C. Srisailapathy

发表

Risk assessment of rail haulage accidents in inclined tunnels with Bayesian network and bow-tie model

Justin Margret Jeffrey, J. Chandru, Amritkumar Pavithra, 2018 .

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.

P. Coucke, C. Srisailapathy, G. Van Camp, 1995, Human molecular genetics.

A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus.

A. Lalwani, C. Srisailapathy, S. Kumar, 1995, Human molecular genetics.

Rare compound heterozygosity involving dominant and recessive mutations of GJB2 gene in an assortative mating hearing impaired Indian family

Justin Margret Jeffrey, J. Chandru, Amritkumar Pavithra, 2016, European Archives of Oto-Rhino-Laryngology.

Audiometric notch as a sign of noise induced hearing loss (NIHL) among the rice and market flour mill workers in Tamil Nadu, South India

R. Rajagopalan, C. Srisailapathy, Sharanya Narasimhan, 2022 .

Genetic analysis of SLC26A4 gene (pendrin) related deafness among a cohort of assortative mating families from southern India

Justin Margret Jeffrey, J. Chandru, C. Srisailapathy, 2020, European Archives of Oto-Rhino-Laryngology.

FMR1 gene CGG repeat distribution among the three individual cohorts with intellectual disability, autism, and primary ovarian insufficiency from Tamil Nadu, Southern India

S. Chong, C. Srisailapathy, Jeffrey Justin Margret, 2021, Advanced genetics.

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

K. Elbedour, R. Carmi, C. Srisailapathy, 1998, Human mutation.

Immune-mediated Sensorineural Hearing Loss: Patho-Mechanisms and Therapeutic Strategies

K. Ramkumar, C. Srisailapathy, S. ParidhyVanniya., 2019, Turkish Journal of Immunology.

Localization of a gene for otosclerosis to chromosome 15q25-q26.

P. Willems, P. Coucke, C. Srisailapathy, 1998, Human molecular genetics.

Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE

C. Srisailapathy, A. Anand, Arunima Chatterjee, 2014, PloS one.

PNPT1, MYO15A, PTPRQ, and SLC12A2‐associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India

N. Shomron, K. Avraham, Justin Margret Jeffrey, 2021, Annals of human genetics.

Genetic and phenotypic heterogeneity in PNPT1, MYO15A, PTPRQ and SLC12A2 variants detected among hearing impaired assortative mating families in Southern India

N. Shomron, K. Avraham, Justin Margret Jeffrey, 2021, bioRxiv.

New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p.

V. Sheffield, M. Lovett, C. Srisailapathy, 1997, American journal of medical genetics.

Evaluation of recurrent GNPTAB, GNPTG, and NAGPA variants associated with stuttering

C. Srisailapathy, Jeffrey Justin Margret, Chandru Jayasankaran, 2020, Advanced genetics.

Passage to India: The Search for Genes Causing Autosomal Recessive Nonsyndromic Hearing Loss

C. Srisailapathy, A. Ramesh, K. Fukushima, 1998, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human

J. R. Holt, H. Kremer, C. Srisailapathy, 2011, Nature communications.

Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss

Shelly Chadha, Aparna Ganapathy, R. Mani, 2009, European Journal of Human Genetics.

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.

Shelley D. Smith, P. Coucke, C. Srisailapathy, 1995, Genome research.

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.

M. Lovett, P. Coucke, C. Srisailapathy, 1998, American journal of medical genetics.

Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals

C. Srisailapathy, M. Subathra, A. Ramesh, 2016, Annals of human genetics.

Low incidence of GIPC3 variants among the prelingual hearing impaired from southern India

Justin Margret Jeffrey, J. Chandru, M. Kalaimathi, 2020, Journal of genetics.

Is Screening for Mitochondrial A1555G Mutation among Assortative Mating Hearing Impaired Families Important? : A Prefatory Quest

J. Chandru, C. Srisailapathy, M. Subathra, 2014 .

Refining the DFNB17 interval in consanguineous Indian families

D. Choo, V. Pilipenko, C. Srisailapathy, 2004, Molecular Biology Reports.

Autosomal Dominant Hearing Loss resulting from p.R75Q Mutation in the GJB2 Gene: Nonsyndromic presentation in a South Indian Family

C. Srisailapathy, Murali Narasimhan, A. Pavithra, 2015, Annals of human genetics.

Exclusion of Putative CATSPER2 and STRC Gene Deletion and FOXI1 Gene Mutations in a Unique Cohort with Sensorineural Deafness and Male Infertility from South India

Justin Margret Jeffrey, J. Chandru, M. Kalaimathi, 2018, Current Science.

Low incidence of GIPC3 variants among the prelingual hearing impaired from southern India

Justin Margret Jeffrey, J. Chandru, M. Kalaimathi, 2020, Journal of Genetics.

Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.

V. Sheffield, M. Lovett, C. Morton, 1997, Genome research.

Unraveling the Genetic Basis of Combined Deafness and Male Infertility Phenotypes through High‐Throughput Sequencing in a Unique Cohort from South India

C. Srisailapathy, H. Azaiez, Jeffrey Justin Margret, 2024, Advanced genetics.

Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2.

B J Keats, V. Sheffield, R. Swiderski, 2000, Gene.