| Large recurrent microdeletions associated with schizophrenia H Stefansson, D Rujescu, S Cichon, OPH Pietiläinen, A Ingason, ... nature 455 (7210), 232-236, 2008 | 3643* | 2008 |
| Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence JE Savage, PR Jansen, S Stringer, K Watanabe, J Bryois, CA De Leeuw, ... Nature genetics 50 (7), 912-919, 2018 | 1111 | 2018 |
| A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci SG Pillai, D Ge, G Zhu, X Kong, KV Shianna, AC Need, S Feng, CP Hersh, ... PLoS genetics 5 (3), e1000421, 2009 | 851 | 2009 |
| Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function G Davies, M Lam, SE Harris, JW Trampush, M Luciano, WD Hill, ... Nature communications 9 (1), 2098, 2018 | 617 | 2018 |
| 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 | 562 | 2009 |
| Clinical application of exome sequencing in undiagnosed genetic conditions AC Need, V Shashi, Y Hitomi, K Schoch, KV Shianna, MT McDonald, ... Journal of medical genetics 49 (6), 353-361, 2012 | 509 | 2012 |
| Long-range LD can confound genome scans in admixed populations AL Price, ME Weale, N Patterson, SR Myers, AC Need, KV Shianna, D Ge, ... The American Journal of Human Genetics 83 (1), 132-135, 2008 | 475 | 2008 |
| Next generation disparities in human genomics: concerns and remedies AC Need, DB Goldstein Trends in Genetics 25 (11), 489-494, 2009 | 426 | 2009 |
| 100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report 100,000 Genomes Project Pilot Investigators New England Journal of Medicine 385 (20), 1868-1880, 2021 | 388 | 2021 |
| Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios X Zhu, S Petrovski, P Xie, EK Ruzzo, YF Lu, K McSweeney, B Ben-Zeev, ... Genetics in Medicine 17 (10), 774-781, 2015 | 361 | 2015 |
| The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders V Shashi, A McConkie-Rosell, B Rosell, K Schoch, K Vellore, ... Genetics in Medicine 16 (2), 176-182, 2014 | 324 | 2014 |
| GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium JW Trampush, MLZ Yang, J Yu, E Knowles, G Davies, DC Liewald, ... Molecular psychiatry 22 (3), 336-345, 2017 | 288 | 2017 |
| 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 | 279 | 2010 |
| Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway GM Enns, V Shashi, M Bainbridge, MJ Gambello, FR Zahir, T Bast, ... Genetics in Medicine 16 (10), 751-758, 2014 | 230 | 2014 |
| Temporal lobe functional activity and connectivity in young adult APOE ɛ4 carriers NA Dennis, JN Browndyke, J Stokes, A Need, JR Burke, ... Alzheimer's & Dementia 6 (4), 303-311, 2010 | 225 | 2010 |
| 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 | 198 | 2010 |
| A comparison of the Cambridge Automated Neuropsychological Test Battery (CANTAB) with “traditional” neuropsychological testing instruments PJ Smith, AC Need, ET Cirulli, O Chiba-Falek, DK Attix Journal of clinical and experimental neuropsychology 35 (3), 319-328, 2013 | 197 | 2013 |
| WGAViewer: software for genomic annotation of whole genome association studies D Ge, K Zhang, AC Need, O Martin, J Fellay, TJ Urban, A Telenti, ... Genome Research 18 (4), 640-643, 2008 | 196 | 2008 |
| One gene, many neuropsychiatric disorders: lessons from Mendelian diseases X Zhu, AC Need, S Petrovski, DB Goldstein Nature neuroscience 17 (6), 773-781, 2014 | 194 | 2014 |
| Copy number variation of KIR genes influences HIV-1 control K Pelak, AC Need, J Fellay, KV Shianna, S Feng, TJ Urban, D Ge, ... PLoS biology 9 (11), e1001208, 2011 | 185 | 2011 |
Erin HeinzenAssociate Professor, Eshelman School of Pharmacy在 unc.edu 的电子邮件经过验证
Erin HeinzenAssociate Professor, Eshelman School of Pharmacy在 unc.edu 的电子邮件经过验证