Andrew J. Sharp

Child Health and Development Institute — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

52h-index13.5kcitations216works7.82yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genomic variations and chromosomal abnormalities(50), Epigenetics and DNA Methylation(42), Genetic Syndromes and Imprinting(31), Chromosomal and Genetic Variations(28), Genetics and Neurodevelopmental Disorders(25)

Publications215 total

Evidence-Based Medicine and Medical Informatics
2025
A phenome-wide association study of CNVs genotyped from genome sequencing read depth in the UK Biobank
2025Open Access
Using interpretable rule-learning artificial intelligence to optimally differentiate adrenal pheochromocytomas from adenomas with CT radiomics
Abdominal Radiology·2025
A Population‐Wide Exploration of the <scp><i>THAP11</i> CAG</scp> Repeat Size and Structure in the 100,000 Genomes Project and <scp>UK</scp> Biobank
Movement Disorders·2024· 2 citedOpen Access
A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank
Nature Communications·2024· 9 citedOpen Access
Genetic variation of tandem repeats as a cause of Alzheimer’s Disease
Alzheimer s & Dementia·2024Open Access
Increased frequency of repeat expansion mutations across different populations
Nature Medicine·2024· 54 citedOpen Access
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disability
Nature Genetics·2024· 9 citedOpen Access
G008 Population analysis of repeat expansions indicates increased frequency of pathogenic alleles across different populations
2024· 1 citedOpen Access
TRGT-denovo: accurate detection of <i>de novo</i> tandem repeat mutations
2024· 5 citedOpen Access
A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank
2024· 6 citedOpen Access
Feeder-free generation and characterization of endocardial and cardiac valve cells from human pluripotent stem cells
iScience·2023· 12 citedOpen Access
Daylight photodynamic therapy as a treatment for actinic field change in patients diagnosed with oculocutaneous albinism in sub-Saharan Africa
Clinical and Experimental Dermatology·2023
Increased frequency of repeat expansion mutations across different populations
2023· 13 citedOpen Access
Population Frequency of Repeat Expansions Indicates Increased Disease Prevalence Estimates Across Different Populations
Research Square (Research Square)·2023· 2 citedOpen Access
Compact High Power Density Axial Flux PM Motor for Surgical Robotics Application
2023
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disability
2023· 7 citedOpen Access
Small open reading frames: a comparative genetics approach to validation
BMC Genomics·2023· 9 citedOpen Access
Low iodine knowledge in a group of Chinese breastfeeding women with adequate iodine status
2023
Feeder-Free Generation of Endocardial and Cardiac Valve Cells from Human Pluripotent Stem Cells
2023Open Access
page 1 of 11Next →

Frequent Co-authors

Evan E. Eichler(13), Paras Garg(10), Corey T. Watson(9), Heather C. Mefford(7), Samantha J.L. Knight(7), Regina Regan(5), Stylianos E. Antonarakis(5), Tomàs Marquès‐Bonet(5), Donna G. Albertson(4), Daniel Pinkel(4), Ze Cheng(4), Stuart Schwartz(4), Carl Baker(4), Raoul C. M. Hennekam(4), Marco Fichera(4), Giorgio Gimelli(4), Corrado Romano(4), Charles E. Schwartz(4), Bert B.A. de Vries(4), Helen Stewart(4)