Follow
Erin Heinzen
Erin Heinzen
Associate Professor, Eshelman School of Pharmacy
Verified email at unc.edu
Title
Cited by
Cited by
Year
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
44982009
De novo mutations in epileptic encephalopathies
Nature 501 (7466), 217-221, 2013
1461*2013
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13472018
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
10722011
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), e1003709, 2013
10072013
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), e1000373, 2009
5582009
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
4832012
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
4022012
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
3162014
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), e1000001, 2008
3072008
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
2792010
De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies
CT Myers, JM McMahon, AL Schneider, S Petrovski, AS Allen, GL Carvill, ...
The American Journal of Human Genetics 99 (2), 287-298, 2016
2472016
Distinct neurological disorders with ATP1A3 mutations
EL Heinzen, A Arzimanoglou, A Brashear, SJ Clapcote, F Gurrieri, ...
The Lancet Neurology 13 (5), 503-514, 2014
2362014
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
2242019
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
2082012
A roadmap for precision medicine in the epilepsies
EpiPM Consortium
The Lancet Neurology 14 (12), 1219-1228, 2015
2032015
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), e1001111, 2010
1972010
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), e1000781, 2010
1922010
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ...
Nature genetics 51 (1), 117-127, 2019
1902019
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
1812010
The system can't perform the operation now. Try again later.
Articles 1–20