Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 43 Records) |
Query Trace: NEUROD1[original query] |
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Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes. Diabetes 2007 Mar 56 (3): 685-93. Winckler Wendy, Weedon Michael N, Graham Robert R, McCarroll Steven A, Purcell Shaun, Almgren Peter, Tuomi Tiinamaija, Gaudet Daniel, Boström Kristina Bengtsson, Walker Mark, Hitman Graham, Hattersley Andrew T, McCarthy Mark I, Ardlie Kristin G, Hirschhorn Joel N, Daly Mark J, Frayling Timothy M, Groop Leif, Altshuler Dav |
Mutations of maturity-onset diabetes of the young (MODY) genes in Thais with early-onset type 2 diabetes mellitus. Clinical endocrinology 2009 Jun 70 (6): 847-53. Plengvidhya Nattachet, Boonyasrisawat Watip, Chongjaroen Nalinee, Jungtrakoon Prapaporn, Sriussadaporn Sutin, Vannaseang Sathit, Banchuin Napatawn, Yenchitsomanus Pa-th |
A-beta-subtype of ketosis-prone diabetes is not predominantly a monogenic diabetic syndrome. Diabetes care 2009 May 32 (5): 873-7. Haaland Wade C, Scaduto Diane I, Maldonado Mario R, Mansouri Dena L, Nalini Ramaswami, Iyer Dinakar, Patel Sanjeet, Guthikonda Anu, Hampe Christiane S, Balasubramanyam Ashok, Metzker Michael |
Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalities. Diabetes 2010 Sep 59 (9): 2326-31. Rubio-Cabezas Oscar, Minton Jayne A L, Kantor Iren, Williams Denise, Ellard Sian, Hattersley Andrew |
Retinopathy and nephropathy in type 1 diabetic patients--association with polymorphysms of vitamin D-receptor, TNF, Neuro-D and IL-1 receptor 1 genes. Collegium antropologicum 2009 Dec 33 Suppl 2 99-105. Bu?an Kajo, Ivanisevi? Milan, Zemunik Tatijana, Boraska Vesna, Skrabi? Veselin, Vatavuk Zoran, Galetovi? Davor, Znaor Lju |
Association of variants in genes involved in pancreatic ß-cell development and function with type 2 diabetes in North Indians. Journal of human genetics 2011 Oct 56 (10): 695-700. Chavali Sreenivas, Mahajan Anubha, Tabassum Rubina, Dwivedi Om Prakash, Chauhan Ganesh, Ghosh Saurabh, Tandon Nikhil, Bharadwaj Dwaipay |
NeuroD1 A45T and PAX4 R121W polymorphisms are associated with plasma glucose level of repaglinide monotherapy in Chinese patients with type 2 diabetes. British journal of clinical pharmacology 2012 Sep 74 (3): 501-9. Gong Zhi-Cheng, Huang Qiong, Dai Xing-Ping, Lei Guang-Hua, Lu Hong-Bin, Yin Ji-Ye, Xu Xiao-Jing, Qu Jian, Pei Qi, Dong Min, Zhou Bo-Ting, Shen Jie, Zhou Gan, Zhou Hong-Hao, Liu Zhao-Qi |
Evaluation of variant A45T in NEUROD1/BETA2 for its association with type 2 diabetes mellitus. Endocrine 2013 Aug 44 (1): 99-106. Han Xueyao, Xiao Jianzhong, Ren Qian, Tang Yong, Yang Wenying, Ji Lino |
Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing. Journal of pediatric endocrinology & metabolism : JPEM 2015 Jul . An?k Ahmet, Çatl? Gönül, Abac? Ayhan, Sar? Erkan, Ye?ilkaya Ediz, Korkmaz Hüseyin An?l, Demir Korcan, Alt?nc?k Ayça, Tuhan Hale Ünver, K?z?lda? Sefa, Özkan Behzat, Ceylaner Serdar, Böber E |
The role of transcription factors of neurosensory cells in non-syndromic sensorineural hearing loss with or without inner ear malformation. Acta oto-laryngologica 2015 Dec 1-6. Zhou Yuan, Qing Jie, Dong Yunpeng, Nie Jin, Li Jingkun, Wang Chunmei, Liu Yuyuan, Peng Tao, Duan Maoli, Liu Xuezhong, Xie Dingh |
Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing. Journal of pediatric endocrinology & metabolism : JPEM 2015 Dec . A?lad?o?lu Sebahat Y?lmaz, Aycan Zehra, Çetinkaya Semra, Ba? Veysel Nijat, Önder A?an, Peltek Kendirci Havva Nur, Do?an Haldun, Ceylaner Serd |
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nature genetics 2015 Nov . Gaulton Kyle J, Ferreira Teresa, Lee Yeji, Raimondo Anne, Mägi Reedik, Reschen Michael E, Mahajan Anubha, Locke Adam, William Rayner N, Robertson Neil, Scott Robert A, Prokopenko Inga, Scott Laura J, Green Todd, Sparso Thomas, Thuillier Dorothee, Yengo Loic, Grallert Harald, Wahl Simone, Frånberg Mattias, Strawbridge Rona J, Kestler Hans, Chheda Himanshu, Eisele Lewin, Gustafsson Stefan, Steinthorsdottir Valgerdur, Thorleifsson Gudmar, Qi Lu, Karssen Lennart C, van Leeuwen Elisabeth M, Willems Sara M, Li Man, Chen Han, Fuchsberger Christian, Kwan Phoenix, Ma Clement, Linderman Michael, Lu Yingchang, Thomsen Soren K, Rundle Jana K, Beer Nicola L, van de Bunt Martijn, Chalisey Anil, Kang Hyun Min, Voight Benjamin F, Abecasis Gonçalo R, Almgren Peter, Baldassarre Damiano, Balkau Beverley, Benediktsson Rafn, Blüher Matthias, Boeing Heiner, Bonnycastle Lori L, Bottinger Erwin P, Burtt Noël P, Carey Jason, Charpentier Guillaume, Chines Peter S, Cornelis Marilyn C, Couper David J, Crenshaw Andrew T, van Dam Rob M, Doney Alex S F, Dorkhan Mozhgan, Edkins Sarah, Eriksson Johan G, Esko Tonu, Eury Elodie, Fadista João, Flannick Jason, Fontanillas Pierre, Fox Caroline, Franks Paul W, Gertow Karl, Gieger Christian, Gigante Bruna, Gottesman Omri, Grant George B, Grarup Niels, Groves Christopher J, Hassinen Maija, Have Christian T, Herder Christian, Holmen Oddgeir L, Hreidarsson Astradur B, Humphries Steve E, Hunter David J, Jackson Anne U, Jonsson Anna, Jørgensen Marit E, Jørgensen Torben, Kao Wen-Hong L, Kerrison Nicola D, Kinnunen Leena, Klopp Norman, Kong Augustine, Kovacs Peter, Kraft Peter, Kravic Jasmina, Langford Cordelia, Leander Karin, Liang Liming, Lichtner Peter, Lindgren Cecilia M, Lindholm Eero, Linneberg Allan, Liu Ching-Ti, Lobbens Stéphane, Luan Jian'an, Lyssenko Valeriya, Männistö Satu, McLeod Olga, Meyer Julia, Mihailov Evelin, Mirza Ghazala, Mühleisen Thomas W, Müller-Nurasyid Martina, Navarro Carmen, Nöthen Markus M, Oskolkov Nikolay N, Owen Katharine R, Palli Domenico, Pechlivanis Sonali, Peltonen Leena, Perry John R B, Platou Carl G P, Roden Michael, Ruderfer Douglas, Rybin Denis, van der Schouw Yvonne T, Sennblad Bengt, Sigurðsson Gunnar, Stan?áková Alena, Steinbach Gerald, Storm Petter, Strauch Konstantin, Stringham Heather M, Sun Qi, Thorand Barbara, Tikkanen Emmi, Tonjes Anke, Trakalo Joseph, Tremoli Elena, Tuomi Tiinamaija, Wennauer Roman, Wiltshire Steven, Wood Andrew R, Zeggini Eleftheria, Dunham Ian, Birney Ewan, Pasquali Lorenzo, Ferrer Jorge, Loos Ruth J F, Dupuis Josée, Florez Jose C, Boerwinkle Eric, Pankow James S, van Duijn Cornelia, Sijbrands Eric, Meigs James B, Hu Frank B, Thorsteinsdottir Unnur, Stefansson Kari, Lakka Timo A, Rauramaa Rainer, Stumvoll Michael, Pedersen Nancy L, Lind Lars, Keinanen-Kiukaanniemi Sirkka M, Korpi-Hyövälti Eeva, Saaristo Timo E, Saltevo Juha, Kuusisto Johanna, Laakso Markku, Metspalu Andres, Erbel Raimund, Jöcke Karl-Heinz, Moebus Susanne, Ripatti Samuli, Salomaa Veikko, Ingelsson Erik, Boehm Bernhard O, Bergman Richard N, Collins Francis S, Mohlke Karen L, Koistinen Heikki, Tuomilehto Jaakko, Hveem Kristian, Njølstad Inger, Deloukas Panagiotis, Donnelly Peter J, Frayling Timothy M, Hattersley Andrew T, de Faire Ulf, Hamsten Anders, Illig Thomas, Peters Annette, Cauchi Stephane, Sladek Rob, Froguel Philippe, Hansen Torben, Pedersen Oluf, Morris Andrew D, Palmer Collin N A, Kathiresan Sekar, Melander Olle, Nilsson Peter M, Groop Leif C, Barroso Inês, Langenberg Claudia, Wareham Nicholas J, O'Callaghan Christopher A, Gloyn Anna L, Altshuler David, Boehnke Michael, Teslovich Tanya M, McCarthy Mark I, Morris Andrew P, |
Variation in Maturity-Onset Diabetes of the Young Genes Influence Response to Interventions for Diabetes Prevention. The Journal of clinical endocrinology and metabolism 2017 Apr . Billings Liana K, Jablonski Kathleen A, Warner A Sofia, Cheng Yu-Chien, McAteer Jarred B, Tipton Laura, Shuldiner Alan R, Ehrmann David A, Manning Alisa K, Dabelea Dana, Franks Paul W, Kahn Steven E, Pollin Toni I, Knowler William C, Altshuler David, Florez Jose C, |
Comprehensive Maturity Onset Diabetes of the Young (MODY) Gene Screening in Pregnant Women with Diabetes in India. PloS one 2017 1 12 (1): e0168656. Doddabelavangala Mruthyunjaya Mahesh, Chapla Aaron, Hesarghatta Shyamasunder Asha, Varghese Deny, Varshney Manika, Paul Johan, Inbakumari Mercy, Christina Flory, Varghese Ron Thomas, Kuruvilla Kurien Anil, V Paul Thomas, Jose Ruby, Regi Annie, Lionel Jessie, Jeyaseelan L, Mathew Jiji, Thomas Nih |
Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes. Journal of pediatric endocrinology & metabolism : JPEM 2019 6 32 (7): 759-765. Ming-Qiang Zhu, Yang-Li Dai, Ke Huang, Wei Wu, Jun-Fen Fu, Chao-Chun Zou, Guan-Ping Do |
Targeted sequencing identifies novel variants in common and rare MODY genes. Molecular genetics & genomic medicine 2019 10 7 (12): e962. de Santana Lucas S, Caetano Lilian A, Costa-Riquetto Aline D, Franco Pedro C, Dotto Renata P, Reis André F, Weinert Letícia S, Silveiro Sandra P, Vendramini Marcio F, do Prado Flaviene A, Abrahão Giovanna C P, de Almeida Ana Gregória F P, Tavares Maria da G Rodrigues, Gonçalves Wagner Rodrigo B, Santomauro Junior Augusto C, Halpern Bruno, Jorge Alexander A L, Nery Marcia, Teles Milena |
Identification of nucleotide polymorphism within the NeuroD1 candidate gene and its association with type 1 diabetes susceptibility in Iranian people by polymerase chain reaction-restriction fragment length polymorphism. Journal of pediatric endocrinology & metabolism : JPEM 2020 Aug . Soltani Asl Maryam, Azimnasab-Sorkhabi Parviz, Abolfathi Ali-Akbar, Hashemi Aghdam Yash |
Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience. Acta diabetologica 2021 8 58 (12): 1689-1700. Laimon Wafaa, El-Ziny Magdy, El-Hawary Amany, Elsharkawy Ashraf, Salem Nanees Abdel-Badie, Aboelenin Hadil Mohamed, Awad Mohammad Hosny, Flanagan Sarah E, De Franco Eli |
Neuronal Differentiation 1 gene Ala45Thr polymorphism and type 2 diabetes mellitus: A meta-analysis of 7,940 subjects. Nutrition, metabolism, and cardiovascular diseases : NMCD 2021 Mar . Li Yan-Yan, Wang Hui, Zhang Yang-Ya |
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. Journal of neurology 2021 1 268 (6): 2192-2207. Chakrabarty Sanjiban, Govindaraj Periyasamy, Sankaran Bindu Parayil, Nagappa Madhu, Kabekkodu Shama Prasada, Jayaram Pradyumna, Mallya Sandeep, Deepha Sekar, Ponmalar J N Jessiena, Arivinda Hanumanthapura R, Meena Angamuthu Kanikannan, Jha Rajan Kumar, Sinha Sanjib, Gayathri Narayanappa, Taly Arun B, Thangaraj Kumarasamy, Satyamoorthy Kapaet |
The Mutation Spectrum of Maturity Onset Diabetes of the Young (MODY)-Associated Genes among Western Siberia Patients. Journal of personalized medicine 2021 1 11 (1): . Ivanoshchuk Dinara E, Shakhtshneider Elena V, Rymar Oksana D, Ovsyannikova Alla K, Mikhailova Svetlana V, Fishman Veniamin S, Valeev Emil S, Orlov Pavel S, Voevoda Mikhail |
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 |
Prognosis prediction of stage IV colorectal cancer patients by mRNA transcriptional profile. Cancer medicine 2022 5 11 (24): 4900-4912. Wu Bian, Yang Jinwei, Qin Zhiwei, Yang Hongping, Shao Jingyi, Shang Y |
EXOC6 (Exocyst Complex Component 6) Is Associated with the Risk of Type 2 Diabetes and Pancreatic ?-Cell Dysfunction. Biology 2022 3 11 (3): . Sulaiman Nabil, Yaseen Hachim Mahmood, Khalique Anila, Mohammed Abdul Khader, Al Heialy Saba, Taneera Jal |
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 |
Role of monogenic diabetes genes on beta cell function in Italian patients with newly diagnosed type 2 diabetes. The Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 13. Diabetes & metabolism 2022 1 48 (4): 101323. Bonetti S, Zusi C, Rinaldi E, Boselli M L, Csermely A, Malerba G, Trabetti E, Bonora E, Bonadonna R C, Trombetta |
Evaluation of Type 2 Diabetes Risk Variants (Alleles) in the Pashtun Ethnic Population of Pakistan. Journal of the ASEAN Federation of Endocrine Societies 2023 5 38 (1): 48-54. Asif Jan, Muhammad Saeed, Zakiullah, Rani Akbar, Hamayun Kh |
Genetic variants of NEUROD1 target genes are associated with clinical outcomes of small-cell lung cancer patients. Thoracic cancer 2023 3 . Lee Sunwoong, Yoo Seung Soo, Choi Jin Eun, Hong Mi Jeong, Do Sook Kyung, Lee Jang Hyuck, Lee Won Ki, Park Ji Eun, Choi Sun Ha, Seo Hyewon, Lee Jaehee, Lee Shin Yup, Cha Seung Ick, Kim Chang Ho, Kang Hyo-Gyoung, Park Jae Yo |
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 |
Promoter-Specific Variants in NeuroD1 and H3K4me3 Coincident Regions and Clinical Outcomes of Small Cell Lung Cancer. Journal of Korean medical science 2023 11 38 (45): e381. Seung Soo Yoo, Sunwoong Lee, Jin Eun Choi, Mi Jeong Hong, Sook Kyung Do, Jang Hyuck Lee, Won Kee Lee, Ji Eun Park, Yong Hoon Lee, Sun Ha Choi, Hyewon Seo, Jaehee Lee, Shin Yup Lee, Seung Ick Cha, Chang Ho Kim, Hyo-Gyoung Kang, Jae Yong Pa |
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