Sungkook Hong

Most-cited papers

1. An Ultraconserved Brain-specific Enhancer within ADGRL3 (LPHN3) Underpins ADHD Susceptibility

   Ariel F. Martinez, Yu Abe, Sungkook Hong, K. Molyneux +6 more

   2016Biological Psychiatry67 citations Open access

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2. Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome.

   Sungkook Hong, P. Hu, J. Marino, Sophia B. Hufnagel +7 more

   2016Human Molecular Genetics51 citations Open access

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3. Phenotype Delineation of ZNF462 related syndrome

   P. Kruszka, Tommy Hu, Sungkook Hong, R. Signer +28 more

   2019American Journal of Medical Genetics. Part A38 citations Open access

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4. A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly.

   P. Kruszka, Seth I. Berger, K. Weiss, Joshua L. Everson +5 more

   2019American Journal of Human Genetics37 citations Open access

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5. Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF‐β, hedgehog, and FGF signaling

   E. Roessler, P. Hu, J. Marino, Sungkook Hong +14 more

   2018Human Mutation25 citations Open access

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6. Limb body wall complex, amniotic band sequence, or new syndrome caused by mutation in IQ Motif containing K (IQCK)?

   P. Kruszka, A. Uwineza, L. Mutesa, Ariel F. Martinez +10 more

   2015Molecular Genetics & Genomic Medicine24 citations Open access

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7. Loss-of-function mutations in FGF8 can be independent risk factors for holoprosencephaly

   Sungkook Hong, P. Hu, E. Roessler, Tommy Hu +1 more

   2018Human Molecular Genetics18 citations Open access

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8. Functional analysis of Sonic Hedgehog variants associated with holoprosencephaly in humans using a CRISPR/Cas9 zebrafish model

   Sungkook Hong, P. Hu, J. Jang, B. Carrington +4 more

   2020Human Mutation10 citations Open access

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9. Unique Alterations of an Ultraconserved Non-Coding Element in the 3′UTR of ZIC2 in Holoprosencephaly

   E. Roessler, P. Hu, Sungkook Hong, Kshitij Srivastava +9 more

   2012PLoS ONE9 citations Open access

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10. Rare hypomorphic human variation in the heptahelical domain of SMO contributes to holoprosencephaly phenotypes

    M. Nagai-Tanima, Sungkook Hong, P. Hu, B. Carrington +3 more

    2020Human Mutation4 citations Open access

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11. Rare hypomorphic human variation in the heptahelical domain of SMOOTHENED contributes to holoprosencephaly phenotypes

    M. Nagai-Tanima, Sungkook Hong, P. Hu, B. Carrington +3 more

    20201 citations Open access

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12. Cover, Volume 41, Issue 12

    M. Nagai-Tanima, Sungkook Hong, P. Hu, B. Carrington +3 more

    20200 citations Open access

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13. Abstracts of the 17th Biennial Congress of the Southern African Society for Human Genetics Conference organiser

    M. Muenke, B. Solomon, D. Hadley, R. Hart +5 more

    20170 citations

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