Follow
Sinéad Cullina
Sinéad Cullina
Verified email at icahn.mssm.edu
Title
Cited by
Cited by
Year
Genetic analyses of diverse populations improves discovery for complex traits
GL Wojcik, M Graff, KK Nishimura, R Tao, J Haessler, CR Gignoux, ...
Nature 570 (7762), 514-518, 2019
7642019
Toward a fine-scale population health monitoring system
GM Belbin, S Cullina, S Wenric, ER Soper, BS Glicksberg, D Torre, ...
Cell 184 (8), 2068-2083. e11, 2021
972021
Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank
NS Abul-Husn, ER Soper, JA Odgis, S Cullina, D Bobo, A Moscati, ...
Genome Medicine 12, 1-12, 2020
912020
Implementing genomic screening in diverse populations
NS Abul-Husn, ER Soper, GT Braganza, JE Rodriguez, N Zeid, S Cullina, ...
Genome medicine 13, 1-11, 2021
472021
The page study: how genetic diversity improves our understanding of the architecture of complex traits
GL Wojcik, M Graff, KK Nishimura, R Tao, J Haessler, CR Gignoux, ...
212017
Regeneron Genetics Center; Loos, RJF; et al
NS Abul-Husn, ER Soper, JA Odgis, S Cullina, D Bobo, A Moscati, ...
Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder …, 2019
142019
Lynch Syndrome–Associated Variants and Cancer Rates in an Ancestrally Diverse Biobank
RE Rosenblum, C Ang, SA Suckiel, ER Soper, MR Sigireddi, S Cullina, ...
JCO Precision Oncology 1, 1429-1444, 2020
92020
CDH1 pathogenic variants and cancer risk in an unselected patient population
A Bar-Mashiah, ER Soper, S Cullina, GM Belbin, EE Kenny, AL Lucas, ...
Familial cancer 21 (2), 235-239, 2022
62022
Leveraging health systems data to characterize a large effect variant conferring risk for liver disease in Puerto Ricans
GM Belbin, S Rutledge, T Dodatko, S Cullina, MC Turchin, S Kohli, ...
The American Journal of Human Genetics 108 (11), 2099-2111, 2021
32021
Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35
S Cullina, GL Wojcik, R Shemirani, D Klarin, BR Gorman, EP Sorokin, ...
Frontiers in Genetics 14, 1181167, 2023
22023
Genetic identification and characterization of Lynch syndrome in a multi-ethnic biobank.
R Rosenblum, SA Suckiel, GM Belbin, S Cullina, JH Cho, EE Kenny, ...
Journal of Clinical Oncology 37 (15_suppl), 1520-1520, 2019
22019
Genotype-First Analysis of TTR Variant Carriers Identifies Novel Traits Associated With Heritable Amyloidosis
AR Kontorovich, A McClellan, S Cullina, G Belbin, P Gorevic, E Kenny, ...
Circulation 140 (Suppl_1), A13496-A13496, 2019
12019
The genetic underpinnings of variable penetrance and expressivity of pathogenic mutations in cardiometabolic traits
A Wei, R Border, B Fu, S Cullina, N Brandes, S Sankararaman, EE Kenny, ...
medRxiv, 2023.09. 14.23295564, 2023
2023
TOPORS as a novel causal gene for Joubert syndrome
A Strong, HQ Qu, S Cullina, ML McManus, EH Zackai, J Glessner, ...
American Journal of Medical Genetics Part A 191 (8), 2156-2163, 2023
2023
Sequencing-based screening for lysosomal disorders in a multi-ethnic biobank
A Iverson, GM Belbin, S Cullina, EE Kenny, M Balwani, NS Abul-Husn
Molecular Genetics and Metabolism 129 (2), S79, 2020
2020
Exome Sequencing Reveals a High Prevalence ofBRCA1andBRCA2Founder Variants in a Diverse Population-Based Biobank
NS Abul-Husn, ER Soper, JA Odgis, S Cullina, D Bobo, A Moscati, ...
2019
LOWER PREVALENCE OF HSD17B13 NASH PROTECTIVE VARIANT FOUND AMONG WOMEN WITH GESTATIONAL DIABETES MELLITUS
T Kushner, A Merkelson, S Cullina, G Belbin, SL Friedman, K Sigel, ...
HEPATOLOGY 70, 1134A-1135A, 2019
2019
SUN-032 Exome Sequencing Reveals that Pathogenic RET Variants Occur at Higher Prevalence Than Previously Recognized: Data from a US Health System Biobank
H Guzman, E Gallagher, G Belbin, S Cullina, R Haber, J Cho, E Kenny, ...
Journal of the Endocrine Society 3 (Supplement_1), SUN-032, 2019
2019
The system can't perform the operation now. Try again later.
Articles 1–18