Results 1 to 10 of about 735,632 (337)

Genetic epidemiology approach to estimating birth incidence and current disease prevalence for rhizomelic chondrodysplasia punctata. [PDF]

Orphanet J Rare Dis, 2021
Luisman T, Smith T, Ritchie S, Malone KE.   +3 more
europepmc   +3 more sources

Genetic epidemiology [PDF]

Journal of the Royal College of Physicians of Edinburgh, 2012
The field of genetic epidemiology has advanced considerably over the past decade. The falling costs of genome-wide association studies have allowed the identification of many common genetic variants associated with risk of illness. This has advanced the understanding of disease pathogenesis but has not led to widespread changes in care.
J K, Dunbar, H, Campbell
  +8 more sources

Conducting genetic epidemiology research on hyperuricaemia and gout in an indigenous community in Guam - a feasibility study. [PDF]

BMC Public Health
Paulino YC, Camacho F, Paulino TV, Lee DJ, Natividad LL, Matisoo-Smith E, Merriman TR, L Gosling A.   +7 more
europepmc   +3 more sources

Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy. [PDF]

Sci Rep, 2022
Karali M, Testa F, Di Iorio V, Torella A, Zeuli R, Scarpato M, Romano F, Onore ME, Pizzo M, Melillo P, Brunetti-Pierri R, Passerini I, Pelo E, Cremers FPM, Esposito G, Nigro V, Simonelli F, Banfi S.   +17 more
europepmc   +3 more sources

Insights from genomes and genetic epidemiology of SARS-CoV-2 isolates from the state of Andhra Pradesh [PDF]

Epidemiol Infect, 2021
Roja Rani P, Imran M, Lakshmi J, Jolly B, Afsar S, Jain A, Divakar M, Suresh P, Sharma D, Rajesh N, Bhoyar R, Ankaiah D, Shanthi Kumari S, Ranjan G, Anitha Lavanya V, Rophina M, Umadevi S, Sehgal P, Renuka Devi A, Surekha A, Chandra Sekhar P, Hymavathy R, Vanaja P, Scaria V, Sivasubbu S.   +24 more
europepmc   +3 more sources

The PROMOTe study: targeting the gut microbiome with prebiotics to overcome age-related anabolic resistance: protocol for a double-blinded, randomised, placebo-controlled trial

BMC Geriatrics, 2021
Background Loss of skeletal muscle mass and strength occurs with increasing age and is associated with loss of function, disability, and the development of sarcopenia and frailty.
Mary Ni Lochlainn, Ayrun Nessa, Alyce Sheedy, Rachel Horsfall, María Paz García, Deborah Hart, Gulsah Akdag, Darioush Yarand, Samuel Wadge, Andrei-Florin Baleanu, Kevin Whelan, Claire Steves   +11 more
doaj   +1 more source

Overcoming the Negligence in Laboratory Diagnosis of Mucosal Leishmaniasis

Pathogens, 2021
The northern region of Brazil, which has the largest number of cases of tegumentary leishmaniasis (TL) in the country, is also the region that has the highest diversity of species of vectors and Leishmania parasites.
Lilian Motta Cantanhêde, Cristiane Batista Mattos, Ana Karoline Cruz, Yoda Janaina Ikenohuchi, Flavia Gonçalves Fernandes, Enmanuella Helga Ratier Terceiro Medeiros, Cipriano Ferreira da Silva-Júnior, Elisa Cupolillo, Gabriel Eduardo Melim Ferreira, Ricardo de Godoi Mattos Ferreira   +9 more
doaj   +1 more source

Diverging destinies: ‘social’ data within the TwinsUK cohort [version 1; peer review: 2 approved]

Wellcome Open Research, 2022
Background: Twins offer social scientists a unique opportunity to understand the interplay of social factors and physical and mental well-being. TwinsUK is the largest UK registry of adult mono- and dy-zygotic twins, but most of the research that ...
Deborah Hart, Ruth C E Bowyer, Ellen J Thompson, Andrew Anastasiou, Claire J Steves, Jennifer B Dowd, Golboo Abbasian, María Paz García, Genevieve Lachance   +8 more
doaj   +1 more source

GENETIC EPIDEMIOLOGY [PDF]

Annual Review of Genetics, 1993
Every science has roots that antedate acceptance as a discipline. Neglecting these intimations, there is a consensus that population genetics became a recognised science about 1920, and that it split into two branches about 1960. One branch is concerned with historical processes, uniting genetics with anthropology and (in other species) with ...
openaire   +4 more sources

Prenatal diagnosis of Norrie disease after whole exome sequencing of an affected proband during an ongoing pregnancy: a case report

BMC Medical Genetics, 2020
Background Hereditary ophthalmic pathology is a genetically heterogeneous group of diseases that occur either as an isolated eye disorder or as a symptom of hereditary syndromes (chromosomal or monogenic).
Andrey V. Marakhonov, Irina A. Mishina, Vitaly V. Kadyshev, Svetlana A. Repina, Maria F. Shurygina, Olga A. Shchagina, Natalya N. Vasserman, Tatyana A. Vasilyeva, Sergey I. Kutsev, Rena A. Zinchenko   +9 more
doaj   +1 more source