[HTML][HTML] Genetic and nongenetic risk factors for childhood cancer
LG Spector, N Pankratz, EL Marcotte - Pediatric Clinics of North …, 2015 - ncbi.nlm.nih.gov
The causes of childhood cancer have been systematically studied for several decades, but
apart from high-dose radiation and prior chemotherapy there are few or no strong external …
apart from high-dose radiation and prior chemotherapy there are few or no strong external …
[HTML][HTML] Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
The Trans-Omics for Precision Medicine (TOPMed) programme seeks to elucidate the genetic
architecture and biology of heart, lung, blood and sleep disorders, with the ultimate goal of …
architecture and biology of heart, lung, blood and sleep disorders, with the ultimate goal of …
[HTML][HTML] Genetics of Parkinson disease
N Pankratz, T Foroud - Genetics in medicine, 2007 - Elsevier
… These estimates have been derived from mostly North American and Northern European
populations; the G2019S mutation seems to be extremely rare in East Asia. Nevertheless, the …
populations; the G2019S mutation seems to be extremely rare in East Asia. Nevertheless, the …
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
We conducted a meta-analysis of Parkinson's disease genome-wide association studies
using a common set of 7,893,274 variants across 13,708 cases and 95,282 controls. Twenty-six …
using a common set of 7,893,274 variants across 13,708 cases and 95,282 controls. Twenty-six …
[HTML][HTML] Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
More than 800 published genetic association studies have implicated dozens of potential
risk loci in Parkinson's disease (PD). To facilitate the interpretation of these findings, we have …
risk loci in Parkinson's disease (PD). To facilitate the interpretation of these findings, we have …
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
… N Pankratz undertook statistical analyses comparing the clinical phenotype of those with
and without the PARK8 mutation and contributed to the manuscript. D Hernandez undertook …
and without the PARK8 mutation and contributed to the manuscript. D Hernandez undertook …
[PDF][PDF] The polygenic and monogenic basis of blood traits and diseases
…, Y Murakami, GN Nadkarni, K Nikus, N Pankratz… - Cell, 2020 - cell.com
Blood cells play essential roles in human health, underpinning physiological processes
such as immunity, oxygen transport, and clotting, which when perturbed cause a significant …
such as immunity, oxygen transport, and clotting, which when perturbed cause a significant …
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies
…, T Foroud, B Ghetti, WC Nichols, N Pankratz… - JAMA …, 2013 - jamanetwork.com
Importance While mutations in glucocerebrosidase (GBA1) are associated with an increased
risk for Parkinson disease (PD), it is important to establish whether such mutations are also …
risk for Parkinson disease (PD), it is important to establish whether such mutations are also …
[PDF][PDF] Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations
…, M Nauck, K Nikus, WH Ouwehand, N Pankratz… - Cell, 2020 - cell.com
Most loci identified by GWASs have been found in populations of European ancestry (EUR).
In trans-ethnic meta-analyses for 15 hematological traits in 746,667 participants, including …
In trans-ethnic meta-analyses for 15 hematological traits in 746,667 participants, including …
Genomewide association study for susceptibility genes contributing to familial Parkinson disease
… (n = 7,667); (2) there were differential rates of missing genotypes in the cases and controls (n
= 75) or males and females (n … was observed in the control sample (n = 906). Many markers …
= 75) or males and females (n … was observed in the control sample (n = 906). Many markers …