User profiles for Hakon Hakonarson
Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENN Verified email at email.chop.edu Cited by 152684 |
[HTML][HTML] Rare variants create synthetic genome-wide associations
Genome-wide association studies (GWAS) have now identified at least 2,000 common
variants that appear associated with common diseases or related traits ( http://www.genome.gov/…
variants that appear associated with common diseases or related traits ( http://www.genome.gov/…
Distinct features of SARS-CoV-2-specific IgA response in COVID-19 patients
…, F Ye, L Guan, D Hu, H Hakonarson… - European …, 2020 - Eur Respiratory Soc
In comparison to severe acute respiratory syndrome coronavirus (SARS-CoV), SARS-CoV-2
appears to be more contagious [1], and coronavirus disease 2019 (COVID-19) patients …
appears to be more contagious [1], and coronavirus disease 2019 (COVID-19) patients …
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes
…, D Beekly, LA Cupples, H Hakonarson… - Archives of …, 2010 - jamanetwork.com
Objectives: To determine whether genotypes at CLU, PICALM, and CR1 confer risk for
Alzheimer disease (AD) and whether risk for AD associated with these genes is influenced by …
Alzheimer disease (AD) and whether risk for AD associated with these genes is influenced by …
[PDF][PDF] Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease
Previous genome-wide association (GWA) studies typically focus on single-locus analysis,
which may not have the power to detect the majority of genuinely associated loci. Here, we …
which may not have the power to detect the majority of genuinely associated loci. Here, we …
[HTML][HTML] Chromosome 6p22 locus associated with clinically aggressive neuroblastoma
Background Neuroblastoma is a malignant condition of the developing sympathetic nervous
system that most commonly affects young children and is often lethal. Its cause is not known…
system that most commonly affects young children and is often lethal. Its cause is not known…
Integrative genomics identifies LMO1 as a neuroblastoma oncogene
Neuroblastoma is a childhood cancer of the sympathetic nervous system that accounts for
approximately 10% of all paediatric oncology deaths 1 , 2 . To identify genetic risk factors for …
approximately 10% of all paediatric oncology deaths 1 , 2 . To identify genetic risk factors for …
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma
…, J Jagannathan, V Latorre, A Iolascon, H Hakonarson… - Nature …, 2012 - nature.com
Neuroblastoma is a cancer of the sympathetic nervous system that accounts for approximately
10% of all pediatric oncology deaths 1 . Here, we report a genome-wide association study …
10% of all pediatric oncology deaths 1 . Here, we report a genome-wide association study …
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
High-throughput sequencing platforms are generating massive amounts of genetic variation
data for diverse genomes, but it remains a challenge to pinpoint a small subset of …
data for diverse genomes, but it remains a challenge to pinpoint a small subset of …
Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
…, MS Silverberg, V Annese, H Hakonarson… - Nature, 2012 - nature.com
Crohn’s disease and ulcerative colitis, the two common forms of inflammatory bowel disease
(IBD), affect over 2.5 million people of European ancestry, with rising prevalence in other …
(IBD), affect over 2.5 million people of European ancestry, with rising prevalence in other …
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
…, JR Gilbert, M Mayhaus, L Lannfelt, H Hakonarson… - Nature …, 2013 - nature.com
Eleven susceptibility loci for late-onset Alzheimer's disease (LOAD) were identified by previous
studies; however, a large portion of the genetic risk for this disease remains unexplained. …
studies; however, a large portion of the genetic risk for this disease remains unexplained. …