Author

Albert E Chudley

Professor Emeritus, Paediatrics and Child Health, University of Manitoba - Cited by 13,906 - genetics - birth defects - Fetal alcohol spectrum disorder

Biography

Albert Chudley studied in the Departments of Pediatrics and Child Health and Biochemistry and Medical Genetics, Max Rady College of Medicine; University of Manitoba, Winnipeg, Canada. Dr. Chudley is highly rated in 9 conditions, His top areas of expertise are Fetal Alcohol Syndrome, Bifid Nose, Developmental Expressive Language Disorder, and Grix Blankenship Peterson Syndrome.
Title
Cited by
Year
Fetal alcohol spectrum disorder: a guideline for diagnosis across the lifespan
JL Cook, CR Green, CM Lilley, SM Anderson, ME Baldwin, AE Chudley, ...Cmaj 188 (3), 191-197, 2016201
553
2016
Comorbidity of fetal alcohol spectrum disorder: a systematic review and meta-analysis
S Popova, S Lange, K Shield, A Mihic, AE Chudley, RAS Mukherjee, ...The Lancet 387 (10022), 978-987, 2016201
523
2016
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
G Wheway, M Schmidts, DA Mans, K Szymanska, TMT Nguyen, H Racher, ...Nature cell biology 17 (8), 1074-1087, 2015201
231
2015
Autosomal-recessive intellectual disability with cerebellar atrophy syndrome caused by mutation of the manganese and zinc transporter gene SLC39A8
KM Boycott, CL Beaulieu, KD Kernohan, OH Gebril, A Mhanni, ...The American Journal of Human Genetics 97 (6), 886-893, 2015201
182
2015
Kabuki syndrome: international consensus diagnostic criteria
MP Adam, S Banka, HT Bjornsson, O Bodamer, AE Chudley, J Harris, ...Journal of medical genetics 56 (2), 89-95, 2019201
150
2019
DNA methylation signature of human fetal alcohol spectrum disorder
E Portales-Casamar, AA Lussier, MJ Jones, JL MacIsaac, RD Edgar, ...Epigenetics & chromatin 9 (1), 1-20, 2016201
145
2016
CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease
KA Strauss, RN Jinks, EG Puffenberger, S Venkatesh, K Singh, I Cheng, ...The American Journal of Human Genetics 96 (1), 121-135, 2015201
136
2015
Population-based prevalence of fetal alcohol spectrum disorder in Canada
S Popova, S Lange, V Poznyak, AE Chudley, KD Shield, JN Reynolds, ...BMC public health 19 (1), 1-12, 2019201
86
2019
Factors influencing ovulation and the risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
J Kotsopoulos, J Lubinski, J Gronwald, C Cybulski, R Demsky, ...International journal of cancer 137 (5), 1136-1146, 2015201
81
2015
DNA methylation as a predictor of fetal alcohol spectrum disorder
AA Lussier, AM Morin, JL MacIsaac, J Salmon, J Weinberg, JN Reynolds, ...Clinical epigenetics 10 (1), 1-14, 2018201
80
2018
It’sa shame! Stigma against fetal alcohol spectrum disorder: Examining the ethical implications for public health practices and policies
E Bell, G Andrew, N Di Pietro, AE Chudley, J N. Reynolds, E RacinePublic Health Ethics 9 (1), 65-77, 2016201
76
2016
Human brain abnormalities associated with prenatal alcohol exposure and fetal alcohol spectrum disorder
JS Jarmasz, DA Basalah, AE Chudley, MR Del BigioJournal of Neuropathology & Experimental Neurology 76 (9), 813-833, 2017201
69
2017
World Health organization International study on the prevalence of fetal alcohol spectrum disorder (FASD)
S Popova, S Lange, AE Chudley, JN Reynolds, J Rehm, PA May, ...Canadian Component, Centre for Addiction and Mental Health, 2018201
65
2018
Relationships between head circumference, brain volume and cognition in children with prenatal alcohol exposure
S Treit, D Zhou, AE Chudley, G Andrew, C Rasmussen, SM Nikkel, ...PloS one 11 (2), e0150370, 2016201
62
2016
Overview of the genetic basis and epigenetic mechanisms that contribute to FASD pathobiology.
VR Liyanage, K Curtis, RM Zachariah, AE Chudley, M RastegarCurrent topics in medicinal chemistry 17 (7), 808-828, 2017201
48
2017
Treatment of infertility does not increase the risk of ovarian cancer among women with a BRCA1 or BRCA2 mutation
J Gronwald, K Glass, B Rosen, B Karlan, N Tung, SL Neuhausen, ...Fertility and sterility 105 (3), 781-785, 2016201
47
2016
A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype
L Li, N Hamel, K Baker, MJ McGuffin, M Couillard, A Gologan, VA Marcus, ...Journal of medical genetics 52 (5), 348-352, 2015201
40
2015
The association between smoking and cancer incidence in BRCA1 and BRCA2 mutation carriers
KP Ko, SJ Kim, T Huzarski, J Gronwald, J Lubinski, HT Lynch, S Armel, ...International journal of cancer 142 (11), 2263-2272, 2018201
30
2018
The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study
J Iqbal, A Nussenzweig, J Lubinski, T Byrski, A Eisen, L Bordeleau, ...British journal of cancer 114 (10), 1160-1164, 2016201
29
2016
Visual search for feature conjunctions: an fMRI study comparing alcohol-related neurodevelopmental disorder (ARND) to ADHD
CR O’Conaill, KL Malisza, JL Buss, RB Bolster, C Clancy, PD de Gervai, ...Journal of neurodevelopmental disorders 7, 1-18, 2015201
29
2015

Referred From: https://scholar.google.com/citations?user=JjrJ6tkAAAAJ&hl=en

Cited by
Citations 13906
h-index 61
i10-index 174
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