World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
47
Citations
21951
World Ranking
4080
National Ranking
1759

Overview

Lauren A. Weiss is affiliated with the University of California, San Francisco in the United States. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, and Medicine. Within these domains, Weiss's subfields of study include Genetics, Molecular Biology, Cognitive Neuroscience, Pediatrics, Perinatology and Child Health, and Experimental and Cognitive Psychology.

The scientist's work concentrates on several main topics, including Genetic Associations and Epidemiology, Genomic variations and chromosomal abnormalities, Congenital heart defects research, Autism Spectrum Disorder Research, Epigenetics and DNA Methylation, Genetics and Neurodevelopmental Disorders, and Cognitive Abilities and Testing.

Recent publications by Weiss include the following papers:

  • Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits, 2021, Biological Psychiatry
  • Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p, 2022, Nature Genetics
  • Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes, 2021, Genome Medicine
  • Can the "female protective effect" liability threshold model explain sex differences in autism spectrum disorder?, 2022, Neuron
  • Examining Sex Differences in Autism Heritability, 2024, JAMA Psychiatry

Frequent co-authors collaborating with Weiss are Michela Traglia, Lisa Croen, Jakob Grove, Thomas Werge, and Mikhail Vysotskiy.

The most common venues for Weiss's publications include bioRxiv (Cold Spring Harbor Laboratory), PLoS Genetics, UNC Libraries, Biological Psychiatry, and Nature Genetics.

Best Publications

  • Synaptic, transcriptional and chromatin genes disrupted in autism

    Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney

  • Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    F. Kyle Satterstrom;F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S. Breen

  • Association between Microdeletion and Microduplication at 16p11.2 and Autism

    Lauren A. Weiss;Yiping Shen;Joshua M. Korn;Joshua M. Korn;Dan E. Arking

  • Analysis of shared heritability in common disorders of the brain

    Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters

  • Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

    Phil H. Lee;Verneri Anttila;Hyejung Won;Yen-Chen A. Feng

  • Association between microdeletion and microduplication at 16p11.2 and autism

    Lauren A. Weiss;Yiping Shen;Joshua M. Korn;Dan E. Arking

  • SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

    Brett S Abrahams;Dan E Arking;Daniel B Campbell;Heather C Mefford

  • A genome-wide linkage and association scan reveals novel loci for autism

    Lauren A. Weiss;Lauren A. Weiss;Dan E. Arking;Mark J. Daly;Mark J. Daly;Aravinda Chakravarti

  • Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

    Richard J.L. Anney;Richard J.L. Anney;Stephan Ripke;Stephan Ripke;Stephan Ripke;Verneri Anttila;Jakob Grove;Jakob Grove

  • Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

    Colm O'Dushlaine;Lizzy Rossin;Phil H. Lee;Laramie Duncan;Laramie Duncan

  • Disruption of Neurexin 1 Associated with Autism Spectrum Disorder

    Hyung Goo Kim;Shotaro Kishikawa;Anne W. Higgins;Ihn Sik Seong

  • Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S Breen;Michael S Breen

  • The sex-specific genetic architecture of quantitative traits in humans

    Lauren A Weiss;Lauren A Weiss;Lin Pan;Mark Abney;Carole Ober

  • Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

    David T. Miller;Yiping Shen;Lauren A. Weiss;Joshua Korn

  • Ratio of n−6 to n−3 fatty acids and bone mineral density in older adults: the Rancho Bernardo Study

    Lauren A Weiss;Elizabeth Barrett-Connor;Denise von Mühlen

  • Sodium channels SCN1A, SCN2A and SCN3A in familial autism.

    L A Weiss;A Escayg;J A Kearney;M Trudeau

  • Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder

    Elaine T Lim;Mohammed Uddin;Silvia De Rubeis;Yingleong Chan;Yingleong Chan

  • Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

    Robert Maier;Gerhard Moser;Guo-Bo Chen;Stephan Ripke

  • Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages.

    Maggie L. Chow;Tiziano Pramparo;Tiziano Pramparo;Mary E. Winn;Mary E. Winn;Cynthia Carter Barnes

  • Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

    Lee Ph;Anttila;Won H

Frequent Co-Authors

Christopher A. Walsh
Christopher A. Walsh Howard Hughes Medical Institute
Mark J. Daly
Mark J. Daly Massachusetts General Hospital
Benjamin M. Neale
Benjamin M. Neale Harvard University
Edwin H. Cook
Edwin H. Cook University of Illinois at Chicago
Thomas Werge
Thomas Werge University of Copenhagen
Stephen W. Scherer
Stephen W. Scherer University of Toronto
Joseph D. Buxbaum
Joseph D. Buxbaum Icahn School of Medicine at Mount Sinai
Aarno Palotie
Aarno Palotie University of Helsinki
Catalina Betancur
Catalina Betancur Sorbonne University
Anders D. Børglum
Anders D. Børglum Aarhus University

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