D. Babcock

Most-cited papers

1. Mechanical Property Characterization of Electrospun Recombinant Human Tropoelastin for Vascular Graft Biomaterials

   K. A. McKenna, M. Hinds, R. Sarao, Ping-Cheng Wu +4 more

   2011Acta Biomaterialia148 citations Open access

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2. CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome

   C. Maslen, D. Babcock, S. Robinson, Lora J. H. Bean +3 more

   2006American Journal of Medical Genetics. Part A98 citations

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3. A rare branch-point mutation is associated with missplicing of fibrillin-2 in a large family with congenital contractural arachnodactyly.

   C. Maslen, D. Babcock, M. Raghunath, B. Steinmann

   1997American Journal of Human Genetics81 citations Open access

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4. T-cell receptor variable β genes show differential expression in CD4 and CD8 T cells

   M. Davey, M. M. Meyer, D. Munkirs, D. Babcock +3 more

   199154 citations

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5. A single mutation that results in an Asp to His substitution and partial exon skipping in a family with congenital contractural arachnodactyly

   D. Babcock, C. Gasner, U. Francke, C. Maslen

   1998Human Genetics34 citations

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6. CRELD2: gene mapping, alternate splicing, and comparative genomic identification of the promoter region.

   C. Maslen, D. Babcock, Jennifer K Redig, Katannya Kapeli +2 more

   2006Gene23 citations

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7. Sensitivity to targeted therapy differs between HER2-amplified breast cancer cells harboring kinase and helical domain mutations in PIK3CA

   J. Garay, Rebecca Smith, Kaylyn L. Devlin, D. Hollern +13 more

   2021Breast Cancer Research17 citations Open access

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8. Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects

   Jennifer K Redig, G. Fouad, D. Babcock, Benjamin Reshey +3 more

   2014AIMS Genetics16 citations Open access

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9. Prenatal ultrasound findings in a fetus with congenital contractural arachnodactyly

   N. Kölble, J. Wisser, D. Babcock, C. Maslen +2 more

   2002Ultrasound in Obstetrics and Gynecology16 citations

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10. Occurrence of a mutation associated with Wolman disease in a family with cholesteryl ester storage disease

    C. Maslen, D. Babcock, D. Illingworth

    1995Journal of Inherited Metabolic Disease7 citations

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11. T-cell receptor variable beta genes show differential expression in CD4 and CD8 T cells.

    M. Davey, M. M. Meyer, D. Munkirs, D. Babcock +3 more

    1991Human Immunology6 citations

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12. A free-radical design featuring an intramolecular migration for a synthetically versatile alkyl–(hetero)arylation of simple olefins

    D. Babcock, Andrew J. Wolfram, Jaxon L Barney, Santino M. Servagno +2 more

    2024Chemical Science0 citations Open access

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13. Mutation Analysis of Fibrillin-2 (FBN2) and Microfibril Associated Protein-3 (MFAP-3): Two Genes Associated with Congenital Contractural Arachnodactyly (CCA), also known as Beal's Syndrome

    D. Babcock

    20000 citations Open access

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14. Aberrant splicing of fibrillin-2 in a family with congenital contractual arachnodactyly

    C. Maslen, D. Babcock, M. Raghunath, B. Steinmann

    19970 citations

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15. Missense and splice-site mutations in a family with cholesterol ester storage disease

    C. Maslen, D. Babcock, D. Illingworth

    19940 citations

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