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List of works by Allison Ashley-Koch

5-HTTLPR and gender moderate changes in negative affect responses to tryptophan infusion

scientific article published on 26 July 2008

A blood spot method for detecting fumonisin-induced changes in putative sphingolipid biomarkers in LM/Bc mice and humans

scientific article

A common variant near TGFBR3 is associated with primary open angle glaucoma.

scientific article published on 10 April 2015

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia

scientific article

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

scientific article

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

scientific article

A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12

A preliminary analysis of interactions between genotype, retrospective ADHD symptoms, and initial reactions to smoking in a sample of young adults

scientific article published on 20 July 2011

A second leaky splice-site mutation in the spastin gene

scientific article

AGTR1 gene variation: association with depression and frontotemporal morphology

scientific article

APOE ε4 associated with preserved executive function performance and maintenance of temporal and cingulate brain volumes in younger adults

scientific article published on 3 February 2016

Adverse subpopulation regression for multivariate outcomes with high-dimensional predictors

scientific article published on 24 July 2012

Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample

scientific article (publication date: 26 January 2017)

Alloimmunization in sickle cell disease: changing antibody specificities and association with chronic pain and decreased survival

scientific article published on December 2014

An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder

scientific article published in May 2006

An autosomal genomic screen for dementia in an extended Amish family

scientific article published in May 2005

An examination of the association between 5-HTTLPR, combat exposure, and PTSD diagnosis among U.S. veterans

scientific article

Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes

scientific article published in December 2004

Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity

scientific article published on 25 October 2014

Angiotensin receptor gene polymorphisms and 2-year change in hyperintense lesion volume in men.

scientific article

Association analysis of the COMT/MTHFR genes and geriatric depression: an MRI study of the putamen

scientific article published on August 2009

Association between the oxytocin receptor (OXTR) gene and mesolimbic responses to rewards

scientific article published on 31 January 2014

Association of Genetic Variants with Primary Open-Angle Glaucoma among Individuals with African Ancestry

scientific article published on 01 November 2019

Association of gene variants of the renin-angiotensin system with accelerated hippocampal volume loss and cognitive decline in old age

scientific article

Associations of a regulatory polymorphism of monoamine oxidase-A gene promoter (MAOA-uVNTR) with symptoms of depression and sleep quality

scientific article published on June 2007

BDNF Val66Met genotype and 6-month remission rates in late-life depression

scientific article

Bipolar disorder, brain-derived neurotrophic factor (BDNF) Val66Met polymorphism and brain morphology

scientific article

Cadmium exposure and the epigenome: Exposure-associated patterns of DNA methylation in leukocytes from mother-baby pairs.

scientific article published on 28 October 2013

Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation

scientific article published on 20 May 2021

Central nervous system serotonin and clustering of hostility, psychosocial, metabolic, and cardiovascular endophenotypes in men.

scientific article published on July 2010

Childhood socioeconomic status and serotonin transporter gene polymorphism enhance cardiovascular reactivity to mental stress

scientific article published on 24 December 2007

Clinical and metabolomic risk factors associated with rapid renal function decline in sickle cell disease

scientific article published on 27 September 2018

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.

scientific article published on April 2012

DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma

scientific article

Design, methodological issues and participation in a multiple sclerosis case-control study

scientific article published on 16 December 2011

Determining Genetic Component of a Disease

Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma

scientific article

Duffy (Fy), DARC, and neutropenia among women from the United States, Europe and the Caribbean

scientific article published on 4 February 2009

EFFECT OF THE APOE ε4 ALLELE AND COMBAT EXPOSURE ON PTSD AMONG IRAQ/AFGHANISTAN-ERA VETERANS

scientific article

Effect of genetic variation in the nicotinic receptor genes on risk for posttraumatic stress disorder

scientific article

Effects of 5HTTLPR on cardiovascular response to an emotional stressor

scientific article

Effects of environmental stress and gender on associations among symptoms of depression and the serotonin transporter gene linked polymorphic region (5-HTTLPR).

scientific article published on 23 October 2007

Effects of postnatal parental smoking on parent and teacher ratings of ADHD and oppositional symptoms

scientific article published on June 2009

Epidemiologic and genetic aspects of spina bifida and other neural tube defects

scientific article

Epigenome-wide association of PTSD from heterogeneous cohorts with a common multi-site analysis pipeline

journal article published in 2017

Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR

scientific article published on 24 November 2020

Evidence for fumonisin inhibition of ceramide synthase in humans consuming maize-based foods and living in high exposure communities in Guatemala

scientific article published on 12 August 2015

Examination of factors associated with instability of the FMR1 CGG repeat.

scientific article

Exome analysis of two limb-girdle muscular dystrophy families: mutations identified and challenges encountered

scientific article

Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data

scientific article

Factors associated with survival in a contemporary adult sickle cell disease cohort

scientific article published on 21 February 2014

Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster

scientific article

Fiber tract-specific white matter lesion severity Findings in late-life depression and by AGTR1 A1166C genotype

scientific article published on 22 October 2011

Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia

article

Folate metabolism genes, dietary folate and response to antidepressant medications in late-life depression

scientific article published on 20 December 2012

Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects

scientific article

Further evidence for a role of the ADRB2 gene in risk for posttraumatic stress disorder

scientific article published on 17 September 2016

Gene expression profile in human trabecular meshwork from patients with primary open-angle glaucoma

scientific article published on 27 September 2013

Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients

scientific article published on 29 May 2013

Generalized admixture mapping for complex traits

scientific article published on 08 July 2013

Genes implicated in serotonergic and dopaminergic functioning predict BMI categories

scientific article

Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype

scientific article

Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis

scientific article published on 30 August 2017

Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation

scientific article

Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study

scientific article

Genetic polymorphisms associated with priapism in sickle cell disease

scientific article published on 01 May 2007

Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus

scientific article

Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families

scientific article

Genetics of the Chiari I and II Malformations

article

Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia

scientific article

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

scientific article published on 06 January 2013

Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma

scientific article published on 11 January 2016

Genome-wide association study and meta-analysis of intraocular pressure

scientific article published on 04 September 2013

Genome-wide association study of posttraumatic stress disorder in a cohort of Iraq-Afghanistan era veterans

scientific article

Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma.

scientific article

Genomic screen and follow-up analysis for autistic disorder

scientific article published in January 2002

HLA-DR15 haplotype and multiple sclerosis: a HuGE review

scientific article

HPA axis function in male caregivers: effect of the monoamine oxidase-A gene promoter (MAOA-uVNTR).

scientific article published on July 2008

Heavy metals, organic solvents, and multiple sclerosis: An exploratory look at gene-environment interactions

scientific article

Hepatic gene expression profiles differentiate presymptomatic patients with mild versus severe nonalcoholic fatty liver disease.

scientific article published on 13 December 2013

IL28B rs12979860 is not associated with histologic features of NAFLD in a cohort of Caucasian North American patients.

scientific article published on 11 October 2012

Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia

scientific article

Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics

scientific article

Identification of MeCP2 mutations in a series of females with autistic disorder

scientific article (publication date: March 2003)

Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease

scientific article

Impact of BDNF Val66Met and 5-HTTLPR polymorphism variants on neural substrates related to sadness and executive function.

scientific article published on 28 January 2012

Impact of psychological stress on the associations between apolipoprotein E variants and metabolic traits: findings in an American sample of caregivers and controls

scientific article published on 13 May 2010

In vivo Modeling Implicates APOL1 in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress

scientific article

Influence of the MTHFR C677T polymorphism on magnetic resonance imaging hyperintensity volume and cognition in geriatric depression

scientific article

Interactions between genotype and depressive symptoms on obesity

scientific article

Interactions between genotype and retrospective ADHD symptoms predict lifetime smoking risk in a sample of young adults

scientific article

International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

scientific article published on 08 October 2019

Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations

scientific article published on 10 July 2004

Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry

scientific article published on 17 September 2013

Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk

scientific article published in August 2007

Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation. ⬇️

scientific article

Lack of Duffy antigen expression is associated with organ damage in patients with sickle cell disease

scientific article

Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability.

scientific article published on 25 April 2017

Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

article published in 2018

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing

scientific article published on 26 July 2005

Linkage of familial essential tremor to chromosome 5q35.

scientific article

Linkage to a known gene but no mutation identified: comprehensive reanalysis ofSPG4 HSP pedigrees reveals large deletions as the sole cause

article

MYH9 and APOL1 are both associated with sickle cell disease nephropathy

scientific article published on 13 September 2011

Maternal vitamin D receptor genetic variation contributes to infant birthweight among black mothers.

scientific article published on 5 May 2011

Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans

scientific article published on August 2012

Missing genetic risk in neural tube defects: can exome sequencing yield an insight?

scientific article

Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31

scientific article

Natural food folate and late-life depression

scientific article published in October 2009

Negative life stress and longitudinal hippocampal volume changes in older adults with and without depression

scientific article published on 8 March 2013

Nicotinic receptor gene variants interact with attention deficient hyperactive disorder symptoms to predict smoking trajectories from early adolescence to adulthood

scientific article published on July 2013

No association between RORA polymorphisms and PTSD in two independent samples

scientific article published on 22 July 2014

No association between the WNT2 gene and autistic disorder

scientific article published in January 2002

Outcome and life satisfaction of adults with myelomeningocele

scientific article published on 10 January 2013

PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia

scientific article published on 19 November 2020

Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease

scientific article

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder

scientific article published on March 2002

Pregnancy continuation and organizational religious activity following prenatal diagnosis of a lethal fetal defect are associated with improved psychological outcome

scientific article published on 26 May 2015

Pulmonary hypertension associated with sickle cell disease: Clinical and laboratory endpoints and disease outcomes

Refinement of 2q and 7p loci in a large multiplex NTD family

article

Relationship between methylome and transcriptome in patients with nonalcoholic fatty liver disease

scientific article published on 31 July 2013

Risk of meningomyelocele mediated by the common 22q11.2 deletion

scientific article published on 02 May 2024

SLITRK1 mutations in trichotillomania

scientific article

Self-Regulation of Emotion, Functional Impairment, and Comorbidity Among ChildrenWith AD/HD.

scientific article

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

scientific article published on 6 March 2019

Sleep quality varies as a function of 5-HTTLPR genotype and stress

scientific article published on 31 August 2007

Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathy

scientific article

Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.

scientific article

Surgical and obstetric outcomes in adults with sickle cell disease

scientific article published on October 2008

TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone.

scientific article

Testing for contributions of mitochondrial DNA mutations to complex diseases

scientific article published in 1998

Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets

scientific article published in February 2018

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects

scientific article

The PsychENCODE project

scientific article

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

scientific article

The kinetics of urinary fumonisin B1 excretion in humans consuming maize-based diets

scientific article published on 20 July 2012

The serotonin transporter gene polymorphism (5HTTLPR) moderates the effect of adolescent environmental conditions on self-esteem in young adulthood: a structural equation modeling approach

scientific article published on June 2012

Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE).

scientific article

Traumatic stress and accelerated DNA methylation age: A meta-analysis.

scientific article published on 27 December 2017

Urinary fumonisin B1 and estimated fumonisin intake in women from high- and low-exposure communities in Guatemala

scientific article

beta(2)-Adrenergic receptor and adenylate cyclase gene polymorphisms affect sickle red cell adhesion

scientific article published in April 2008

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