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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
11462021
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
8582021
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
3682022
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
3122022
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
2292019
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
1982022
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
1672014
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
1562018
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
1382018
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
672020
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
662017
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
592020
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
512017
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
502017
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
482022
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
462022
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
422021
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
382019
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
372021
Deficiency in perlecan/HSPG2 during bone development enhances osteogenesis and decreases quality of adult bone in mice
DA Lowe, N Lepori-Bui, PV Fomin, LG Sloofman, X Zhou, ...
Calcified tissue international 95, 29-38, 2014
342014
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