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1.
Drug-resistant epilepsy classified by a phenotyping algorithm associates with NTRK2.
Acta Neurol Scand
; 140(3): 169-176, 2019 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-31070779
2.
Leveraging electronic health records to assess the role of ADRB2 single nucleotide polymorphisms in predicting exacerbation frequency in asthma patients.
Pharmacogenet Genomics
; 28(11): 256-259, 2018 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-30334910
3.
Identification of Four Novel Loci in Asthma in European American and African American Populations.
Am J Respir Crit Care Med
; 195(4): 456-463, 2017 Feb 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-27611488
4.
Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic association studies.
BMC Infect Dis
; 16(1): 684, 2016 11 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-27855652
5.
Novel locus for atopic dermatitis in African Americans and replication in European Americans.
J Allergy Clin Immunol
; 143(3): 1229-1231, 2019 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-30414857
6.
Mendelian randomization analysis demonstrates that low vitamin D is unlikely causative for pediatric asthma.
J Allergy Clin Immunol
; 138(6): 1747-1749.e4, 2016 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-27554823
7.
Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder.
PLoS One
; 11(7): e0159621, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27472449
8.
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital Amaurosis.
Ophthalmic Genet
; 36(4): 333-8, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-24547928
9.
Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes.
Front Genet
; 5: 96, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24860591
10.
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism.
Nat Commun
; 5: 4074, 2014 Jun 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-24927284
11.
AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate.
JIMD Rep
; 14: 77-85, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24515575
12.
Erratum to: AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate.
JIMD Rep
; 14: 119, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24973975
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