September 2019 in “The journal of investigative dermatology/Journal of investigative dermatology” A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.
1 citations
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September 2023 in “Journal of the American Academy of Dermatology” May 2024 in “Clinical and experimental optometry” 
7 citations
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January 2015 in “Dermatology” Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.
1 citations
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May 2024 in “Human Genomics” Polygenic risk scores can predict the risk and outcomes of benign prostatic hyperplasia.
1 citations
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September 2024 in “Journal of the American Academy of Dermatology” 
March 1997 in “Hair transplant forum international” The document's content couldn't be understood or processed.
January 2026 in “Biochemical Pharmacology” April 2014 in “Investigative Ophthalmology & Visual Science” 
1 citations
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September 2023 in “Journal of the American Academy of Dermatology” May 2020 in “The Journal of Urology” 
March 2011 in “European Urology Supplements” Gene variation affects prostate issues and hair loss.
7 citations
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February 2011 in “Journal of dermatology” The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.
July 2008 in “Hair transplant forum international” The document cannot be understood or processed.
November 1995 in “Hair transplant forum international” The document cannot be understood or processed.
September 2009 in “International Society of Hair Restoration Surgery” 
June 2019 in “Reactions Weekly” April 2011 in “Reactions Weekly” October 2024 in “Frontiers in Oncology” A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.
A rare case of hypotrichosis with juvenile macular dystrophy (HJMD) was identified in a six-year-old Saudi girl with sparse scalp hair and progressive vision loss. Born to consanguineous parents, she exhibited symptoms from birth, including decreased night vision and cone-rod dysfunction. Genetic analysis revealed a homozygous missense mutation, c.1918T>G (p.Cys640Gly), in the CDH3 gene. This finding contributes to the understanding of the genetic spectrum of HJMD in Saudi Arabia, highlighting the importance of genetic evaluation in patients with similar clinical features.
September 2023 in “Zenodo (CERN European Organization for Nuclear Research)” 3 citations
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January 2008 in “Drug Safety” 
April 2016 in “The Journal of Sexual Medicine” November 2014 in “International Society of Hair Restoration Surgery” 
August 2016 in “Journal of Investigative Dermatology” Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.
20 citations
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September 1987 in “The Lancet”