|A cascade of disparities: health and health care access for people with intellectual disabilities|
GL Krahn, L Hammond, A Turner
Mental retardation and developmental disabilities research reviews 12 (1), 70-82, 2006
|Genetics of dementia|
CT Loy, PR Schofield, AM Turner, JBJ Kwok
The Lancet 383 (9919), 828-840, 2014
|Understanding the information needs of public health practitioners: a literature review to inform design of an interactive digital knowledge management system|
D Revere, AM Turner, A Madhavan, N Rambo, PF Bugni, AM Kimball, ...
Journal of biomedical informatics 40 (4), 410-421, 2007
|The use of social networking sites for public health practice and research: a systematic review|
D Capurro, K Cole, MI Echavarrķa, J Joe, T Neogi, AM Turner
Journal of medical Internet research 16 (3), e79, 2014
|Nonhematopoietic tumor cell lines express stem cell factor and display c-kit receptors|
AM Turner, KM Zsebo, F Martin, FW Jacobsen, LG Bennett, VC Broudy
|FLT3 receptor expression on the surface of normal and malignant human hematopoietic cells|
AM Turner, NL Lin, S Issarachai, SD Lyman, VC Broudy
|Prediction of late death or disability at age 5 years using a count of 3 neonatal morbidities in very low birth weight infants|
B Schmidt, RS Roberts, PG Davis, LW Doyle, EV Asztalos, G Opie, ...
The Journal of pediatrics 167 (5), 982-986. e2, 2015
|Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity|
G Chenevix-Trench, C Wicking, J Berkman, H Sharpe, A Hockey, E Haan, ...
American journal of human genetics 53 (3), 760, 1993
|Germline loss-of-function mutations in EPHB4 cause a second form of capillary malformation-arteriovenous malformation (CM-AVM2) deregulating RAS-MAPK signaling|
M Amyere, N Revencu, R Helaers, E Pairet, E Baselga, M Cordisco, ...
Circulation 136 (11), 1037-1048, 2017
|Incontinentia pigmenti case series: clinical spectrum of incontinentia pigmenti in 53 female patients and their relatives|
TA Phan, O Wargon, AM Turner
Clinical and Experimental Dermatology: Clinical dermatology 30 (5), 474-480, 2005
|Identification and characterization of a soluble c-kit receptor produced by human hematopoietic cell lines|
AM Turner, LG Bennett, NL Lin, J Wypych, TD Bartley, RW Hunt, HL Atkins, ...
|Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disorders|
LJ Ewans, D Schofield, R Shrestha, Y Zhu, V Gayevskiy, K Ying, C Walsh, ...
Genetics in Medicine 20 (12), 1564-1574, 2018
|ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism|
R Desai, AE Frazier, R Durigon, H Patel, AW Jones, I Dalla Rosa, NJ Lake, ...
Brain 140 (6), 1595-1610, 2017
|Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficiencies|
B Ilkovski, AT Pagnamenta, GL O'Grady, T Kinoshita, MF Howard, M Lek, ...
Human molecular genetics 24 (21), 6146-6159, 2015
|Scenario-based design: A method for connecting information system design with public health operations and emergency management|
B Reeder, AM Turner
Journal of biomedical informatics 44 (6), 978-988, 2011
|Differential expression of pyloric atresia in junctional epidermolysis bullosa with ITGB4 mutations suggests that pyloric atresia is due to factors other than the mutations and …|
N Dang, S Klingberg, AI Rubin, M Edwards, S Borelli, J Relic, P Marr, ...
Acta dermato-venereologica 88 (5), 438-448, 2008
|Modeling public health interventions for improved access to the gray literature|
AM Turner, ED Liddy, J Bradley, JA Wheatley
Journal of the Medical Library Association 93 (4), 487, 2005
|Using crowdsourcing technology for testing multilingual public health promotion materials|
AM Turner, K Kirchhoff, D Capurro
Journal of medical Internet research 14 (3), e79, 2012
|Application of statistical machine translation to public health information: a feasibility study|
K Kirchhoff, AM Turner, A Axelrod, F Saavedra
Journal of the American Medical Informatics Association 18 (4), 473-478, 2011
|Cantu syndrome: report of nine new cases and expansion of the clinical phenotype|
I Scurr, L Wilson, M Lees, S Robertson, E Kirk, A Turner, J Morton, A Kidd, ...
American journal of medical genetics Part A 155 (3), 508-518, 2011