Anna Need
Anna Need
Geverifieerd e-mailadres voor imperial.ac.uk
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Large recurrent microdeletions associated with schizophrenia
H Stefansson, D Rujescu, S Cichon, OPH Pietilšinen, A Ingason, ...
nature 455 (7210), 232-236, 2008
3130*2008
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 Genet 5 (3), e1000421, 2009
6872009
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 Genet 5 (2), e1000373, 2009
5032009
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
3932012
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
3172018
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
2712008
Next generation disparities in human genomics: concerns and remedies
AC Need, DB Goldstein
Trends in Genetics 25 (11), 489-494, 2009
2532009
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
2482010
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios
X Zhu, S Petrovski, P Xie, EK Ruzzo, YF Lu, KM McSweeney, B Ben-Zeev, ...
Genetics in Medicine 17 (10), 774-781, 2015
2252015
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
2102014
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
1872008
The characterization of twenty sequenced human genomes
K Pelak, KV Shianna, D Ge, JM Maia, M Zhu, JP Smith, ET Cirulli, J Fellay, ...
PLoS Genet 6 (9), e1001111, 2010
1782010
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
1782010
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), 1-16, 2018
1702018
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 Biol 9 (11), e1001208, 2011
1552011
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
1532009
Priorities and standards in pharmacogenetic research
AC Need, AG Motulsky, DB Goldstein
Nature genetics 37 (7), 671-681, 2005
1482005
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
1442017
One gene, many neuropsychiatric disorders: lessons from Mendelian diseases
X Zhu, AC Need, S Petrovski, DB Goldstein
Nature neuroscience 17 (6), 773, 2014
1392014
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
1312014
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Artikelen 1–20