Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and NEUROD1[original query] |
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| NeuroD1 gene and interleukin-18 gene polymorphisms in type 1 diabetes in Dalmatian population of Southern Croatia. Croatian medical journal 2006 Aug 47 (4): 571-8. Boraska Vesna, Terzi? Janos, Skrabi? Veselin, Ca?ev Tamara, Bucevi?-Popovi? Viljemka, Peruzovi? Marijana, Markoti? Anita, Zemunik Tatija |
| 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 |
| 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 |
| 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, |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
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