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Laura Sloofman
Laura Sloofman
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Cited by
Year
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
N Mullins, AJ Forstner, KS O’Connell, B Coombes, JRI Coleman, Z Qiao, ...
Nature genetics 53 (6), 817-829, 2021
8442021
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
7882021
Whole-genome sequencing reveals host factors underlying critical COVID-19
A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ...
Nature 607 (7917), 97-103, 2022
2472022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ...
Nature genetics 54 (9), 1320-1331, 2022
2272022
CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder
GE Hoffman, J Bendl, G Voloudakis, KS Montgomery, L Sloofman, ...
Scientific data 6 (1), 180, 2019
1892019
Neuromolecular responses to social challenge: common mechanisms across mouse, stickleback fish, and honey bee
CC Rittschof, SA Bukhari, LG Sloofman, JM Troy, D Caetano-Anollés, ...
Proceedings of the national Academy of Sciences 111 (50), 17929-17934, 2014
1592014
Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors
N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ...
Biological psychiatry 91 (3), 313-327, 2022
1512022
Landscape of conditional eQTL in dorsolateral prefrontal cortex and co-localization with schizophrenia GWAS
A Dobbyn, LM Huckins, J Boocock, LG Sloofman, BS Glicksberg, ...
The American Journal of Human Genetics 102 (6), 1169-1184, 2018
1402018
Cell-specific histone modification maps in the human frontal lobe link schizophrenia risk to the neuronal epigenome
K Girdhar, GE Hoffman, Y Jiang, L Brown, M Kundakovic, ME Hauberg, ...
Nature neuroscience 21 (8), 1126-1136, 2018
1232018
Behavioral, transcriptomic and epigenetic responses to social challenge in honey bees
HY Shpigler, MC Saul, EE Murdoch, AC Cash‐Ahmed, CH Seward, ...
Genes, Brain and Behavior 16 (6), 579-591, 2017
612017
Analysis of genetically regulated gene expression identifies a prefrontal PTSD gene, SNRNP35, specific to military cohorts
LM Huckins, C Chatzinakos, MS Breen, J Hartmann, T Klengel, ...
Cell reports 31 (9), 2020
572020
Transcriptional regulatory dynamics drive coordinated metabolic and neural response to social challenge in mice
MC Saul, CH Seward, JM Troy, H Zhang, LG Sloofman, X Lu, PA Weisner, ...
Genome research 27 (6), 959-972, 2017
482017
SMARCAD1 contributes to the regulation of naive pluripotency by interacting with histone citrullination
S Xiao, J Lu, B Sridhar, X Cao, P Yu, T Zhao, CC Chen, D McDee, ...
Cell reports 18 (13), 3117-3128, 2017
482017
Functional annotation of rare structural variation in the human brain
L Han, X Zhao, ML Benton, T Perumal, RL Collins, GE Hoffman, ...
Nature communications 11 (1), 2990, 2020
452020
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
G Butler-Laporte, G Povysil, JA Kosmicki, ET Cirulli, T Drivas, S Furini, ...
PLoS genetics 18 (11), e1010367, 2022
362022
Chromatin domain alterations linked to 3D genome organization in a large cohort of schizophrenia and bipolar disorder brains
K Girdhar, GE Hoffman, J Bendl, S Rahman, P Dong, W Liao, ...
Nature neuroscience 25 (4), 474-483, 2022
362022
Cross‐species systems analysis of evolutionary toolkits of neurogenomic response to social challenge
MC Saul, C Blatti, W Yang, SA Bukhari, HY Shpigler, JM Troy, CH Seward, ...
Genes, Brain and Behavior 18 (1), e12502, 2019
352019
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, L Klei, ...
MedRxiv, 2021.12. 20.21267194, 2021
342021
Ribosomal protein L29/HIP deficiency delays osteogenesis and increases fragility of adult bone in mice
DS Oristian, LG Sloofman, X Zhou, L Wang, MC Farach‐Carson, ...
Journal of Orthopaedic Research 27 (1), 28-35, 2009
332009
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
M D’Antonio, JP Nguyen, TD Arthur, H Matsui, BM Neale, M Daly, ...
Cell reports 37 (7), 2021
302021
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