Erin Heinzen
Erin Heinzen
Associate Professor, UNC Eshelman School of Pharmacy
Geverifieerd e-mailadres voor unc.edu
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Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance
D Ge, J Fellay, AJ Thompson, JS Simon, KV Shianna, TJ Urban, ...
Nature 461 (7262), 399-401, 2009
40482009
HLA-A* 3101 and carbamazepine-induced hypersensitivity reactions in Europeans
M McCormack, A Alfirevic, S Bourgeois, JJ Farrell, D Kasperavičiūtė, ...
New England Journal of Medicine 364 (12), 1134-1143, 2011
8242011
De novo mutations in epileptic encephalopathies
AS Allen, SF Berkovic, P Cossette, N Delanty, D Dlugos, EE Eichler, ...
Nature 501 (7466), 217-221, 2013
7082013
Genic intolerance to functional variation and the interpretation of personal genomes
S Petrovski, Q Wang, EL Heinzen, AS Allen, DB Goldstein
PLoS genetics 9 (8), 2013
6782013
A genome-wide investigation of SNPs and CNVs in schizophrenia
AC Need, D Ge, ME Weale, J Maia, S Feng, EL Heinzen, KV Shianna, ...
PLoS genetics 5 (2), 2009
4912009
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), eaap8757, 2018
4362018
De novo mutations in epileptic encephalopathies
KC Epi, PE Phenome, AS Allen, SF Berkovic, P Cossette, N Delanty, ...
Nature 501 (7466), 217-221, 2013
3952013
Somatic activation of AKT3 causes hemispheric developmental brain malformations
A Poduri, GD Evrony, X Cai, PC Elhosary, R Beroukhim, MK Lehtinen, ...
Neuron 74 (1), 41-48, 2012
3302012
Tissue-specific genetic control of splicing: implications for the study of complex traits
EL Heinzen, D Ge, KD Cronin, JM Maia, KV Shianna, WN Gabriel, ...
PLoS biology 6 (12), 2008
2972008
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
EL Heinzen, KJ Swoboda, Y Hitomi, F Gurrieri, S Nicole, B de Vries, ...
Nature genetics 44 (9), 1030-1034, 2012
2842012
Rare deletions at 16p13. 11 predispose to a diverse spectrum of sporadic epilepsy syndromes
EL Heinzen, RA Radtke, TJ Urban, GL Cavalleri, C Depondt, AC Need, ...
The American Journal of Human Genetics 86 (5), 707-718, 2010
2432010
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
The American Journal of Human Genetics 95 (4), 360-370, 2014
2002014
The characterization of twenty sequenced human genomes
K Pelak, KV Shianna, D Ge, JM Maia, M Zhu, JP Smith, ET Cirulli, J Fellay, ...
PLoS genetics 6 (9), 2010
1762010
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome
MC Manzini, DE Tambunan, RS Hill, WY Tim, TM Maynard, EL Heinzen, ...
The American Journal of Human Genetics 91 (3), 541-547, 2012
1622012
Genome-wide mRNA expression correlates of viral control in CD4+ T-cells from HIV-1-infected individuals
M Rotger, KK Dang, J Fellay, EL Heinzen, S Feng, P Descombes, ...
PLoS pathogens 6 (2), 2010
1532010
Distinct neurological disorders with ATP1A3 mutations
EL Heinzen, A Arzimanoglou, A Brashear, SJ Clapcote, F Gurrieri, ...
The Lancet Neurology 13 (5), 503-514, 2014
1522014
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
D Kasperavičiūtė, CB Catarino, EL Heinzen, C Depondt, GL Cavalleri, ...
Brain 133 (7), 2136-2147, 2010
1492010
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB
AC Need, DK Attix, JM McEvoy, ET Cirulli, KL Linney, P Hunt, D Ge, ...
Human molecular genetics 18 (23), 4650-4661, 2009
1492009
Screening the human exome: a comparison of whole genome and whole transcriptome sequencing
ET Cirulli, A Singh, KV Shianna, D Ge, JP Smith, JM Maia, EL Heinzen, ...
Genome biology 11 (5), R57, 2010
1332010
Genome-wide scan of copy number variation in late-onset Alzheimer's disease
EL Heinzen, AC Need, KM Hayden, O Chiba-Falek, AD Roses, ...
Journal of Alzheimer's Disease 19 (1), 69-77, 2010
1212010
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Artikelen 1–20