Laura T. Jiménez-Barrón

发表

Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine

Han Fang, David Mittelman, Gholson J. Lyon, 2017, BMC Medical Genomics.

Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline

I. Iossifov, G. Lyon, Han Fang, 2015, bioRxiv.

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations

Edward Yang, Laurence Faivre, Jillian S Parboosingh, 2015, American journal of human genetics.

Quantifying Absolute Protein Synthesis Rates Reveals Principles Underlying Allocation of Cellular Resources

Laura T. Jiménez-Barrón, Laura Jimenez-Barron, 2014 .

Human-specific enrichment of schizophrenia risk-genes in callosal neurons of the developing neocortex

J. Levin, S. Lodato, P. Arlotta, 2021, bioRxiv.

Genome Wide Variant Analysis of Simplex Autism Families with an Integrative Clinical-Bioinformatics Pipeline

I. Iossifov, G. Lyon, Han Fang, 2015, bioRxiv.

Whole genome analysis of an extended pedigree with Prader–Willi Syndrome, hereditary hemochromatosis, and dysautonomia-like symptoms

G. Highnam, D. Mittelman, G. Lyon, 2015, bioRxiv.

Building Genomic Analysis Pipelines in a Hackathon Setting with Bioinformatician Teams: DNA-seq, Epigenomics, Metagenomics and RNA-seq

Paul W. Bible, Lisa Federer, Allissa Dillman, 2015, bioRxiv.

Cell type and condition specific functional annotation of schizophrenia associated non-coding genetic variants

M. Rossner, Laura T. Jiménez-Barrón, C. Rummel, 2023, bioRxiv.

Distinct genetic liability profiles define clinically relevant patient strata across common diseases

T. Schulze, H. Völzke, J. Gagneur, 2023, medRxiv.