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research The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study

15 citations , December 2017 in “Journal of Investigative Dermatology”

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Association of Psoriasis and Psoriatic Arthritis with Human Leukocyte Antigen and Killer Cell Immunoglobulin-Like Receptor Gene Frequency: A Multiethnic Population Study

research Association of psoriasis and psoriatic arthritis with human leukocyte antigen and killer cell immunoglobulin–like receptor gene frequency: A multiethnic population study

February 2009 in “Journal of The American Academy of Dermatology”

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

research Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases

January 2012 in “Faculty of Health; Institute of Health and Biomedical Innovation”

Early-onset hair loss is linked to Parkinson's disease and decreased fertility.

research Association between VEGF gene polymorphisms (11 sites) and polycystic ovary syndrome risk

5 citations , January 2020 in “Bioscience Reports”

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

research A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females

103 citations , March 2015 in “Nature Communications”

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Faculty Opinions Recommendation of Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases

research Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.

October 2012 in “Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature”

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

research Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases

26 citations , May 2024 in “Molecular Neurodegeneration”

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

research Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous

5 citations , May 2022 in “Diagnostics”

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

research Finding bald spots on chromosome 20p11

1 citations , February 2009 in “Clinical Genetics”

New genes linked to male pattern baldness were found on chromosome 20p11.

research DYS459, DYS391, DYS388 and DYS19 genetic loci have high allelic frequency in patients with prostate cancer

August 2015 in “International Journal of Genetics and Molecular Biology”

Certain genetic markers may increase or decrease prostate cancer risk.

research Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.

October 2012 in “Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature”

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

research Genetics of Diabetes in Childhood

January 2003 in “Springer eBooks”

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

research Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease

12 citations , February 2021 in “Translational Psychiatry”

Researchers found two new genetic variants linked to Alzheimer's disease.

research Common variants in the sex hormone-binding globulin gene (SHBG) and polycystic ovary syndrome (PCOS) in Mediterranean women

39 citations , September 2012 in “Human Reproduction”

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

research Exome-wide age-of-onset analysis reveals exonic variants in ERN1, TACR3 and SPPL2C associated with Alzheimer’s disease

January 2020 in “bioRxiv (Cold Spring Harbor Laboratory)”

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

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 Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis

2 citations , February 2024 in “Medicine”

A mutation in the IL2RA gene increases the risk of alopecia areata.

research Polymorphisms in the promoter regions of the CXCL1 and CXCL2 genes contribute to increased risk of alopecia areata in the Korean population

8 citations , January 2015 in “Genetics and Molecular Research”

Certain gene variations increase the risk of alopecia areata in Koreans.

research INNOVATIVE APPROACH TO CRC PREVENTION: THE ROLE OF LOW-PENETRATION GENES

January 2024 in “Wiadomości Lekarskie”

Low-penetration genes might help personalize colorectal cancer prevention.

research Male-pattern baldness susceptibility locus at 20p11

111 citations , October 2008 in “Nature Genetics”

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

research Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing

October 2023 in “Psychiatry research. Case reports”

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

research A genome‐wide association study identified a genetic variant associated with hair thinning in Japanese women

March 2023 in “Journal of Cosmetic Dermatology”

A genetic variant linked to hair thinning in Japanese women was found.

research Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women

15 citations , January 2010 in “Reproduction, Fertility and Development”

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

research Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne

43 citations , November 2018 in “Nature Communications”

Genetic variations affecting skin structure play a key role in severe acne.

research Susceptibility variants for male-pattern baldness on chromosome 20p11

140 citations , October 2008 in “Nature Genetics”

Alopecia Areata Susceptibility Variant Identified by MHC Risk Haplotype Sequencing Reproduces Symptomatic Patched Hair Loss in Mice

research Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice

April 2018 in “bioRxiv (Cold Spring Harbor Laboratory)”

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Genotyping Of The Rs1800440 Polymorphism In CYP1B1 Gene And The Rs9258883 Polymorphism In HLA-B Gene In A Spanish Cohort Of 223 Patients With Frontal Fibrosing Alopecia

research Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia

1 citations , September 2023 in “Acta dermato-venereologica”

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

research Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.

June 2012 in “Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature”

Six new risk spots for early hair loss were found, which also link to Parkinson's disease and lower fertility. Two genes, FOXA2 and HDAC4, could be new treatment targets. Hair loss might also be connected to heart disease, metabolic syndrome, and prostate cancer.

research The genetic basis of dermatophytosis skin infection susceptibility

March 2026 in “Nature Communications”

Genetic factors, skin barrier, immune function, and obesity influence risk of fungal skin infections.

research Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

November 2020 in “UNC Libraries”

Seven new genetic risk areas for prostate cancer were found.

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