Các bài viết có thể truy cập công khai - Hakon HakonarsonTìm hiểu thêm
Không có ở bất kỳ nơi nào: 29
Đánh giá
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations
K Bønnelykke, P Sleiman, K Nielsen, E Kreiner-Møller, JM Mercader, ...
Nature genetics 46 (1), 51-55, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health, UK Medical Research Council
Đánh giá
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive …
EM Jackson, AJ Sievert, X Gai, H Hakonarson, AR Judkins, L Tooke, ...
Clinical cancer research 15 (6), 1923-1930, 2009
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Parental ADHD status and its association with proband ADHD subtype and severity
T Takeda, K Stotesbery, T Power, PJ Ambrosini, W Berrettini, ...
The Journal of pediatrics 157 (6), 995-1000. e1, 2010
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Nocturnal enuresis: a suggestive endophenotype marker for a subgroup of inattentive attention-deficit/hyperactivity disorder
J Elia, T Takeda, R Deberardinis, J Burke, J Accardo, PJ Ambrosini, ...
The Journal of pediatrics 155 (2), 239-244. e5, 2009
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Mutations in SCAPER cause autosomal recessive retinitis pigmentosa with intellectual disability
Y Tatour, I Sanchez-Navarro, E Chervinsky, H Hakonarson, H Gawi, ...
Journal of medical genetics 54 (10), 698-704, 2017
Các cơ quan ủy nhiệm: Government of Spain
Đánh giá
A missense mutation in ANKRD26 segregates with thrombocytopenia
SA Al Daama, YH Housawi, W Dridi, M Sager, FG Otieno, C Hou, ...
Blood, The Journal of the American Society of Hematology 122 (3), 461-462, 2013
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Epistasis amongst PTPN2 and genes of the vitamin D pathway contributes to risk of juvenile idiopathic arthritis
JA Ellis, KJ Scurrah, YR Li, AL Ponsonby, RA Chavez, A Pezic, T Dwyer, ...
The Journal of Steroid Biochemistry and Molecular Biology 145, 113-120, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, Australian Research Council, National …
Đánh giá
Recent advances in the genetics and genomics of asthma and related traits
PMA Sleiman, H Hakonarson
Current opinion in pediatrics 22 (3), 307-312, 2010
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
A cis-acting regulatory variant in the IL2RA locus
HQ Qu, DJ Verlaan, B Ge, Y Lu, KCL Lam, R Grabs, E Harmsen, ...
The Journal of Immunology 183 (8), 5158-5162, 2009
Các cơ quan ủy nhiệm: Canadian Institutes of Health Research, Genome Canada
Đánh giá
Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapy
TL Wenger, RA Bly, N Wu, CM Albert, J Park, J Shieh, J Chenbhanich, ...
American journal of medical genetics Part A 182 (7), 1576-1591, 2020
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Etiology of autism spectrum disorder: a genomics perspective
JJ Connolly, H Hakonarson
Current psychiatry reports 16, 1-9, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females
RC Chiaroni-Clarke, YR Li, JE Munro, RA Chavez, KJ Scurrah, A Pezic, ...
Genes & Immunity 16 (7), 495-498, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, Australian Research Council, National …
Đánh giá
Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity
SFA Grant, JT Glessner, JP Bradfield, J Zhao, JE Tirone, RI Berkowitz, ...
International journal of obesity 36 (1), 80-83, 2012
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Analysis of chromosomal structural variation in patients with congenital left‐sided cardiac lesions
PS White, HM Xie, P Werner, J Glessner, B Latney, H Hakonarson, ...
Birth Defects Research Part A: Clinical and Molecular Teratology 100 (12 …, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital …
Y Guo, I Prokudin, C Yu, J Liang, Y Xie, M Flaherty, L Tian, S Crofts, ...
Ophthalmic genetics 36 (4), 333-338, 2015
Các cơ quan ủy nhiệm: National Health and Medical Research Council, Australia
Đánh giá
Attention-deficit hyperactivity disorder and pharmacotherapy—Past, present, and future: A review of the changing landscape of drug therapy
JJ Connolly, JT Glessner, C Kao, J Elia, H Hakonarson
Therapeutic Innovation & Regulatory Science 49 (5), 632-642, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
DENND1B gene variants associate with elevated exhaled nitric oxide in healthy high‐risk neonates
BLK Chawes, AL Bischoff, E Kreiner‐Møller, F Buchvald, H Hakonarson, ...
Pediatric Pulmonology 50 (2), 109-117, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, Danish Council for Independent Research
Đánh giá
CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease
JT Glessner, J Li, A Desai, M Palmer, D Kim, AM Lucas, X Chang, ...
International Journal of Cardiology 298, 107-113, 2020
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Effect of micro-osteoperforations on the gene expression profile of the periodontal ligament of orthodontically moved human teeth
A Spitz, D Adesse, M Gonzalez, R Pellegrino, H Hakonarson, ...
Clinical Oral Investigations, 1-12, 2022
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Morphine dose optimization in critically ill pediatric patients with acute respiratory failure: a population pharmacokinetic-pharmacogenomic study
AF Zuppa, GR Benitez, NR Zane, MAQ Curley, J Bradfield, H Hakonarson, ...
Critical care medicine 47 (6), e485-e494, 2019
Các cơ quan ủy nhiệm: US National Institutes of Health
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