Author

Jayarama Shanker Kadandale

Observed names: J.S. Kadandale, Jayarama Kadandale, Jayarama S Kadandale, Jayarama S. Kadandale, Kadandale, J.S.

Observed institutions: Nitte University, University of Tennessee Health Science Center, Shamnur Shivashankarappa Institute of Medical Sciences & Research Centre, Centre For Human Genetics, Biotech Park, Sri Siddhartha Medical College, K S Hegde Medical Academy, University of Tennessee at Knoxville

ORCID: 0000-0002-1718-1544

Observed ORCID: 0000-0002-1718-1544

OpenAlex ID: A5013453398

Next-Generation Sequencing Reveals Novel Mutations in X-linked Intellectual Disability

2017 · Babylakshmi Muthusamy, Lakshmi Dhevi N. Selvan, et al. · OMICS A Journal of Integrative Biology · 44

Localization of SRY by primed in situ labeling in XX and XY sex reversal

2000 · Jayarama S. Kadandale, Stephen S. Wachtel, et al. · American Journal of Medical Genetics · 37

Long-term survival in Patau syndrome

2001 · Yusuf Tunca, Jayarama S. Kadandale, et al. · Clinical Dysmorphology · 35

Characterization of TTAGG telomeric repeats, their interstitial occurrence and constitutively active telomerase in the mealybug Planococcus lilacinus (Homoptera; Coccoidea)

2010 · Kommu Naga Mohan, B. Sandya Rani, et al. · Chromosoma · 26

Hypomelanosis of Ito and a ‘mirror image’ whole chromosome duplication resulting in trisomy 14 mosaicism

2000 · Yusuf Tunca, R.Sid Wilroy, et al. · Annales de Génétique · 26

Chromosomal Localization of Single Copy Genes SRY and SOX3 by Primed In Situ Labeling (PRINS)

2000 · Jayarama S. Kadandale, Yusuf Tunca, et al. · Microbial & Comparative Genomics · 24

Deletion of RBM and DAZ in azoospermia: Evaluation by PRINS

2001 · Jayarama S. Kadandale, Stephen S. Wachtel, et al. · American Journal of Medical Genetics · 22

Preimplantation Genetic Testing for Couples with Balanced Chromosomal Rearrangements

2022 · Sachin Shetty, Jiny Nair, et al. · Journal of Reproduction & Infertility · 18

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Y chromosome microdeletion and cytogenetic findings in male infertility: A cross-sectional descriptive study

2021 · Meenakshi Arumugam, Deyyanthody Prashanth Shetty, et al. · International Journal of Reproductive BioMedicine (IJRM) · 18

Primed in situ labeling (PRINS) for evaluation of gene deletions in cancer

2001 · Sugandhi A. Tharapel, Jayarama S. Kadandale · American Journal of Medical Genetics · 18

Clinical and Molecular Characterization of Prader-Willi Syndrome

2017 · G. N. Sanjeeva, Madhuri Maganthi, et al. · The Indian Journal of Pediatrics · 17

Prader Willi/Angelman and DiGeorge/velocardiofacial syndrome deletions: Diagnosis by primed in situ labeling (PRINS)

2001 · Avirachan T. Tharapel, Jayarama S. Kadandale, et al. · American Journal of Medical Genetics · 15

Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report

2015 · Aswini Sivasankaran, Ambika Srikanth, et al. · Molecular Syndromology · 11

Splice, Insertion‐Deletion and Nonsense Mutations that Perturb the Phenylalanine Hydroxylase Transcript Cause Phenylketonuria in India

2013 · Murali D. Bashyam, Ajay K. Chaudhary, et al. · Journal of Cellular Biochemistry · 9

Cytogenetic, epidemiological and clinical profile of children with Down syndrome in Karnataka

2018 · Krishnaveni Sharath, Asha K.R., et al. · Journal of Anatomical Society of India · 6

Consanguinity and Chromosomal Abnormalities

2017 · Lakshmi Prabha Subhash R, Anupama D, et al. · International Journal of Anatomy and Research · 5

Risk factors in childhood stunting in Karnataka, India, vary by geography

2021 · Srilakshmi M. Raj, Ruwanthi Ekanayake, et al. · Current Science · 3

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Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers

2016 · Mitesh Shetty, Ambika Srikanth, et al. · Cytogenetic and Genome Research · 3

Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum

2015 · Mitesh Shetty, Ambika Srikanth, et al. · Molecular Syndromology · 3

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Variation at Diabetes- and Obesity-Associated Loci May Mirror Neutral Patterns of Human Population Diversity and Diabetes Prevalence in India

2013 · Srilakshmi M. Raj, Pradeep Halebeedu, et al. · Annals of Human Genetics · 3

Mixed Gonadal Dysgenesis with 45,X/46,X,idic(Y)/46,XY Karyotype: A Case Report

2024 · Reshma Ammu Shetty, Deyyanthody Prashanth Shetty, et al. · Journal of Reproduction & Infertility · 2

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The Chromosomes of Dictyostelium Giganteum

2024 · Rishikesh Kumar, Pooja S. Kulshreshtha, et al. · 2

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Localization of the SRY Gene on Chromosome 3 in a Patient with Azoospermia and a Complex Karyotype 45,X/46,X,i(Y)(q10)/46,XX/ 47,XX,i(Y)(q10)

2018 · Linda C. Barnabas, Anbu Sumathy, et al. · Cytogenetic and Genome Research · 2

Practice of Consanguinity and Unusual Cases of Inherited Familial Chromosome Abnormalities: A Case Report.

2016 · Debarshi Sanyal, Vidya Bhairi, et al. · PubMed Central · 2

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Female Patient With a Variant of Turner Syndrome

2014 · Meenakshi A., Prashanth Shetty, et al. · Journal of Health and Allied Sciences NU · 2

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Works count: 43

Citation count: 359

H-index: 12

I10-index: 13