Works matching DE "GENETICS of diabetes"

Results: 949

Gut Bacteria May Override Genetic Protections against Diabetes.

Published in:

PLoS Biology, 2011, v. 9, n. 12, p. 1, doi. 10.1371/journal.pbio.1001215

By:

Meadows, Robin

Publication type:

Article

KDSNP: A kernel-based approach to detecting high-order SNP interactions.

Published in:

Journal of Bioinformatics & Computational Biology, 2016, v. 14, n. 5, p. -1, doi. 10.1142/S0219720016440030

By:

Kodama, Kento;
Saigo, Hiroto

Publication type:

Article

Does ancestry influence health-related quality of life in type 1 diabetes patients? A nationwide study in Brazil.

Published in:

Acta Diabetologica, 2018, v. 55, n. 4, p. 377, doi. 10.1007/s00592-017-1096-5

By:

Santos, Deborah Conte;
Pizarro, Marcela Haas;
Barros, Bianca S. V.;
de Melo, Laura G. Nunes;
Porto, Luis Cristovão;
Silva, Dayse A.;
Gomes, Marilia Brito

Publication type:

Article

The effect of a single dose of vitamin D on glycemic status and C-reactive protein levels in type 2 diabetic patients with ischemic heart disease: a randomized clinical trial.

Published in:

Acta Diabetologica, 2016, v. 53, n. 4, p. 575, doi. 10.1007/s00592-016-0843-3

By:

Shaseb, E.;
Tohidi, M.;
Abbasinazari, M.;
Khalili, D.;
Talasaz, A.;
Omrani, H.;
Hadaegh, F.

Publication type:

Article

A single-nucleotide polymorphism in the MicroRNA- 146a gene is associated with diabetic nephropathy and sight-threatening diabetic retinopathy in Caucasian patients.

Published in:

Acta Diabetologica, 2016, v. 53, n. 4, p. 643, doi. 10.1007/s00592-016-0850-4

By:

Kaidonis, Georgia;
Gillies, Mark;
Abhary, Sotoodeh;
Liu, Ebony;
Essex, Rohan;
Chang, John;
Pal, Bishwanath;
Sivaprasad, Sobha;
Pefkianaki, Maria;
Daniell, Mark;
Lake, Stewart;
Petrovsky, Nikolai;
Hewitt, Alex;
Jenkins, Alicia;
Lamoureux, Ecosse;
Gleadle, Jonathan;
Craig, Jamie;
Burdon, Kathryn

Publication type:

Article

Variation in the c heckpoint kinase 2 gene is associated with type 2 diabetes in multiple populations.

Published in:

Acta Diabetologica, 2010, v. 47, p. 199, doi. 10.1007/s00592-009-0162-z

By:

North, Kari E.;
Franceschini, Nora;
Avery, Christy L.;
Baird, Lisa;
Graff, Mariaelisa;
Leppert, Mark;
Chung, Jay H.;
Jinghui Zhang;
Hanis, Craig;
Boerwinkle, Eric;
Volcik, Kelly A.;
Grove, Megan L.;
Mosley, Thomas H.;
Gu, Charles;
Heiss, Gerardo;
Pankow, James S.;
Couper, David J.;
Ballantyne, Christie M.;
Linda Kao, W. H.;
Weder, Alan B.

Publication type:

Article

Outcome of pregnancy in type 1 diabetic patients treated with insulin lispro or regular insulin: an Italian experience.

Published in:

Acta Diabetologica, 2008, v. 45, n. 1, p. 61, doi. 10.1007/s00592-008-0024-0

By:

Lapolla, Annunziata;
Dalfrà, M. G.;
Spezia, R.;
Anichini, R.;
Bonomo, M.;
Bruttomesso, D.;
Di Cianni, G.;
Franzetti, I.;
Galluzzo, A.;
Mello, G.;
Menato, G.;
Napoli, A.;
Noacco, G.;
Parretti, E.;
Santini, C.;
Scaldaferri, E.;
Scaldaferri, L.;
Songini, M.;
Tonutti, L.;
Torlone, E.

Publication type:

Article

Clinical and genetic features of childhood-onset Type 2 diabetes in Japan.

Published in:

Acta Diabetologica, 2007, v. 44, n. 4, p. 181, doi. 10.1007/s00592-007-0002-y

By:

Otabe, Shuichi;
Nakayama, Hitomi;
Fukutani, Tomoka;
Xiaohong Yuan;
Wada, Nobuhiko;
Hashinaga, Toshihiko;
Kato, Tomoko;
Inada, Chizuko;
Yamada, Kentaro

Publication type:

Article

Screening for identifying individuals at risk of developing type 2 diabetes using the Canadian diabetes risk (CANRISK) questionnaire.

Published in:

Journal of Public Health: From Theory to Practice (2198-1833), 2023, v. 31, n. 6, p. 985, doi. 10.1007/s10389-021-01606-x

By:

Zairina, Elida;
Sulistyarini, Arie;
Nugraheni, Gesnita;
Kurnia Saputri, Sindy Irvana;
Permatasari, Ayudika;
Rachmawati, Elinda Eka

Publication type:

Article

Continuing hunt for diabetes genes targets unique mini-satellites.

Published in:: Nature, 1995, v. 374, n. 6517, p. 95
Publication type:: Article

A genome-wide search for human type 1 diabetes susceptibility genes.

Published in:

Nature, 1994, v. 371, n. 6493, p. 130, doi. 10.1038/371130a0

By:

Davies, June L.;
Kawaguchi, Yoshihiko

Publication type:

Article

Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q.

Published in:

Nature, 1994, v. 371, n. 6493, p. 161, doi. 10.1038/371161a0

By:

Hashimoto, L.;
Habita, C.

Publication type:

Article

Autoimmune diabetes as a consequence of locally produced interleukin-2.

Published in:

Nature, 1992, v. 359, n. 6395, p. 547, doi. 10.1038/359547a0

By:

Heath, William R.;
Allison, Janette

Publication type:

Article

Diabetes defect defined.

Published in:

Nature, 1992, v. 359, n. 6394, p. 434, doi. 10.1038/359434a0

By:

Davies, Kevin

Publication type:

Article

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin dependent diabetes...

Published in:

Nature, 1992, v. 356, n. 6365, p. 162, doi. 10.1038/356162a0

By:

Froguel, P.;
Vaxillaire, M.

Publication type:

Article

Psychiatric Pharmacogenetics: A Developing Science.

Published in:

Neuropsychopharmacology, 2002, v. 26, n. 1, p. 128, doi. 10.1016/S0893-133X(01)00377-3

By:

Berrettini, Wade

Publication type:

Article

Mapping of porcine genes related to human diabetes.

Published in:

2003

By:

Otieno, C.J.;
Vleck, S.;
Jelks, C.;
Kim, K.S.;
Nguyen, N.T.;
Rothschild, M.F.

Publication type:

Abstract

Transgenic mice with ectopic expression of constitutively active TLR4 in adipose tissues do not show impaired insulin sensitivity.

Published in:

Immunity, Inflammation & Disease, 2017, v. 5, n. 4, p. 526, doi. 10.1002/iid3.162

By:

Ono‐Moore, Kikumi D.;
Zhao, Ling;
Huang, Shurong;
Kim, Jeonga;
Rutkowsky, Jennifer M.;
Snodgrass, Ryan G.;
Schneider, Dina A.;
Quon, Michael J.;
Graham, James L.;
Havel, Peter J.;
Hwang, Daniel H.

Publication type:

Article

Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan.

Published in:

Pediatric Diabetes, 2024, v. 2024, p. 1, doi. 10.1155/2024/2032425

By:

Hassan, Samar S.;
Musa, Salwa A.;
De Franco, Elisa;
Donis Frew, Russel;
Babiker, Omer O.;
Mohamadsalih, Ghassan F.;
Ibrahim, Areej A.;
Abu Samra, Samar;
Abdullah, Mohamed A.

Publication type:

Article

Incidence Trends of Type 2 Diabetes Mellitus, Medication-Induced Diabetes, and Monogenic Diabetes in Canadian Children, Then (2006–2008) and Now (2017–2019).

Published in:

Pediatric Diabetes, 2023, p. 1, doi. 10.1155/2023/5511049

By:

Patel, Trisha J.;
Ayub, Aysha;
Bone, Jeffrey N.;
Hadjiyannakis, Stasia;
Henderson, Mélanie;
Nour, Munier A.;
Pinto, Teresa E.;
Wicklow, Brandy;
Hamilton, Jill K.;
Sellers, Elizabeth A. C.;
Amed, Shazhan

Publication type:

Article

ISPAD Clinical Practice Consensus Guidelines 2022: The diagnosis and management of monogenic diabetes in children and adolescents.

Published in:

Pediatric Diabetes, 2022, v. 23, n. 8, p. 1188, doi. 10.1111/pedi.13426

By:

Greeley, Siri Atma W.;
Polak, Michel;
Njølstad, Pål R.;
Barbetti, Fabrizio;
Williams, Rachel;
Castano, Luis;
Raile, Klemens;
Chi, Dung Vu;
Habeb, Abdelhadi;
Hattersley, Andrew T.;
Codner, Ethel

Publication type:

Article

Clinical presentation and long‐term outcome of patients with KCNJ11/ABCC8 variants: Neonatal diabetes or MODY in the DPV registry from Germany and Austria.

Published in:

Pediatric Diabetes, 2022, v. 23, n. 7, p. 999, doi. 10.1111/pedi.13390

By:

Warncke, Katharina;
Eckert, Alexander;
Kapellen, Thomas;
Kummer, Sebastian;
Raile, Klemens;
Dunstheimer, Desiree;
Grulich‐Henn, Jürgen;
Woelfle, Joachim;
Wenzel, Sandra;
Hofer, Sabine E.;
Dost, Axel;
Holl, Reinhard W.

Publication type:

Article

Case report: Neonatal diabetes mellitus with congenital hypothyroidism as a result of biallelic heterozygous mutations in GLIS3 gene.

Published in:

Pediatric Diabetes, 2022, v. 23, n. 6, p. 668, doi. 10.1111/pedi.13341

By:

Perdas, Ewelina;
Gadzalska, Karolina;
Hrytsiuk, Ihor;
Borowiec, Maciej;
Fendler, Wojciech;
Młynarski, Wojciech

Publication type:

Article

Clinical characteristics, growth patterns, and long‐term diabetes complications of 24 patients with neonatal diabetes mellitus: A single center experience.

Published in:

Pediatric Diabetes, 2022, v. 23, n. 1, p. 45, doi. 10.1111/pedi.13295

By:

Mouler, Marie;
Lebenthal, Yael;
de Vries, Liat;
Yackobovitch‐Gavan, Michal;
Averbuch, Noa Shefer;
Fauret‐Amsellem, Anne Laure;
Cavé, Helene;
Beltrand, Jacques;
Polak, Michel;
Phillip, Moshe;
Nimri, Revital

Publication type:

Article

Monogenic diabetes: A single center experience from South India.

Published in:

Pediatric Diabetes, 2021, v. 22, n. 1, p. 75, doi. 10.1111/pedi.13040

By:

Lakshmanan, Nivethitha Karthika;
Pavithran, Praveen V;
Bhavani, Nisha;
Abraham, Nithya;
Kumar, Harish;
Nair, Vasantha;
Menon, Usha;
Menon, Arun S;
Narayanan, Prem;
Lakshmi, Geetha

Publication type:

Article

Neonatal diabetes due to potassium channel mutation: Response to sulfonylurea according to the genotype.

Published in:

Pediatric Diabetes, 2020, v. 21, n. 6, p. 932, doi. 10.1111/pedi.13041

By:

Garcin, Laure;
Mericq, Veronica;
Fauret‐Amsellem, Anne‐Laure;
Cave, Helene;
Polak, Michel;
Beltrand, Jacques

Publication type:

Article

Five years of improving diabetes control in Czech children after the establishment of the population‐based childhood diabetes register ČENDA.

Published in:

Pediatric Diabetes, 2020, v. 21, n. 1, p. 77, doi. 10.1111/pedi.12929

By:

Šumník, Zdeněk;
Venháčová, Jitřenka;
Škvor, Jaroslav;
Pomahačová, Renata;
Konečná, Petra;
Neumann, David;
Vosáhlo, Jan;
Strnadel, Jiří;
Čížek, Jindřich;
Obermannová, Barbora;
Petruželková, Lenka;
Průhová, Štěpánka;
Pavlíková, Markéta;
Cinek, Ondřej

Publication type:

Article

Functional characterization of activating mutations in the sulfonylurea receptor 1 (ABCC8) causing neonatal diabetes mellitus in Asian Indian children.

Published in:

Pediatric Diabetes, 2019, v. 20, n. 4, p. 397, doi. 10.1111/pedi.12843

By:

Balamurugan, Kandasamy;
Kavitha, Babu;
Yang, Zhongying;
Mohan, Viswanathan;
Radha, Venkatesan;
Shyng, Show‐Ling

Publication type:

Article

Associations of growth from birth to puberty with glycemic indicators at ~17.5 years: Evidence from Hong Kong's "Children of 1997" birth cohort.

Published in:

Pediatric Diabetes, 2019, v. 20, n. 4, p. 380, doi. 10.1111/pedi.12838

By:

Cheng, Tuck Seng;
Leung, Gabriel M.;
Hui, Lai Ling;
Leung, June Yue Yan;
Kwok, Man Ki;
Au Yeung, Shiu Lun;
Schooling, C. Mary

Publication type:

Article

Phenotypic variability in two siblings with monogenic diabetes due to the same ABCC8 gene mutation.

Published in:

Pediatric Diabetes, 2019, v. 20, n. 4, p. 482, doi. 10.1111/pedi.12826

By:

Cattoni, Alessandro;
Jackson, Charlotte;
Bain, Murray;
Houghton, Jayne;
Wei, Christina

Publication type:

Article

Exome sequencing identifies a de novo FOXA2 variant in a patient with syndromic diabetes.

Published in:

Pediatric Diabetes, 2019, v. 20, n. 3, p. 366, doi. 10.1111/pedi.12814

By:

Stekelenburg, Caroline;
Schwitzgebel, Valerie M.;
Gerster, Karine;
Lang‐Muritano, Mariarosaria;
Blouin, Jean‐Louis;
Guipponi, Michel;
Santoni, Federico

Publication type:

Article

ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents.

Published in:

Pediatric Diabetes, 2018, v. 19, p. 47, doi. 10.1111/pedi.12772

By:

Hattersley, Andrew T.;
Greeley, Siri A. W.;
Polak, Michel;
Rubio‐Cabezas, Oscar;
Njølstad, Pål R.;
Mlynarski, Wojciech;
Castano, Luis;
Carlsson, Annelie;
Raile, Klemens;
Chi, Dung V.;
Ellard, Sian;
Craig, Maria E.

Publication type:

Article

A novel INS mutation in a family with maturity‐onset diabetes of the young: Variable insulin secretion and putative mechanisms.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 5, p. 905, doi. 10.1111/pedi.12679

By:

Johnson, Stephanie R.;
McGown, Ivan;
Oppermann, Udo;
Conwell, Louise S.;
Harris, Mark;
Duncan, Emma L.

Publication type:

Article

Permanent neonatal diabetes mellitus and neurological abnormalities due to a novel homozygous missense mutation in NEUROD1.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 5, p. 898, doi. 10.1111/pedi.12669

By:

Demirbilek, Huseyin;
Hatipoglu, Nihal;
Gul, Ulku;
Tatli, Zeynep U.;
Ellard, Sian;
Flanagan, Sarah E.;
De Franco, Elisa;
Kurtoglu, Selim

Publication type:

Article

Successful off‐label sulfonylurea treatment of neonatal diabetes mellitus due to chromosome 6 abnormalities.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 4, p. 663, doi. 10.1111/pedi.12635

By:

Garcin, Laure;
Kariyawasam, Dulanjalee;
Busiah, Kanetee;
Fauret‐Amsellem, Anne‐Laure;
Le Bourgeois, Fleur;
Vaivre‐Douret, Laurence;
Cavé, Hélène;
Polak, Michel;
Beltrand, Jacques

Publication type:

Article

Whole‐exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 4, p. 656, doi. 10.1111/pedi.12638

By:

Johnson, S. R.;
Leo, P. J.;
McInerney‐Leo, A. M.;
Anderson, L. K.;
Marshall, M.;
McGown, I.;
Newell, F.;
Brown, M. A.;
Conwell, L. S.;
Harris, M.;
Duncan, E. L.

Publication type:

Article

<italic>FOXP3</italic> mutations causing early‐onset insulin‐requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked syndrome.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 3, p. 388, doi. 10.1111/pedi.12612

By:

Hwang, Jessica L.;
Park, Soo‐Young;
Ye, Honggang;
Sanyoura, May;
Pastore, Ashley N.;
Carmody, David;
del Gaudio, Daniela;
Wilson, Janna F.;
Hanis, Craig L.;
Liu, Xiaoming;
Atzmon, Gil;
Glaser, Benjamin;
Philipson, Louis H.;
Greeley, Siri Atma W.;
T2D‐Genes Consortium

Publication type:

Article

Hypoglycemia in sulfonylurea‐treated KCNJ11‐neonatal diabetes: Mild‐moderate symptomatic episodes occur infrequently but none involving unconsciousness or seizures.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 3, p. 393, doi. 10.1111/pedi.12599

By:

Lanning, Monica S.;
Carmody, David;
Szczerbiński, Łukasz;
Letourneau, Lisa R.;
Naylor, Rochelle N.;
Greeley, Siri Atma W.

Publication type:

Article

A novel NEUROG3 mutation in neonatal diabetes associated with a neuro‐intestinal syndrome.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 3, p. 381, doi. 10.1111/pedi.12576

By:

Hancili, Suna;
Bonnefond, Amélie;
Philippe, Julien;
Vaillant, Emmanuel;
De Graeve, Franck;
Sand, Olivier;
Busiah, Kanetee;
Robert, Jean‐Jacques;
Polak, Michel;
Froguel, Philippe;
Güven, Ayla;
Vaxillaire, Martine

Publication type:

Article

NEUROD1‐deficient diabetes (MODY6): Identification of the first cases in Japanese and the clinical features.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 2, p. 236, doi. 10.1111/pedi.12553

By:

Horikawa, Yukio;
Enya, Mayumi;
Mabe, Hiroyo;
Fukushima, Kei;
Takubo, Noriyuki;
Ohashi, Masaaki;
Ikeda, Fuki;
Hashimoto, Ken‐ichi;
Watada, Hirotaka;
Takeda, Jun

Publication type:

Article

Monogenic diabetes prevalence among Polish children—Summary of 11 years‐long nationwide genetic screening program.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 1, p. 53, doi. 10.1111/pedi.12532

By:

Małachowska, Beata;
Borowiec, Maciej;
Antosik, Karolina;
Michalak, Arkadiusz;
Baranowska‐Jaźwiecka, Anna;
Deja, Grażyna;
Jarosz‐Chobot, Przemysława;
Brandt, Agnieszka;
Myśliwiec, Małgorzata;
Stelmach, Małgorzata;
Nazim, Joanna;
Peczyńska, Jadwiga;
Głowińska‐Olszewska, Barbara;
Horodnicka‐Józwa, Anita;
Walczak, Mieczysław;
Małecki, Maciej T.;
Zmysłowska, Agnieszka;
Szadkowska, Agnieszka;
Fendler, Wojciech;
Młynarski, Wojciech

Publication type:

Article

Definition, epidemiology, and classification of diabetes in children and adolescents.

Published in:

Pediatric Diabetes, 2014, v. 15, p. 4, doi. 10.1111/pedi.12186

By:

Craig, Maria E;
Jefferies, Craig;
Dabelea, Dana;
Balde, Naby;
Seth, Anju;
Donaghue, Kim C

Publication type:

Article

Permanent neonatal diabetes in siblings with novel C109Y INS mutation transmitted by an unaffected parent with somatic mosaicism.

Published in:

Pediatric Diabetes, 2014, v. 15, n. 4, p. 324, doi. 10.1111/pedi.12104

By:

Bee, Yong Mong;
Zhao, Yi;
Ellard, Sian;
Hattersley, Andrew T;
Yap, Fabian

Publication type:

Article

EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndrome.

Published in:

Pediatric Diabetes, 2014, v. 15, n. 4, p. 313, doi. 10.1111/pedi.12089

By:

Jahnavi, Suresh;
Poovazhagi, Varadarajan;
Kanthimathi, Sekar;
Gayathri, Vijay;
Mohan, Viswanathan;
Radha, Venkatesan

Publication type:

Article

Increased risk for overweight among Swedish children born to mothers with gestational diabetes mellitus.

Published in:

Pediatric Diabetes, 2014, v. 15, n. 1, p. 57, doi. 10.1111/pedi.12059

By:

Nilsson, Charlotta;
Carlsson, Annelie;
Landin‐Olsson, Mona

Publication type:

Article

Digenic heterozygous HNF1A and HNF4A mutations in two siblings with childhood-onset diabetes.

Published in:

Pediatric Diabetes, 2013, v. 14, n. 7, p. 535, doi. 10.1111/pedi.12018

By:

Shankar, Roopa Kanakatti;
Ellard, Sian;
Standiford, Debra;
Pihoker, Catherine;
Gilliam, Lisa K;
Hattersley, Andrew;
Dolan, Lawrence M

Publication type:

Article

Xanthomata and diabetes in an adolescent with familial dysbetalipoproteinemia 9 yr after valproate-induced pancreatitis.

Published in:

Pediatric Diabetes, 2012, v. 13, n. 5, p. 444, doi. 10.1111/j.1399-5448.2011.00843.x

By:

Jetha, Mary M;
Fiorillo, Loretta

Publication type:

Article

Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: treatment with sulfonylurea and 40-yr follow-up.

Published in:

Pediatric Diabetes, 2012, v. 13, n. 2, p. 155, doi. 10.1111/j.1399-5448.2011.00776.x

By:

Søvik, Oddmund;
Aagenæs, Øystein;
Eide, Stig Å;
Mackay, Deborah;
Temple, Isabel K;
Molven, Anders;
Njølstad, Pål R

Publication type:

Article

Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus.

Published in:

Pediatric Diabetes, 2012, v. 13, n. 1, p. 26, doi. 10.1111/j.1399-5448.2011.00827.x

By:

Yorifuji, Tohru;
Fujimaru, Rika;
Hosokawa, Yuki;
Tamagawa, Nobuyoshi;
Shiozaki, Momoko;
Aizu, Katsuya;
Jinno, Kazuhiko;
Maruo, Yoshihiro;
Nagasaka, Hironori;
Tajima, Toshihiro;
Kobayashi, Koji;
Urakami, Tatsuhiko

Publication type:

Article

The Environmental Determinants of Diabetes in the Young (TEDDY): genetic criteria and international diabetes risk screening of 421 000 infants.

Published in:

Pediatric Diabetes, 2011, v. 12, n. 8, p. 733, doi. 10.1111/j.1399-5448.2011.00774.x

By:

Hagopian, William A;
Erlich, Henry;
Lernmark, Åke;
Rewers, Marian;
Ziegler, Anette G;
Simell, Olli;
Akolkar, Beena;
Vogt, Robert;
Blair, Alan;
Ilonen, Jorma;
Krischer, Jeffrey;
She, JinXiong

Publication type:

Article