Laura Sloofman
Laura Sloofman
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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
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
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
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
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
Neuromolecular responses to social challenge: Common mechanisms across mouse, stickleback fish, and honey bee
CC Rittschof, SA Bukhari, LG Sloofman, JM Troy, D Caetano-AnollÚs, ...
Proceedings of the national Academy of Sciences 111 (50), 17929-17934, 2014
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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