James T. Bennett

Seattle Children's Hospital — United States

Medicine · Health Sciences

40h-index5.7kcitations171works3.42yr avg
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Research Topics

Scoliosis diagnosis and treatment(28), Spinal Fractures and Fixation Techniques(25), Genomics and Rare Diseases(21), Vascular Malformations and Hemangiomas(18), Hip disorders and treatments(17)

Publications170 total

Implementation of First‐Line Rapid Genome Sequencing for Children in Pediatric and Cardiac Intensive Care Units
American Journal of Medical Genetics Part A·2026Open Access
Mapping single-cell diploid chromatin fiber architectures using DAF-seq
Nature Biotechnology·2025· 1 cited
Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data
2025· 1 citedOpen Access
A telomere-to-telomere map of somatic mutation burden and functional impact in cancer
2025· 2 citedOpen Access
Isolated lateralized overgrowth and the need for tumor screening: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2025Open Access
The Somatic Mosaicism across Human Tissues Network
Nature·2025· 28 citedOpen Access
Implementation of First-Line Rapid Genome Sequencing in Non–Critical Care Pediatric Wards
The Journal of Pediatrics·2025· 1 citedOpen Access
Mosaic X-linked adrenoleukodystrophy in males identified by newborn screening and next-generation sequencing
npj Genomic Medicine·2025Open Access
Non-coding cis-regulatory variants in HK1 cause congenital hyperinsulinism with variable disease severity
Genome Medicine·2025· 7 citedOpen Access
44: Capillary Malformation-Arteriovenous Malformation Syndrome: Proposed Consensus Guidelines
Journal of Investigative Dermatology·2025
Large copy number variants are an important cause of congenital hyperinsulinism that should be screened for during routine testing
Frontiers in Endocrinology·2025· 1 citedOpen Access
Low rate of healing and high incidence of complications in benign pediatric bone tumors treated with synthetic calcium sulfate–calcium phosphate bone graft
Journal of Children s Orthopaedics·2025· 1 citedOpen Access
Bipolar sternocleidomastoid partial resection in pediatric patients case report: Technique and early outcomes
Medicine·2024Open Access
The p.( <scp>Gly111Arg</scp> ) <i>ABCC8</i> Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community
Clinical Genetics·2024Open Access
Author response for "The p.(&lt;scp&gt;Gly111Arg&lt;/scp&gt;) &lt;i&gt;ABCC8&lt;/i&gt; Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community"
2024
Deaminase-assisted single-molecule and single-cell chromatin fiber sequencing
2024· 8 citedOpen Access
Even Simpler Tone Curves
London Imaging Meeting·2024Open Access
A haplotype-resolved view of human gene regulation
2024· 24 citedOpen Access
P193: Inpatient genetics consults for nondysmorphic children: Characteristics, testing patterns and diagnostic yield
Genetics in Medicine Open·2024Open Access
Partial Removal of Spinal Implants for Pain After Posterior Spinal Fusion for Adolescent Idiopathic Scoliosis
JBJS Journal of Orthopaedics for Physician Assistants·2024
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Frequent Co-authors

Amer F. Samdani(9), William B. Dobyns(8), Joshua M. Pahys(7), Dana M. Jensen(6), Firoz Miyanji(6), Peter O. Newton(6), Randal R. Betz(6), Michael J. Bamshad(5), Andrew E. Timms(5), Patrick J. Cahill(5), Baron S. Lonner(5), Jonathan A. Perkins(4), Heather C. Mefford(4), Alexander F. Schier(4), Ghayda Mirzaa(4), Robin L. Bennett(3), Tom Walsh(3), Deborah A. Nickerson(3), Leslie G. Biesecker(3), Giridhar M. Shivaram(3)