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Publications in Genetics

Association of Parkinson Disease With Structural and Regulatory Variants in the HLA Region

American Journal of Human Genetics

English

Large-Scale Trans -eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-Regulation

American Journal of Human Genetics

English

Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated With Childhood-Onset, Slowly Progressive Nemaline Myopathy

American Journal of Human Genetics

English

Vertebrate Neural Stem Cell Segmentation, Tracking and Lineaging With Validation and Editing

Nature Protocols

Molecular Biology

English

Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome

American Journal of Human Genetics

English

Extinction of Conditioned Opiate Withdrawal in Rats in a Two-Chambered Place Conditioning Apparatus

Nature Protocols

Molecular Biology

English

Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes

American Journal of Human Genetics

English

Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy

American Journal of Human Genetics

English

Craniosynostosis and Multiple Skeletal Anomalies in Humans and Zebrafish Result From a Defect in the Localized Degradation of Retinoic Acid

American Journal of Human Genetics

English

Whole-Genome Chromatin Profiling From Limited Numbers of Cells Using Nano-ChIP-Seq

Nature Protocols

Molecular Biology

English