Author details

Full Name

Laura M Huckins

Affiliation

ORCID

Career Start Year

2013

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34493831	Induction of dopaminergic neurons for neuronal subtype-specific modeling of psychiatric disease risk.	Mol Psychiatry	2023
35379376	Mapping anorexia nervosa genes to clinical phenotypes.	Psychol Med	2023
37766803	Trauma Matters: Integrating Genetic and Environmental Components of PTSD.		2023
37678542	Genetically Regulated Gene Expression in the Brain Associated With Chronic Pain: Relationships With Clinical Traits and Potential for Drug Repurposing.		2023
37905000	Genomic insights into the comorbidity between type 2 diabetes and schizophrenia.	medRxiv	2023
37693435	Comorbidity Profiles of Posttraumatic Stress Disorder Across the Medical Phenome.	medRxiv	2023
37032718	Thoughtful Phenotype Definitions Empower Participants and Power Studies.		2023
36711574	Transcriptional signatures of heroin intake and seeking throughout the brain reward circuit.		2023
37076454	Integrating genetics and transcriptomics to study major depressive disorder: a conceptual framework, bioinformatic approaches, and recent findings.		2023
36993466	Non-additive effects of schizophrenia risk genes reflect convergent downstream function.		2023
37294757	Transcriptional signatures of heroin intake and relapse throughout the brain reward circuitry in male mice.		2023
37034825	Chronic Pain and Psychiatric Conditions.		2023
36658083	Stem Cell Models for Context-Specific Modeling in Psychiatric Disorders.		2023
35177824	Altered gene expression and PTSD symptom dimensions in World Trade Center responders.	Mol Psychiatry	2022
35931093	Concerns about the use of polygenic embryo screening for psychiatric and cognitive traits.	Lancet Psychiatry	2022
35780037	Exploring the clinical and genetic associations of adult weight trajectories using electronic health records in a racially diverse biobank: a phenome-wide and polygenic risk study.	Lancet Digit Health	2022
35595976	What next for eating disorder genetics? Replacing myths with facts to sharpen our understanding.	Mol Psychiatry	2022
36506088	Reduced expression in transcriptome of human iPSC-derived neural progenitors modeling fragile X syndrome.		2022
35181757	Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder.	Mol Psychiatry	2022
35115012	Comparison of confound adjustment methods in the construction of gene co-expression networks.		2022
35263625	Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.	Am J Hum Genet	2022
34642700	Acute COVID-19 gene-expression profiles show multiple etiologies of long-term sequelae.	medRxiv	2021
32064741	Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.	Addict Biol	2021
33636110	Common Genetic Variation in Humans Impacts In Vitro Susceptibility to SARS-CoV-2 Infection.	Stem Cell Reports	2021
34002096	Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.	Nat Genet	2021
34107879	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	BMC Genomics	2021
34517814	Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.	BMC Genomics	2021
32995783	Common genetic variation in humans impacts in vitro susceptibility to SARS-CoV-2 infection.	bioRxiv	2020
32075678	A chromosomal connectome for psychiatric and metabolic risk variants in adult dopaminergic neurons.	Genome Med	2020
32492425	Analysis of Genetically Regulated Gene Expression Identifies a Prefrontal PTSD Gene, SNRNP35, Specific to Military Cohorts.	Cell Rep	2020
32879975	Implicit bias of encoded variables: frameworks for addressing structured bias in EHR-GWAS data.	Human Molecular Genetics	2020
33199899	Massively parallel techniques for cataloguing the regulome of the human brain.	Nature Neuroscience	2020
33247020	Retrospective cohort study of clinical characteristics of 2199 hospitalised patients with COVID-19 in New York City.	BMJ Open	2020
33027032	Machine Learning to Predict Mortality and Critical Events in a Cohort of Patients With COVID-19 in New York City: Model Development and Validation.	J Med Internet Res	2020
32511655	Clinical Characteristics of Hospitalized Covid-19 Patients in New York City.	medRxiv	2020
31374203	Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.	Am J Hum Genet	2019
31086353	Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.	Nat Genet	2019
31217584	Genetic analyses of diverse populations improves discovery for complex traits.	Nature	2019
31124312	International Society of Psychiatric Genetics Ethics Committee: Issues facing us.	Am J Med Genet B Neuropsychiatr Genet	2019
31209380	Genome-wide association study implicates CHRNA2 in cannabis use disorder.	Nat Neurosci	2019
31160808	Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.	Nat Genet	2019
31548722	Synergistic effects of common schizophrenia risk variants.	Nat Genet	2019
29805045	Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS.	Am J Hum Genet	2018
29930110	Analysis of shared heritability in common disorders of the brain.	Science	2018
30420737	Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.	Mol Psychiatry	2018
29623448	Recent Genetics and Epigenetics Approaches to PTSD.	Curr Psychiatry Rep	2018
29483656	Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.	Nat Genet	2018
29739930	Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.	Nat Commun	2018
29155802	Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.	Mol Psychiatry	2018
29262854	Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.	Genome Med	2017