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The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome

research The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome

7 citations , January 2015 in “Case reports in genetics”

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

research The Association of Gene Expression and Single Nucleotide Polymorphism (rs 6152 SNP) in Androgen Receptor Gene with Recurrent Spontaneous Abortion (RSA) in Iraqi Women

March 2021 in “Medico-Legal Update”

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

research Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men

78 citations , August 2012 in “Human molecular genetics online/Human molecular genetics”

A new gene, JMJD1C, may affect testosterone levels in men.

research Efficacy and Safety of Ritlecitinib in the Asian Subpopulation of the ALLEGRO ‐2b/3 and ALLEGRO ‐ LT Clinical Studies for Alopecia Areata

February 2026 in “The Journal of Dermatology”

Ritlecitinib effectively regrows scalp, eyebrow, and eyelash hair in Asians with alopecia areata and is safe.

research Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia

3 citations , September 2019 in “PLOS ONE”

Genetic variations affect dutasteride treatment response for male pattern hair loss.

research Novel missense mutation in the EDA gene in a family affected by oligodontia

12 citations , January 2016 in “Journal of Orofacial Orthopedics / Fortschritte der Kieferorthopädie”

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

research ISID1343 - Efficacy of asymmetric siRNA targeting androgen receptor for the treatment of androgenetic alopecia

May 2023

The conclusion is that a treatment called cp-asiAR can reduce hair loss and promote hair growth, making it a potential new therapy for androgenetic alopecia.

research Newly formed Asian Association of Hair Restoration Surgeons (AAHRS)

July 2010 in “Hair transplant forum international”

A new group called the Asian Association of Hair Restoration Surgeons (AAHRS) has been created.

research Androgenetic Alopecia

1 citations , January 2018 in “Jaypee Brothers Medical Publishers (P) Ltd. eBooks”

research Androgenetic Alopecia

January 2018 in “Jaypee Brothers Medical Publishers (P) Ltd. eBooks”

research Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma

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.

research Androgenetic Alopecia

July 1996 in “Hair transplant forum international”

research Strontium Ranelate Promotes Chondrogenesis Through Inhibition of the Wnt/β-catenin Pathway

March 2021 in “Research Square (Research Square)”

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.

research Dermatology for the Non-Dermatologist: Triangular Alopecia

2 citations , November 1999 in “Hair transplant forum international”

The document's conclusion cannot be provided because the document is not accessible.

Immune Deficiency-Related Enteropathy-Lymphocytopenia-Alopecia Syndrome Results from Tetratricopeptide Repeat Domain 7A Deficiency

research Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency

64 citations , August 2014 in “The journal of allergy and clinical immunology/Journal of allergy and clinical immunology/The journal of allergy and clinical immunology”

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

research CCDC22 and CCDC93, two potential retriever-interacting proteins, are required for root and root hair growth in Arabidopsis

December 2022 in “Frontiers in plant science”

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

research Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis

August 2019 in “Anais Brasileiros de Dermatologia”

research The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle

51 citations , January 2007 in “Animal Genetics”

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

research GJB6 missense variant in a Labrador Retriever with paw pad hyperkeratosis

January 2026 in “Animal Genetics”

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

research CS12192 Reverses Alopecia Areata by Selectively Targeting JAK3/JAK1/TBK1.

February 2025 in “PubMed”

CS12192 effectively treats alopecia areata with better safety than current options.

research A Proposal from Steven C. Chang, MD

November 2001 in “Hair transplant forum international”

The document's conclusion cannot be provided because the document is not readable.

research Fellow of the ISHRS (FISHRS)

November 2014 in “International Society of Hair Restoration Surgery”

Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets (HVDRR): Clinical Heterogeneity and Long-Term Efficacious Management of Eight Patients from Four Unrelated Arab Families with a Loss of Function VDR Mutation

research Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation

6 citations , June 2018 in “Journal of pediatric endocrinology & metabolism/Journal of pediatric endocrinology and metabolism”

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.