Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Megan Priston"'
Autor:
Tianhua Huang, PhD, Shamim Rashid, BSc, Megan Priston, MS, Evasha Rasasakaram, MS, Ellen Mak-Tam, BSc, Clare Gibbons, MS, Elad Mei-Dan, MD, H. Melanie Bedford, MD
Publikováno v:
AJOG Global Reports, Vol 3, Iss 2, Pp 100193- (2023)
BACKGROUND: Professional societies have recommended universal first trimester screening for preeclampsia and a second or third trimester soluble fms-like tyrosine kinase-1–placental growth factor ratio test to assess for preeclampsia and its severi
Externí odkaz:
https://doaj.org/article/9254205448d64ea9ab6b868716ca4292
Autor:
Tianhua Huang, H. Melanie Bedford, Shamim Rashid, Evasha Rasasakaram, Megan Priston, Ellen Mak-Tam, Clare Gibbons, Wendy S. Meschino, Howard Cuckle, Elad Mei-Dan
Publikováno v:
BMC Pregnancy and Childbirth, Vol 22, Iss 1, Pp 1-14 (2022)
Abstract Background Abnormal levels of maternal biochemical markers used in multiple marker aneuploidy screening have been associated with adverse pregnancy outcomes. This study aims to assess if a combination of maternal characteristics and biochemi
Externí odkaz:
https://doaj.org/article/6296fe0375c74458a6a421fe71e136cc
Autor:
Tianhua Huang, Shamim Rashid, Alan Dennis, Ellen Mak-Tam, Megan Priston, Clare Gibbons, Melanie Bedford, Wendy Meschino, Howard Cuckle, Elad Mei-Dan
Publikováno v:
American Journal of Obstetrics and Gynecology. 226:S638
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cbe4a969c638f969b4460d4e5a25881
https://doi.org/10.1016/j.ajog.2021.11.1053
https://doi.org/10.1016/j.ajog.2021.11.1053
Autor:
Tianhua Huang, Shamim Rashid, Ellen Mak-Tam, Megan Priston, Clare Gibbons, Melanie Bedford, Elad Mei-Dan
Publikováno v:
American Journal of Obstetrics and Gynecology. 226:S338
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d551ecfd39aabedea3d17afe56947273
https://doi.org/10.1016/j.ajog.2021.11.566
https://doi.org/10.1016/j.ajog.2021.11.566
Publikováno v:
Journal of Medical Genetics. 37:422-427
Glaucoma is a leading cause of irreversible blindness in Canada. Congenital glaucoma usually manifests during the first years of life and is characterised by severe visual loss and autosomal recessive inheritance. Two disease loci, on chromosomes 1p3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e78fe3fdd5ac41893bcc6149e86adff3
https://doi.org/10.1136/jmg.37.6.422
https://doi.org/10.1136/jmg.37.6.422
Autor:
Elise Héon, Philippe Othenin Girard, Gail Billingsley, Nicolette H. Lubsen, Daniel F. Schorderet, Megan Priston, Francis L. Munier
Publikováno v:
The American Journal of Human Genetics. 65:1261-1267
Despite the fact that cataracts constitute the leading cause of blindness worldwide, the mechanisms of lens opacification remain unclear. We recently mapped the aculeiform cataract to the gamma-crystallin locus (CRYG) on chromosome 2q33-35, and mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a786536164f43a3b328e38b28abe1c6
https://doi.org/10.1086/302619
https://doi.org/10.1086/302619
Autor:
Andrea, Vincent, Gail, Billingsley, Megan, Priston, Tom, Glaser, Edward, Oliver, Mike, Walter, Robert, Ritch, Alex, Levin, Elise, Heon
Publikováno v:
Molecular vision. 12
Peters anomaly is a developmental anomaly of the eye frequently associated with glaucoma. The aim of this study was to further define the molecular basis of this condition.The role of four candidate genes implicated in ocular development or glaucoma,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d02092dd5603d656b6a2ffe24b562b44
https://pubmed.ncbi.nlm.nih.gov/16735991
https://pubmed.ncbi.nlm.nih.gov/16735991
Autor:
Colin E, Willoughby, Ayad, Shafiq, Walter, Ferrini, Louie Loh Yen, Chan, Gail, Billingsley, Megan, Priston, Calvin, Mok, Arvind, Chandna, Stephen, Kaye, Elise, Héon
Publikováno v:
Molecular vision. 11
The molecular characterization of a UK family with an autosomal dominant congenital cataract associated with microcornea is reported.Family history and clinical data were recorded. This phenotype was linked to a 7.6 cM region of chromosome 22q11.2-q1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::55b22cd1838a3cc4a0af2855c700ca65
https://pubmed.ncbi.nlm.nih.gov/16110300
https://pubmed.ncbi.nlm.nih.gov/16110300
Autor:
Yvonne M. Buys, Elise Heon, Gail Billingsley, Graham E. Trope, Donna Williams-Lyn, Megan Priston, Alex V. Levin, Andrea L Vincent
Publikováno v:
American journal of human genetics. 70(2)
“Early-onset glaucoma” refers to genetically heterogeneous conditions for which glaucoma manifests at age 5–40 years and for which only a small subset is molecularly characterized. We studied the role of MYOC, CYP1B1, and PITX2 in a population
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3470aa4947c7446ed9eec2e8ea1e0e4c
https://pubmed.ncbi.nlm.nih.gov/11774072
https://pubmed.ncbi.nlm.nih.gov/11774072
Autor:
Andrea L Vincent, Thomas M Glaser, Donna Williams-Lyn, Alex V. Levin, Megan Priston, Elise Héon, Edward R. Oliver, Godfrey Heathcote, Michael A. Walter, Gail Billingsley, Joanne Sutherland
Congenital glaucoma refers to a genetically heterogeneous group of distinctive clinical diseases characterised by increased intraocular pressure most often associated with increased corneal diameter, corneal oedema, and consequent visual impairment.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06fcdb21cc80a602f5483d89714304cd
https://europepmc.org/articles/PMC1734880/
https://europepmc.org/articles/PMC1734880/
