Daniel, Yaffe Kristine, Liu YongMei, Longstreth William T, Psaty Bruce M, Kooperberg Charles, Lange Leslie A, Sacco Ralph, Rundek Tatjana, Lee Jin-Moo, Cruchaga Carlos, Furie Karen L, Arnett Donna K, Benavente Oscar R, Grewal Raji P, Peddareddygari Leema Reddy, Dichgans Martin, Malik Rainer, Worrall Bradford B, Fornage Myriam, |
| A study of associations between CUBN, HNF1A, and LIPC gene polymorphisms and coronary artery disease. Scientific reports 2020 10 10 (1): 16294. Park Han Sung, Kim In Jai, Kim Eun Gyo, Ryu Chang Soo, Lee Jeong Yong, Ko Eun Ju, Park Hyeon Woo, Sung Jung Hoon, Kim Nam Ke |
| Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the CEL Gene. Advanced biomedical research 2020 9 25. Sarmadi Akram, Mohammadi Aliasgar, Tabatabaei Fatemeh, Nouri Zahra, Chaleshtori Morteza Hashemzadeh, Tabatabaiefar Mohammad Am |
| Genome-wide association of individual vulnerability with alcohol-associated liver disease: A Korean genome and epidemiology study.
Hepatology (Baltimore, Md.) 2021 Aug . Kim Kwang Yoon, Kim Jung Oh, Kim Young-Sang, Choi Ja-Eun, Park Jae-Min, Han Kunhee, Park Da-Hyun, Park Yon Chul, Kim Bom Taeck, Hong Kyung-W |
| Analysis of rare coding variants in 200,000 exome-sequenced subjects reveals novel genetic risk factors for type 2 diabetes. Diabetes/metabolism research and reviews 2021 Jul e3482. Curtis Dav |
| Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders. The Journal of clinical endocrinology and metabolism 2021 Mar . Vishnopolska Sebastian Alexis, Mercogliano Maria Florencia, Camilletti Maria Andrea, Mortensen Amanda Helen, Braslavsky Debora, Keselman Ana, Bergadá Ignacio, Olivieri Federico, Miranda Lucas, Marino Roxana, Ramírez Pablo, Pérez Garrido Natalia, Patiño Mejia Helen, Ciaccio Marta, Di Palma Maria Isabel, Belgorosky Alicia, Martí Marcelo Adrian, Kitzman Jacob Otto, Camper Sally Ann, Pérez-Millán Maria In |
| Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes. Scientific reports 2021 Nov 11 (1): 21565. Deaton Aimee M, Parker Margaret M, Ward Lucas D, Flynn-Carroll Alexander O, BonDurant Lucas, Hinkle Gregory, Akbari Parsa, Lotta Luca A, , , Baras Aris, Nioi Pa |
| Polymorphisms in Genes of Lipid Metabolism Are Associated with Type 2 Diabetes Mellitus and Periodontitis, as Comorbidities, and with the Subjects' Periodontal, Glycemic, and Lipid Profiles. Journal of diabetes research 2021 11 2021 1049307. Nicchio Ingra G, Cirelli Thamiris, Nepomuceno Rafael, Hidalgo Marco A R, Rossa Carlos, Cirelli Joni A, Orrico Silvana R P, Barros Silvana P, Theodoro Letícia H, Scarel-Caminaga Raquel |
| Association of type 2 diabetes mellitus and periodontal disease susceptibility with genome-wide association-identified risk variants in a Southeastern Brazilian population. Clinical oral investigations 2021 Jan . Cirelli Thamiris, Nepomuceno Rafael, Goveia Jéssica Marina, Orrico Silvana R P, Cirelli Joni A, Theodoro Letícia Helena, Barros Silvana P, Scarel-Caminaga Raquel |
| Variants influencing age at diagnosis of HNF1A-MODY. Molecular medicine (Cambridge, Mass.) 2022 9 28 (1): 113. Ludwig-S?omczy?ska Agnieszka H, Seweryn Micha? T, Radkowski Piotr, Kapusta Przemys?aw, Machlowska Julita, Pruhova Stepanka, Gasperikova Daniela, Bellanne-Chantelot Christine, Hattersley Andrew, Kandasamy Balamurugan, Letourneau-Freiberg Lisa, Philipson Louis, Doria Alessandro, Wo?kow Pawe? P, Ma?ecki Maciej T, Klupa Toma |
| Early-onset diabetes involving three consecutive generations had different clinical features from age-matched type 2 diabetes without a family history in China. Endocrine 2022 Oct 78 (1): 47-56. Wang Da-Wei, Yuan Jing, Yang Fang-Yuan, Qiu Hai-Yan, Lu Jing, Yang Jin-K |
| Meta-analysis of HNF1A-MODY3 variants among human population. Journal of diabetes and metabolic disorders 2022 Jun 21 (1): 1037-1046. Behl Rachna, Malhotra Nishtha, Joshi Vinay, Poojary Shruti, Middha Sanniya, Gupta Shalini, Olaonipekun Arinola B, Okoye Ikechukwu, Wagh Bhushan, Biswas Dibyendu, Aginah Chukwuemelie, Saini Bhavya, Nwanya Chinaza, Ugwu Sopuluchukwu, Anthony Modupe M, Fang Xuanyu S, Foluso Ogunfile, Ibrahim Abdulrahman Tu |
| Identification of Variants Responsible for Monogenic Forms of Diabetes in Brazil. Frontiers in endocrinology 2022 5 13 827325. Abreu Gabriella de Medeiros, Tarantino Roberta Magalhães, da Fonseca Ana Carolina Proença, Andrade Juliana Rosa Ferreira de Oliveira, de Souza Ritiele Bastos, Soares Camila de Almeida Pereira Dias, Cambraia Amanda, Cabello Pedro Hernan, Rodacki Melanie, Zajdenverg Lenita, Zembrzuski Verônica Marques, Campos Junior Már |
| Monogenic diabetes variants in Emirati women with gestational diabetes are associated with risk of non-autoimmune diabetes within 5 years after pregnancy. Metabolism open 2022 11 16 100213. Daggag Hinda, Gjesing Anette P, Mohammad Alshafi, Ängquist Lars, Shobi Bindu, Antony Suma, Haj Dalia, Al Tikriti Alia, Buckley Adam, Hansen Torben, Barakat Maha |
| Reduced penetrance of MODY-associated HNF1A/HNF4A variants but not GCK variants in clinically unselected cohorts. American journal of human genetics 2022 10 109 (11): 2018-2028. Mirshahi Uyenlinh L, Colclough Kevin, Wright Caroline F, Wood Andrew R, Beaumont Robin N, Tyrrell Jessica, Laver Thomas W, Stahl Richard, Golden Alicia, Goehringer Jessica M, , Frayling Timothy F, Hattersley Andrew T, Carey David J, Weedon Michael N, Patel Kashyap |
| A novel splice-affecting HNF1A variant with large population impact on diabetes in Greenland. The Lancet regional health. Europe 2023 1 24 100529. Thuesen Anne Cathrine Baun, Stæger Frederik Filip, Kaci Alba, Solheim Marie Holm, Aukrust Ingvild, Jørsboe Emil, Santander Cindy G, Andersen Mette K, Li Zilong, Gilly Arthur, Stinson Sara Elizabeth, Gjesing Anette Prior, Bjerregaard Peter, Pedersen Michael Lynge, Larsen Christina Viskum Lytken, Grarup Niels, Jørgensen Marit E, Zeggini Eleftheria, Bjørkhaug Lise, Njølstad Pål Rasmus, Albrechtsen Anders, Moltke Ida, Hansen Torb |
| Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran. Scientific reports 2024 8 14 (1): 19860. Sara Asgarian, Hossein Lanjanian, Shiva Rahimipour Anaraki, Farzad Hadaegh, Maryam Moazzam-Jazi, Leila Najd-Hassan-Bonab, Sajedeh Masjoudi, Asiyeh Sadat Zahedi, Maryam Zarkesh, Bita Shalbafan, Mahdi Akbarzadeh, Sahand Tehrani Fateh, Davood Khalili, Amirabbas Momenan, Narges Sarbazi, Mehdi Hedayati, Fereidoun Azizi, Maryam S Daneshpo |
| Genetic insights into fetal kidney development: Variants in HNF1A and PKHD1 genes. Gene 2024 6 148625. Mayssa Abdelwahed, Valerie Benoit, Bayen Maalej, Pascale Hilbert, Laurence Michel Calemard, Hassen Kamoun, Leila Ammar-Keskes, Neila Belgui |
| Monogenic diabetes in a Chinese population with young-onset diabetes: A 17-year prospective follow-up study in Hong Kong. Diabetes/metabolism research and reviews 2024 5 40 (5): e3823. Sandra T F Tsoi, Cadmon Lim, Ronald C W Ma, Eric S H Lau, Baoqi Fan, Elaine Chow, Alice P S Kong, Juliana C N Chan, Andrea O Y L |
| Diagnostic yield of exome and genome sequencing after non-diagnostic multi-gene panels in patients with single-system diseases. Orphanet journal of rare diseases 2024 5 19 (1): 216. Matheus V M B Wilke, Eric W Klee, Radhika Dhamija, Fernando C Fervenza, Brittany Thomas, Nelson Leung, Marie C Hogan, Megan M Hager, Kayla J Kolbert, Jennifer L Kemppainen, Elle C Loftus, Katie M Leitzen, Carolyn R Vitek, Tammy McAllister, Konstantinos N Lazaridis, Filippo Pinto E Vai |
| GWAS of CRP response to statins further supports the role of APOE in statin response: A GIST consortium study. Pharmacological research 2025 1 212 107575. Emma F Magavern, Harshal Deshmukh, Geraldine Asselin, Elizabeth Theusch, Stella Trompet, Xiaohui Li, Raymond Noordam, Y-D Ida Chen, Teresa E Seeman, Kent D Taylor, Wendy S Post, Jean-Claude Tardif, Dirk S Paul, Emelia J Benjamin, Nancy L Heard-Costa, Ramachandran S Vasan, Jerome I Rotter, Ronald M Krauss, J Wouter Jukema, Paul M Ridker, Patricia B Munroe, Mark J Caulfield, Daniel I Chasman, Marie-Pierre Dubé, Graham A Hitman, Helen R Warren, |
- Page last reviewed:Feb 1, 2024
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