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List of works by Nathan Pankratz

A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

scientific article

A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data

scientific article published on 17 May 2022

A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

scientific article

A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

scientific article published on 05 May 2013

A large-scale exome array analysis of venous thromboembolism

scientific article published on 19 January 2019

A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies

scientific article published on June 2013

A mutation in myotilin causes spheroid body myopathy

scientific article

A plateau in pre-Alzheimer memory decline: evidence for compensatory mechanisms?

scientific article

A two-stage classification approach identifies seven susceptibility genes for a simulated complex disease

scientific article

Alpha-synuclein and familial Parkinson's disease

scientific article

An analysis of measures of effect size by age of onset in cancer genomewide association studies

scientific article published on 14 June 2013

Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities Study

scientific article published on 21 January 2016

Association between mitochondrial DNA copy number and sudden cardiac death: findings from the Atherosclerosis Risk in Communities study (ARIC).

scientific article published on 30 June 2017

Association of Mitochondrial DNA Copy Number With Cardiovascular Disease

scientific article published on 11 October 2017

Chromosome 5 and Parkinson disease

scholarly article by Tatiana Foroud et al published 31 May 2006 in European Journal of Human Genetics

Clinical correlates of depressive symptoms in familial Parkinson's disease

scientific article

Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.

scientific article published on 28 March 2018

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

scientific article

Copy Number Variations and Cognitive Phenotypes in Unselected Populations

scholarly article

Copy number variation in familial Parkinson disease

scientific article

Copy number variations and cognitive phenotypes in unselected populations

scientific article

Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium

scientific article published on 16 October 2017

Discovering genetic interactions bridging pathways in genome-wide association studies

scientific article published on 19 September 2019

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

scientific article published on 24 July 2017

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

scientific article published on 09 March 2022

Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease

scientific article published in June 2004

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

scientific article

Factors related to fungiform papillae density: the beaver dam offspring study

scientific article published on 02 July 2013

Failure to replicate thrombomodulin genetic variant predictors of venous thromboembolism in African Americans

scientific article

Fine Mapping and Identification of BMI Loci in African Americans

scientific article published on October 2013

Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation

scientific article

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

scientific article published on 20 February 2014

Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations

scientific article published on 21 November 2016

Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel loci

scientific article

Genetic and nongenetic risk factors for childhood cancer

scientific article

Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes

scientific article

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

scientific article published in The Lancet

Genetics of Parkinson disease

scientific article

Genetics of Parkinson disease

scientific article published on December 2007

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

scientific article published on 07 June 2002

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease

scientific article

Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE

scientific article

Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

scientific article

Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families

article

Genomewide association study for onset age in Parkinson disease

scientific article

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

scientific article

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease

scientific article

Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study

scientific article

Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

scientific article published on 01 November 2019

Hearing impairment susceptibility in elderly men and the DFNA18 locus

scientific article published in May 2006

Heritability of Vascular Structure and Function: A Parent-Child Study

scientific article published on 2 February 2017

Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

article

Identification of genes for complex disease using longitudinal phenotypes

scientific article

Identifying rare variants from exome scans: the GAW17 experience

scientific article

Inclusion of RBD improves the diagnostic classification of dementia with Lewy bodies

scientific article

Issues in association mapping with high-density SNP data and diverse family structures

scientific article

Joint analyses of disease and correlated quantitative phenotypes using next‐generation sequencing data ⬇️

scientific article published on January 1, 2011

LRRK2 MUTATION ANALYSIS IN PARKINSON DISEASE FAMILIES WITH EVIDENCE OF LINKAGE TO PARK8

article

LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.

scientific article published on 5 September 2007

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

scientific article

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

scientific article

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

scientific article (publication date: September 2014)

Low-Frequency Copy-Number Variants and General Cognitive Ability: No Evidence of Association

scientific article published on January 2014

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

scientific article

Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

scientific article published on 10 May 2019

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

scientific article

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

scientific article

Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study

scientific article

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

scientific article published in 2022

Mutations in DJ-1 are rare in familial Parkinson disease

scientific article

Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset

scientific article

Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease

article

Nearly Half of TP53 Germline Variants Predicted To Be Pathogenic in Patients With Osteosarcoma Are De Novo: A Report From the Children's Oncology Group

scientific article published on 02 October 2020

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

scientific article

Odor identification and cognitive function in the Beaver Dam Offspring Study

scientific article published on 21 June 2013

Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10-Pulmonary Function Association

scientific article published on 01 March 2019

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

scientific article published on July 2009

Parkinson Disease Overview

scientific article published on 25 July 2019

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

scientific article

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia

scientific article published in January 2006

Prevalence of mild cognitive impairment is higher in men. The Mayo Clinic Study of Aging

scientific article

R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation

article

RE: “RACIAL AND ETHNIC DIFFERENCES IN SOCIOECONOMIC POSITION AND RISK OF CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA”

scientific article published on 01 June 2019

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

scientific article

Rare copy number variants identified in prune belly syndrome

scientific article published on 22 November 2017

Rare copy number variants implicated in posterior urethral valves

scientific article published on 14 December 2015

Rare nonsynonymous exonic variants in addiction and behavioral disinhibition

scientific article published on 04 October 2013

Replication of genome-wide association signals in Asian Indians with early-onset type 2 diabetes

scientific article published on 4 August 2016

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

scientific article published on 6 March 2019

Significant linkage of Parkinson disease to chromosome 2q36-37

scientific article

Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease

scientific article published on 12 May 2017

Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease

scientific article published on 30 December 2005

The Familial Intracranial Aneurysm (FIA) study protocol

scientific article

The associations between 6-n-propylthiouracil (PROP) intensity and taste intensities differ by TAS2R38 haplotype

scientific article

The incidence of MCI differs by subtype and is higher in men: the Mayo Clinic Study of Aging

scientific article published on 25 January 2012

Tracking pathophysiological processes in Alzheimer's disease: an updated hypothetical model of dynamic biomarkers ⬇️

scientific article (publication date: February 2013)

Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium

scientific article published on 13 September 2017

Translation initiator EIF4G1 mutations in familial Parkinson disease

scientific article (publication date: 9 September 2011)

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

scientific article published on 23 December 2019

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

scientific article

Validation of a hybrid approach to standardize immunophenotyping analysis in large population studies: The Health and Retirement Study

scientific article published on 29 May 2020

Variants in BAK1, SPRY4, and GAB2 are associated with pediatric germ cell tumors: A report from the children's oncology group.

scientific article published on 13 March 2017

Variation in GIGYF2 is not associated with Parkinson disease

scientific article published on 11 March 2009

Voxel-based morphometry in patients with obsessive-compulsive behaviors in behavioral variant frontotemporal dementia

scientific article

Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects

scientific article

Voxelwise genome-wide association study (vGWAS)

scientific article

Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

scientific article

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

scientific article

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

article

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