David H Ledbetter

12PUBLICATIONS
99CO-AUTHORS
Developmental genetics (incl. sex determination)Sequence analysisEpigenetics (incl. genome methylation and epigenomics)Cancer diagnosisGene expression (incl. microarray and other genome-wide approaches)
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Publications (12)

|Oct 15, 2024
A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk.

Alexander S F Berry, Brenda M Finucane, Scott M Myers

|Oct 22, 2020
Exome sequencing and characterization of 49,960 individuals in the UK Biobank.

Cristopher V Van Hout, Ioanna Tachmazidou, Joshua D Backman

|Jul 31, 2020
Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.

Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies

|Apr 30, 2020
Feasibility of blood testing combined with PET-CT to screen for cancer and guide intervention.

Anne Marie Lennon, Adam H Buchanan, Isaac Kinde

|Oct 27, 2019
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders.

M T Oetjens, M A Kelly, A C Sturm

|Sep 25, 2019
A framework for the investigation of rare genetic disorders in neuropsychiatry.

Stephan J Sanders, Mustafa Sahin, Joseph Hostyk

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