Allison Ashley-Koch
Allison Ashley-Koch
Duke University Medical Center
Email verificata su duke.edu
Titolo
Citata da
Citata da
Anno
Sickle Hemoglobin (Hb S) Allele and Sickle Cell Disease: A HuGE Review
A Ashley-Koch, Q Yang, RS Olney
American journal of epidemiology 151 (9), 839-845, 2000
6352000
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)
E Reid, M Kloos, A Ashley-Koch, L Hughes, S Bevan, IK Svenson, ...
The American Journal of Human Genetics 71 (5), 1189-1194, 2002
5582002
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)
E Reid, M Kloos, A Ashley-Koch, L Hughes, S Bevan, IK Svenson, ...
The American Journal of Human Genetics 71 (5), 1189-1194, 2002
5572002
Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism
DQ Ma, PL Whitehead, MM Menold, ER Martin, AE Ashley-Koch, H Mei, ...
The American Journal of Human Genetics 77 (3), 377-388, 2005
3702005
Epidemiologic and genetic aspects of spina bifida and other neural tube defects
KS Au, A Ashley‐Koch, H Northrup
Developmental disabilities research reviews 16 (1), 6-15, 2010
3452010
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ...
Nature genetics 45 (2), 155-163, 2013
2872013
Genomic screen and follow‐up analysis for autistic disorder
Y Shao, CM Wolpert, KL Raiford, MM Menold, SL Donnelly, SA Ravan, ...
American journal of medical genetics 114 (1), 99-105, 2002
2862002
Largest GWAS of PTSD (N= 20 070) yields genetic overlap with schizophrenia and sex differences in heritability
LE Duncan, A Ratanatharathorn, AE Aiello, LM Almli, AB Amstadter, ...
Molecular psychiatry 23 (3), 666-673, 2018
2742018
Identification of MeCP2 mutations in a series of females with autistic disorder
RM Carney, CM Wolpert, SA Ravan, M Shahbazian, A Ashley-Koch, ...
Pediatric neurology 28 (3), 205-211, 2003
2702003
Self-regulation of emotion, functional impairment, and comorbidity among childrenwith AD/HD
AD Anastopoulos, TF Smith, ME Garrett, E Morrissey-Kane, NK Schatz, ...
Journal of attention disorders 15 (7), 583-592, 2011
2642011
Pulmonary hypertension associated with sickle cell disease: clinical and laboratory endpoints and disease outcomes
LM De Castro, JC Jonassaint, FL Graham, A Ashley‐Koch, MJ Telen
American journal of hematology 83 (1), 19-25, 2008
2622008
Relationship between methylome and transcriptome in patients with nonalcoholic fatty liver disease
SK Murphy, H Yang, CA Moylan, H Pang, A Dellinger, MF Abdelmalek, ...
Gastroenterology 145 (5), 1076-1087, 2013
2602013
Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31
S Zchner, G Wang, KN Tran-Viet, MA Nance, PC Gaskell, JM Vance, ...
The American Journal of Human Genetics 79 (2), 365-369, 2006
2502006
Genetic studies of autistic disorder and chromosome 7
A Ashley-Koch, CM Wolpert, MM Menold, L Zaeem, S Basu, SL Donnelly, ...
Genomics 61 (3), 227-236, 1999
2441999
Effects of environmental stress and gender on associations among symptoms of depression and the serotonin transporter gene linked polymorphic region (5-HTTLPR)
BH Brummett, SH Boyle, IC Siegler, CM Kuhn, A Ashley-Koch, ...
Behavior genetics 38 (1), 34-43, 2008
2422008
Factors associated with survival in a contemporary adult sickle cell disease cohort
H Elmariah, ME Garrett, LM De Castro, JC Jonassaint, KI Ataga, ...
American journal of hematology 89 (5), 530-535, 2014
2392014
HLA-DR15 Haplotype and Multiple Sclerosis: A HuGE Review
H Schmidt, D Williamson, A Ashley-Koch
American journal of epidemiology 165 (10), 1097-1109, 2007
2222007
Analysis of the RELN gene as a genetic risk factor for autism
DA Skaar, Y Shao, JL Haines, JE Stenger, J Jaworski, ER Martin, ...
Molecular psychiatry 10 (6), 563-571, 2005
2162005
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
2142021
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder
Y Shao, KL Raiford, CM Wolpert, HA Cope, SA Ravan, AA Ashley-Koch, ...
The American Journal of Human Genetics 70 (4), 1058-1061, 2002
2072002
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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