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Jennifer Asimit
Jennifer Asimit
MRC Biostatistics Unit, University of Cambridge
Verified email at mrc-bsu.cam.ac.uk - Homepage
Title
Cited by
Cited by
Year
The African genome variation project shapes medical genetics in Africa
D Gurdasani, T Carstensen, F Tekola-Ayele, L Pagani, I Tachmazidou, ...
Nature 517 (7534), 327-332, 2015
6172015
Rare variant association analysis methods for complex traits
J Asimit, E Zeggini
Annual review of genetics 44, 293-308, 2010
3232010
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
AR Majithia, J Flannick, P Shahinian, M Guo, MA Bray, P Fontanillas, ...
Proceedings of the National Academy of Sciences 111 (36), 13127-13132, 2014
1772014
A combined functional annotation score for non-synonymous variants
MC Lopes, C Joyce, GRS Ritchie, SL John, F Cunningham, J Asimit, ...
Human heredity 73 (1), 47-51, 2012
1072012
Trans-ethnic study design approaches for fine-mapping
JL Asimit, K Hatzikotoulas, M McCarthy, AP Morris, E Zeggini
European journal of human genetics 24 (9), 1330-1336, 2016
932016
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data
JL Asimit, AG Day-Williams, AP Morris, E Zeggini
Human heredity 73 (2), 84-94, 2012
732012
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations
Y Xue, M Mezzavilla, M Haber, S McCarthy, Y Chen, V Narasimhan, ...
Nature communications 8 (1), 15927, 2017
722017
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
M Schmidts, Y Hou, CR Cortés, DA Mans, C Huber, K Boldt, M Patel, ...
Nature communications 6 (1), 7074, 2015
542015
Genome‐wide association analysis of imputed rare variants: application to seven common complex diseases
R Mägi, JL Asimit, AG Day‐Williams, E Zeggini, AP Morris
Genetic epidemiology 36 (8), 785-796, 2012
402012
Fine-mapping genetic associations
A Hutchinson, J Asimit, C Wallace
Human Molecular Genetics 29 (R1), R81-R88, 2020
382020
Stochastic search and joint fine-mapping increases accuracy and identifies previously unreported associations in immune-mediated diseases
JL Asimit, DB Rainbow, MD Fortune, NF Grinberg, LS Wicker, C Wallace
Nature communications 10 (1), 3216, 2019
272019
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms
M Horikoshi, L Pasquali, S Wiltshire, JR Huyghe, A Mahajan, JL Asimit, ...
Human molecular genetics 25 (10), 2070-2081, 2016
262016
Defining the power limits of genome‐wide association scan meta‐analyses
K Chapman, T Ferreira, A Morris, J Asimit, E Zeggini
Genetic epidemiology 35 (8), 781-789, 2011
242011
Gene‐or region‐based analysis of genome‐wide association studies
J Beyene, D Tritchler, JL Asimit, JS Hamid
Genetic Epidemiology 33 (S1), S105-S110, 2009
222009
An evaluation of different meta-analysis approaches in the presence of allelic heterogeneity
J Asimit, A Day-Williams, L Zgaga, I Rudan, V Boraska, E Zeggini
European Journal of Human Genetics 20 (6), 709-712, 2012
212012
Testing for rare variant associations in complex diseases
J Asimit, E Zeggini
Genome medicine 3, 1-3, 2011
182011
Imputation of rare variants in next-generation association studies
JL Asimit, E Zeggini
Human heredity 74 (3-4), 196-204, 2013
172013
The flashfm approach for fine-mapping multiple quantitative traits
N Hernández, J Soenksen, P Newcombe, M Sandhu, I Barroso, ...
Nature communications 12 (1), 1-14, 2021
122021
Region-based analysis in genome-wide association study of Framingham Heart Study blood lipid phenotypes
JL Asimit, YJ Yoo, D Waggott, L Sun, SB Bull
BMC proceedings 3, 1-5, 2009
102009
Parametric modeling of reaction time experiment data
WJ Braun, V Rousson, WA Simpson, J Prokop
Biometrics 59 (3), 661-669, 2003
102003
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