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    1. A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters 2012
    2. X linked mental retardation. Journal of Medical Genetics · 1991 · 79 citations
    3. Commonly associated disorders with complete scalp alopecia in early childhood: A review International journal of trichology · 2023
    4. Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods” Canadian journal of neurological sciences · 2021 · 1 citations
    5. <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients Clinical genetics · 2010 · 43 citations
    6. Woodhouse-Sakati Syndrome: The New Genetic Variant of DCAF17 In 2 Adult Sisters JCEM Case Reports · 2024 · 1 citations
    7. Gomez–Lopez-Hernandez Syndrome: Two New Cases and Review of the Literature Pediatric neurology · 2008 · 23 citations
    8. Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome Clinical and Experimental Ophthalmology · 2004 · 6 citations
    9. Poster Presentations International Journal of Trichology · 2012
    10. Telogen hair loss and androgenetic‐like alopecia in GAPO syndrome Australasian Journal of Dermatology · 2018 · 1 citations
    11. Disorders of hair Journal of the American Academy of Dermatology · 1988 · 6 citations
    12. Rapunzel Syndrome as a Rare Presentation of Trichobezoar ˜The œInternet journal of surgery · 2008
    13. Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes ˜The œAmerican journal of pathology · 2010 · 35 citations
    14. Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure Journal of the American Academy of Dermatology · 1984 · 30 citations
    15. Bloom's syndrome–‐a first report from India International Journal of Dermatology · 2000 · 13 citations
    16. The Role of Zinc in Gastrointestinal and Liver Disease Clinics in Gastroenterology · 1983 · 82 citations
    17. Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome Journal of Plastic Surgery and Hand Surgery · 2013 · 4 citations
    18. A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia Archives of Dermatological Research · 2015 · 2 citations
    19. Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity Journal of Rare Diseases · 2024
    20. Common Dermatologic Disorders in Down Syndrome: Systematic Review JMIR Dermatology · 2022 · 10 citations
    21. Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings Scholars Journal of Medical Case Reports · 2021
    22. Screening guidelines for thyroid function in children with alopecia areata Journal of The American Academy of Dermatology · 2018
    23. Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide Cureus · 2026
    24. Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss Cell Stem Cell · 2007 · 688 citations
    25. Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern Journal der Deutschen Dermatologischen Gesellschaft · 2004 · 30 citations
    26. Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome Orphanet Journal of Rare Diseases · 2011 · 71 citations
    27. Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report Clinical Cosmetic and Investigational Dermatology · 2023
    28. Congenital atrichia and hypotrichosis World Journal of Pediatrics · 2011 · 11 citations
    29. HAIR AND SYSTEMATIC DISEASE Dermatologic Clinics · 2001 · 58 citations
    30. Hair Loss in Children Current problems in dermatology · 2015 · 24 citations