|Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort|
L Shen, S Kim, SL Risacher, K Nho, S Swaminathan, JD West, T Foroud, ...
Neuroimage 53 (3), 1051-1063, 2010
|Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans|
AJ Saykin, L Shen, TM Foroud, SG Potkin, S Swaminathan, S Kim, ...
Alzheimer's & dementia 6 (3), 265-273, 2010
|Genome-wide association study of CSF biomarkers Aâ1-42, t-tau, and p-tau181p in the ADNI cohort|
S Kim, S Swaminathan, L Shen, SL Risacher, K Nho, T Foroud, LM Shaw, ...
Neurology 76 (1), 69-79, 2011
|APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study|
VK Ramanan, SL Risacher, K Nho, S Kim, S Swaminathan, L Shen, ...
Molecular psychiatry 19 (3), 351, 2014
|Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers|
L Shen, PM Thompson, SG Potkin, L Bertram, LA Farrer, TM Foroud, ...
Brain imaging and behavior 8 (2), 183-207, 2014
|Effect of complement CR1 on brain amyloid burden during aging and its modification by APOE genotype|
M Thambisetty, Y An, M Nalls, J Sojkova, S Swaminathan, Y Zhou, ...
Biological psychiatry 73 (5), 422-428, 2013
|Genomic copy number analysis in Alzheimer's disease and mild cognitive impairment: an ADNI study|
S Swaminathan, S Kim, L Shen, SL Risacher, T Foroud, N Pankratz, ...
International Journal of Alzheimer˘s Disease 2011, 2011
|Analysis of copy number variation in Alzheimer's disease: the NIALOAD/NCRAD Family Study|
S Swaminathan, L Shen, S Kim, M Inlow, J D West, K M Faber, T Foroud, ...
Current Alzheimer Research 9 (7), 801-814, 2012
|Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel|
S Kim, S Swaminathan, M Inlow, SL Risacher, K Nho, L Shen, TM Foroud, ...
PloS one 8 (7), e70269, 2013
|Amyloid pathway-based candidate gene analysis of [11C]PiB-PET in the Alzheimer˘s Disease Neuroimaging Initiative (ADNI) cohort|
S Swaminathan, L Shen, SL Risacher, KK Yoder, JD West, S Kim, K Nho, ...
Brain imaging and behavior 6 (1), 1-15, 2012
|Identifying neuroimaging and proteomic biomarkers for MCI and AD via the elastic net|
L Shen, S Kim, Y Qi, M Inlow, S Swaminathan, K Nho, J Wan, SL Risacher, ...
International Workshop on Multimodal Brain Image Analysis, 27-34, 2011
|Protective variant for hippocampal atrophy identified by whole exome sequencing|
K Nho, S Kim, SL Risacher, L Shen, JJ Corneveaux, S Swaminathan, ...
Annals of neurology 77 (3), 547-552, 2015
|Association of plasma and cortical amyloid beta is modulated by APOE ĺ4 status|
S Swaminathan, SL Risacher, KK Yoder, JD West, L Shen, S Kim, M Inlow, ...
Alzheimer's & Dementia 10 (1), e9-e18, 2014
|Hippocampal surface mapping of genetic risk factors in AD via sparse learning models|
J Wan, S Kim, M Inlow, K Nho, S Swaminathan, SL Risacher, S Fang, ...
International Conference on Medical Image Computing and Computer-Assisted …, 2011
|Analysis of copy number variation in Alzheimer˘s disease in a cohort of clinically characterized and neuropathologically verified individuals|
S Swaminathan, MJ Huentelman, JJ Corneveaux, AJ Myers, KM Faber, ...
PLoS One 7 (12), e50640, 2012
|A frame-shift mutation in CAV1 is associated with a severe neonatal progeroid and lipodystrophy syndrome|
I Schrauwen, S Szelinger, AL Siniard, A Kurdoglu, JJ Corneveaux, ...
PLoS One 10 (7), e0131797, 2015
|A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20|
NA Hanchard, S Swaminathan, K Bucasas, D Furthner, S Fernbach, ...
Human molecular genetics 25 (11), 2331-2341, 2016
|A de novo mutation in TEAD1 causes non–X-linked Aicardi syndrome|
I Schrauwen, S Szelinger, AL Siniard, JJ Corneveaux, A Kurdoglu, ...
Investigative ophthalmology & visual science 56 (6), 3896-3904, 2015
|The effect of reference panels and software tools on genotype imputation|
K Nho, L Shen, S Kim, S Swaminathan, SL Risacher, AJ Saykin, ...
AMIA Annual Symposium Proceedings 2011, 1013, 2011
|Whole-Exome Sequencing Reveals Uncaptured Variation and Distinct Ancestry in the Southern African Population of Botswana|
G Retshabile, BC Mlotshwa, L Williams, S Mwesigwa, G Mboowa, ...
The American Journal of Human Genetics 102 (5), 731-743, 2018