Suzanne M Leal

25PUBLICATIONS
75CO-AUTHORS
Stochastic analysis and modellingGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)GenomicsNeurogenetics
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Publications (25)

|Jul 17, 2026
LDSC regression-based heritability estimates can be biased when summary statistics are obtained from meta-analysis or imputed variants.

|Jun 05, 2026
Leveraging cis- and trans- variants to improve protein expression level prediction for proteome-wide association studies.

|Mar 07, 2025
Mendelian non-syndromic and syndromic hearing loss genes contribute to presbycusis.

Diana M Cornejo-Sanchez, Thashi Bharadwaj, Rui Dong

|Feb 12, 2025
Whole Genome Sequencing of Pedigrees With High Density of Substance Use and Psychiatric Disorders: A Meeting Report.

Shirley Y Hill, Howard J Edenberg, Aiden Corvin

|Dec 19, 2024
THBS1 is a new autosomal recessive non-syndromic hearing impairment gene.

Thashi Bharadwaj, Anushree Acharya, Fati Ullah Khan

|Oct 11, 2023
A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndrome.

Madiha Amin Malik, Muhammad Arif Nadeem Saqib, Edwin Mientjes

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Frequent Collaborators

6 joint publications

Isabelle Schrauwen

5 joint publications

Thashi Bharadwaj

5 joint publications

Khurram Liaqat

3 joint publications

Abdul Nasir