Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 260 Records) |
Query Trace: GCK[original query] |
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Study of the frequency and clinical features of maturity-onset diabetes in the young in the pediatric and adolescent diabetes population in Iran. Journal of pediatric endocrinology & metabolism : JPEM 2022 9 35 (10): 1240-1249. Zamanfar Daniel, Ferdosipour Fatemeh, Ebrahimi Pirooz, Moghadam Mohamad, Amoli Mahsa M, Asadi Mojgan, Monajati Mahi |
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 |
Monogenic diabetes in adults: A multi-ancestry study reveals strong disparities in diagnosis rates and clinical presentation. Diabetes research and clinical practice 2022 5 188 109908. Mifsud F, Saint-Martin C, Dubois-Laforgue D, Bouvet D, Timsit J, Bellanné-Chantelot C, |
Achievements, prospects and challenges in precision care for monogenic insulin-deficient and insulin-resistant diabetes. Diabetologia 2022 5 65 (11): 1782-1795. Bonnefond Amélie, Semple Robert |
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 |
Genetic Variants of Glycogen Metabolism Genes Were Associated With Liver PDFF Without Increasing NAFLD Risk. Frontiers in genetics 2022 4 13 830445. Yang Liu, Sun Zewen, Li Jiuling, Pan Xingchen, Wen Jianping, Yang Jianli, Wang Qing, Chen Pe |
Genetic and clinical features of neonatal and early onset diabetes mellitus in a tertiary center cohort in Brazil. Clinical genetics 2022 12 . Costa-Riquetto Aline Dantas, de Santana Lucas Santos, Franco Pedro Campos, Jr Augusto Cezar Santomauro, Martio Artur Eduardo, Lisboa Hugo Roberto Kurtz, Kohara Suely Keiko, Teles Milena |
Targeted gene panel analysis of Japanese patients with maturity-onset diabetes of the young-like diabetes mellitus: Roles of inactivating variants in the ABCC8 and insulin resistance genes. Journal of diabetes investigation 2022 12 . Yorifuji Tohru, Watanabe Yoh, Kitayama Kana, Yamada Yuki, Higuchi Shinji, Mori Jun, Kato Masaru, Takahashi Toru, Okuda Tokuko, Aoyama Taka |
A Novel GCK Large Genomic Rearrangement in a Patient with MODY-2 Detected by Clinical Exome Sequencing. Genes 2022 11 13 (11): . Concolino Paola, Tartaglione Linda, De Paolis Elisa, Carrozza Cinzia, Urbani Andrea, Minucci Angelo, Pitocco Dario, Santonocito Concet |
Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register. Diabetologia 2022 11 66 (3): 438-449. Harsunen Minna, Kettunen Jarno L T, Härkönen Taina, Dwivedi Om, Lehtovirta Mikko, Vähäsalo Paula, Veijola Riitta, Ilonen Jorma, Miettinen Päivi J, Knip Mikael, Tuomi Tiinamai |
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 |
14-fold increased prevalence of rare glucokinase gene variant carriers in unselected Danish patients with newly diagnosed type 2 diabetes. Diabetes research and clinical practice 2022 11 194 110159. Gjesing Anette P, Engelbrechtsen Line, Cathrine B Thuesen Anne, Have Christian T, Hollensted Mette, Grarup Niels, Linneberg Allan, Steen Nielsen Jens, Christensen Lotte B, Thomsen Reimar W, Johansson Kristoffer E, Cagiada Matteo, Gersing Sarah, Hartmann-Petersen Rasmus, Lindorff-Larsen Kresten, Vaag Allan, Sørensen Henrik T, Brandslund Ivan, Beck-Nielsen Henning, Pedersen Oluf, Rungby Jørgen, Hansen Torb |
Neonatal and early-onset diabetes in Ukraine: Atypical features and mortality. Diabetic medicine : a journal of the British Diabetic Association 2022 11 e15013. Globa Evgenia, Zelinska Nataliya, Johnson Matthew B, Flanagan Sarah E, De Franco Eli |
An effective preselection criterion for MODY with an increasingly positive genetic testing rate by NGS: results from two cohorts of Chinese children. American journal of physiology. Endocrinology and metabolism 2022 11 323 (6): E529-E534. Cao Bingyan, Liu Meijuan, Zhang Yingxian, Chen Jiajia, Li Xiaoqiao, Su Chang, Yang Wei, Liu Min, Wu Di, Li Wenjing, Liang Xuejun, Wang Qiao, Wei Haiyan, Gong Chunx |
Maturity-onset diabetes of the young in a large Portuguese cohort. Acta diabetologica 2022 Oct . Santos Monteiro Sílvia, da Silva Santos Tiago, Fonseca Liliana, Assunção Guilherme, Lopes Ana M, Duarte Diana B, Soares Ana Rita, Laranjeira Francisco, Ribeiro Isaura, Pinto Eugénia, Rocha Sónia, Barbosa Gouveia Sofia, Vazquez-Mosquera María Eugenia, Oliveira Maria João, Borges Teresa, Cardoso Maria Hele |
Statistical evidence for high-penetrance MODY-causing genes in a large population-based cohort. Endocrinology, diabetes & metabolism 2022 Oct e372. Billings Liana K, Shi Zhuqing, Resurreccion W Kyle, Wang Chi-Hsiung, Wei Jun, Pollin Toni I, Udler Miriam S, Xu Jianfe |
Hemoglobin A can differentiate subjects with GCK mutations among patients suspected to have MODY. Journal of pediatric endocrinology & metabolism : JPEM 2022 10 35 (12): 1528-1536. Y?lmaz Uzman Ceren, Erba? ?brahim Mert, Giray Bozkaya Özlem, Paketçi Ahu, Ça?layan Ahmet Okay, Abac? Ayhan, Kulal? Melike Ataseven, Böber Ece, Kekilli Arda, Çinleti Tayfun, Erçal Murat Derya, Demir Korc |
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 |
GCKR and GCK polymorphisms are associated with increased risk of end-stage kidney disease in Chinese patients with type 2 diabetes: The Hong Kong Diabetes Register (1995-2019). Diabetes research and clinical practice 2022 Oct 193 110118. Wang Ke, Shi Mai, Yang Aimin, Fan Baoqi, Tam Claudia H T, Lau Eric, Luk Andrea O Y, Kong Alice P S, Ma Ronald C W, Chan Juliana C N, Chow Elai |
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program.
Communications biology 2022 7 5 (1): 756. DiCorpo Daniel, Gaynor Sheila M, Russell Emily M, Westerman Kenneth E, Raffield Laura M, Majarian Timothy D, Wu Peitao, Sarnowski Chloé, Highland Heather M, Jackson Anne, Hasbani Natalie R, de Vries Paul S, Brody Jennifer A, Hidalgo Bertha, Guo Xiuqing, Perry James A, O'Connell Jeffrey R, Lent Samantha, Montasser May E, Cade Brian E, Jain Deepti, Wang Heming, D'Oliveira Albanus Ricardo, Varshney Arushi, Yanek Lisa R, Lange Leslie, Palmer Nicholette D, Almeida Marcio, Peralta Juan M, Aslibekyan Stella, Baldridge Abigail S, Bertoni Alain G, Bielak Lawrence F, Chen Chung-Shiuan, Chen Yii-Der Ida, Choi Won Jung, Goodarzi Mark O, Floyd James S, Irvin Marguerite R, Kalyani Rita R, Kelly Tanika N, Lee Seonwook, Liu Ching-Ti, Loesch Douglas, Manson JoAnn E, Minster Ryan L, Naseri Take, Pankow James S, Rasmussen-Torvik Laura J, Reiner Alexander P, Reupena Muagututi'a Sefuiva, Selvin Elizabeth, Smith Jennifer A, Weeks Daniel E, Xu Huichun, Yao Jie, Zhao Wei, Parker Stephen, Alonso Alvaro, Arnett Donna K, Blangero John, Boerwinkle Eric, Correa Adolfo, Cupples L Adrienne, Curran Joanne E, Duggirala Ravindranath, He Jiang, Heckbert Susan R, Kardia Sharon L R, Kim Ryan W, Kooperberg Charles, Liu Simin, Mathias Rasika A, McGarvey Stephen T, Mitchell Braxton D, Morrison Alanna C, Peyser Patricia A, Psaty Bruce M, Redline Susan, Shuldiner Alan R, Taylor Kent D, Vasan Ramachandran S, Viaud-Martinez Karine A, Florez Jose C, Wilson James G, Sladek Robert, Rich Stephen S, Rotter Jerome I, Lin Xihong, Dupuis Josée, Meigs James B, Wessel Jennifer, Manning Alisa |
The Association between CDKAL1 Gene rs10946398 Polymorphism and Post-Transplant Diabetes in Kidney Allograft Recipients Treated with Tacrolimus. Genes 2023 8 14 (8): . Violetta Dziedziejko, Krzysztof Safranow, Miros?awa Kijko-Nowak, Jerzy Sie?ko, Damian Malinowski, Kamila Szumilas, Andrzej Pawl |
The maternal and infant outcomes in GCK-MODY complicated with pregnancy: Systemic review and meta-analysis. The Journal of clinical endocrinology and metabolism 2023 4 . Ren Qian, Wang Zhihui, Yang Wenjia, Han Xueyao, Ji Lino |
Identification of pathogenic GCK variants in patients with common type 2 diabetes can lead to discontinuation of pharmacological treatment. Molecular genetics and metabolism reports 2023 4 35 100972. Thuesen Anne Cathrine Baun, Jensen Rasmus Tanderup, Maagensen Henrik, Kristiansen Maja Refshauge, Sørensen Henrik Toft, Vaag Allan, Beck-Nielsen Henning, Pedersen Oluf B, Grarup Niels, Nielsen Jens Steen, Rungby Jørgen, Gjesing Anette Prior, Storgaard Heidi, Vilsbøll Tina, Hansen Torb |
Prevalence, clinical features and complications of common forms of Maturity Onset Diabetes of the Young (MODY) seen at a tertiary diabetes centre in south India. Primary care diabetes 2023 4 . Aarthy Ramasamy, Aston-Mourney Kathryn, Amutha Anandakumar, Mikocka-Walus Antonina, Anjana Ranjit Mohan, Unnikrishnan Ranjit, Jebarani Saravanan, Venkatesan Ulagamathesan, Gopi Sundaramoorthy, Radha Venkatesan, Mohan Viswanath |
"Pesto" Mutation: Phenotypic and Genotypic Characteristics of Eight GCK/MODY Ligurian Patients. International journal of molecular sciences 2023 2 24 (4): . Salina Alessandro, Bassi Marta, Aloi Concetta, Strati Marina Francesca, Bocciardi Renata, d'Annunzio Giuseppe, Maghnie Mohamad, Minuto Nico |
Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus. Journal of clinical research in pediatric endocrinology 2023 12 . Enver ?im?ek, Oguz Cilingir, Tulay Simsek, Sinem Kocagil, Ebru Erzurumluoglu Gokalp, Meliha Demiral, Cigdem Bin |
Genotype-phenotype correlation in Taiwanese children with diazoxide-unresponsive congenital hyperinsulinism. Frontiers in endocrinology 2023 11 14 1283907. Cheng-Ting Lee, Wen-Hao Tsai, Chien-Ching Chang, Pei-Chun Chen, Cathy Shen-Jang Fann, Hsueh-Kai Chang, Shih-Yao Liu, Mu-Zon Wu, Pao-Chin Chiu, Wen-Ming Hsu, Wei-Shiung Yang, Ling-Ping Lai, Wen-Yu Tsai, Shi-Bing Yang, Pei-Lung Ch |
MOLECULAR DIAGNOSIS IN PATIENTS WITH MONOGENIC DIABETES MELLITUS, AND DETECTION OF A NOVEL CANDIDATE GENE. Diabetes research and clinical practice 2023 10 110953. Damla Goksen, Ferda Evin, Esra Isik, Samim Ozen, Tahir Atik, Ferda Ozkinay, Nese Akcan, Behzat Ozkan, Muammer Buyukinan, Mehmet Nuri Ozbek, Sukran Darcan, Huseyin On |
Association of GCK (rs1799884), GCKR (rs780094), and G6PC2 (rs560887) Gene Polymorphisms with Type 2 Diabetes among Malay Ethnics. Global medical genetics 2023 1 10 (1): 12-18. Ansari Neda, Ramachandran Vasudevan, Mohamad Nur Afiqah, Salim Elnaz, Ismail Patimah, Hazmi Mohamad, Mat Liyana Najwa Inch |
A Genome-Wide Association Study of Metabolic Syndrome in the Taiwanese Population. Nutrients 2024 1 16 (1): . Chih-Yi Ho, Jia-In Lee, Shu-Pin Huang, Szu-Chia Chen, Jiun-Hung Ge |
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- Page last updated:Apr 22, 2024
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