|Genome-wide analysis of mammalian promoter architecture and evolution|
P Carninci, A Sandelin, B Lenhard, S Katayama, K Shimokawa, ...
Nature genetics 38 (6), 626-635, 2006
|Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways|
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
Science 347 (6229), 1436-1441, 2015
|α-Synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity|
AD Gitler, A Chesi, ML Geddie, KE Strathearn, S Hamamichi, KJ Hill, ...
Nature genetics 41 (3), 308-315, 2009
|Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLS|
Z Sun, Z Diaz, X Fang, MP Hart, A Chesi, J Shorter, AD Gitler
PLoS biology 9 (4), e1000614, 2011
|Genome-wide analyses identify KIF5A as a novel ALS gene|
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
|Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index|
JF Felix, JP Bradfield, C Monnereau, RJP Van Der Valk, E Stergiakouli, ...
Human molecular genetics 25 (2), 389-403, 2016
|Life-course genome-wide association study meta-analysis of total body BMD and assessment of age-specific effects|
C Medina-Gomez, JP Kemp, K Trajanoska, J Luan, A Chesi, TS Ahluwalia, ...
The American Journal of Human Genetics 102 (1), 88-102, 2018
|CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia|
KL Williams, S Topp, S Yang, B Smith, JA Fifita, ST Warraich, KY Zhang, ...
Nature communications 7 (1), 11253, 2016
|Exome sequencing to identify de novo mutations in sporadic ALS trios|
A Chesi, BT Staahl, A Jovičić, J Couthouis, M Fasolino, AR Raphael, ...
Nature neuroscience 16 (7), 851-855, 2013
|Infant BMI or weight-for-length and obesity risk in early childhood|
SM Roy, JG Spivack, MS Faith, A Chesi, JA Mitchell, A Kelly, SFA Grant, ...
Pediatrics 137 (5), 2016
|Inhibition of α-synuclein fibrillization by dopamine is mediated by interactions with five C-terminal residues and with E83 in the NAC region|
FE Herrera, A Chesi, KE Paleologou, A Schmid, A Munoz, M Vendruscolo, ...
PLoS One 3 (10), e3394, 2008
|A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories|
C Akimoto, AE Volk, M van Blitterswijk, M Van den Broeck, CS Leblond, ...
Journal of medical genetics 51 (6), 419-424, 2014
|Association between linear growth and bone accrual in a diverse cohort of children and adolescents|
SE McCormack, DL Cousminer, A Chesi, JA Mitchell, SM Roy, ...
JAMA pediatrics 171 (9), e171769-e171769, 2017
|The genetics of pediatric obesity|
A Chesi, SFA Grant
Trends in Endocrinology & Metabolism 26 (12), 711-721, 2015
|First genome-wide association study of latent autoimmune diabetes in adults reveals novel insights linking immune and metabolic diabetes|
DL Cousminer, E Ahlqvist, R Mishra, MK Andersen, A Chesi, MI Hawa, ...
Diabetes care 41 (11), 2396-2403, 2018
|Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry …|
MCY Ng, M Graff, Y Lu, AE Justice, P Mudgal, CT Liu, K Young, LR Yanek, ...
PLoS genetics 13 (4), e1006719, 2017
|Genome-scale Capture C promoter interactions implicate effector genes at GWAS loci for bone mineral density|
A Chesi, Y Wagley, ME Johnson, E Manduchi, C Su, S Lu, ME Leonard, ...
Nature Communications 10 (1), 1260, 2019
|Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes|
R Mishra, A Chesi, DL Cousminer, MI Hawa, JP Bradfield, KM Hodge, ...
BMC medicine 15, 1-10, 2017
|Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus|
C Medina-Gomez, JP Kemp, NL Dimou, E Kreiner, A Chesi, BS Zemel, ...
Nature communications 8 (1), 121, 2017
|The type 2 diabetes presumed causal variant within TCF7L2 resides in an element that controls the expression of ACSL5|
Q Xia, A Chesi, E Manduchi, BT Johnston, S Lu, ME Leonard, UW Parlin, ...
Diabetologia 59, 2360-2368, 2016