English

    Fellowship & Membership

  • Short-term Fellowship-Medical Genetics, York Hill Hospital, Glasgow, U.K.
  • European Board of Medical Genetics (EBMG).
  • Indian Society of Human Genetics (ISHG).
  • Indian Academy of Paediatrics-Genetics Specialty Chapter.
  • Bangalore Society of Obstetrics & Gynaecology.
  • Indian Society of Inborn Errors of Metabolism.
  • Indian Society of Prenatal Diagnosis & Therapy.
  • Molecular Pathology Association of India.

    • Field of Expertise

  • Two decades of extensive experience in the field of Medical Genetics Prenatal diagnosis & Genetic counseling
  • Genetic diagnosis of Down syndrome, Autism, β-Thalassemia, Haemophilia, Duchenne muscular dystrophy (DMD) & Spinal muscular atrophy (SMA) etc.
  • Genetic counseling in consanguinity, recurrent abortions, Infertility, Pre- implantation Genetic Screening Test (PGT), Non-Invasive Prenatal Screening (NIPT/NIPS)
  • Expertise in Karyotyping, FISH study, Double/Quadruple study, Chromosomal Microarray & Next Generation Sequencing (NGS)
  • Risk assessment in hereditary cancer disorders like Breast & Ovarian cancer

    • Languages Spoken

  • English
  • Hindi
  • Kannada
  • Tulu

    • Awards & Achievements

  • Faculty for a Certificate course in Genetic Counselling (MAHE).
  • Recognized Guide for Ph.D. in Manipal Academy of Higher Education (MAHE).
  • Guided Ph.D., M.Phil & MSc students & trained students for Genetic counseling.
  • Received IBM Sponsorship of CAS Project expenses towards clinical research.
  • Conducted a public awareness program on World Thalassemia Day (May 18) & World Down syndrome day (Mar 19).
  • Organized CME on “Integrating Genomics into Clinical Practice” (Jul 18) & “Autism awareness day” (Apr 19).
  • Published papers in National & International journals & CHAPTER IN BOOK-“Genetics in Congenital Heart Disease” In “A Comprehensive Approach to Congenital Heart Disease (A Lifelong Odyssey)” Jaypee brothers, ISBN 978-93-5090-267-7.

    • Talks & Publications

  • “Aneuploidy screening of sperm-is it useful? 26th Annual Conference organized by the Indian Society of Assisted Reproduction(ISAR)in Mumbai on 28th August.
  • “Genetic Counseling in Autism” organized by Manipal Advanced Centre for Child care on 17th April 2022.
  • “Genetic Testing to Shorten the Diagnostic Odyssey” organized by Manipal Advanced Centre for Child care on 13th April 2022.
  • “Down Syndrome Awareness Day 2022” organized by Rortact Club, Bangalore on 20th Mar 2022.
  • “IEM & Challenges in Prenatal Diagnosis” organized by NITTE University on 25th Feb 2022.
  • “Experience of chromosomal microarray applied in prenatal and postnatal settings “organized by Agilent India on 28th Jan 2022.
  • “Behind the scenes! Peek into the working of an NBS Lab” in the NATIONAL NEWBORN SCREENING SYMPOSIUM organized by the National Neonatal Forum India (NNFI) on 26th Sep 2021.
  • “Spinal Muscular Atrophy Awareness Discussion” Facebook Live organized by Integrated Health & Wellbeing (IHW) Council on 27th Aug 2021.
  • “Autism & Genomics” Organized by Lybrate GoodMD on 9th Mar 2021.
  • “Don’t Neglect Medical Genetics in Women’s Health” organized by the Obstetrics & Gynecology Society of Bangladesh on 10th Jan 2021.
  • "6th Edition of Year in Review Breast Cancer Conference" organized by Women’s Health Initiative by Tata Memorial Hospital, Mumbai held on 11th Jan 2021.
  • “Current status of Medical Genetics in India” Facebook Live organized by Cachar Chronicle on 18th Sep 20.
  • “Autism & Genomics” in Webinar on Insight into Autism & Fragile-X; organized by Indian Medical Association-Medical Student network in association with Fragile-X society, Indian on 22nd July 20.
  • “Our Experience of Chromosomal Microarray” in Celebrating 15 Years of Trusted Genomic Analysis with CGH on 26th Feb 20.
  • “Advanced Genetic Study with Interesting Case Scenarios” in Cloudnine-OAR Hospital on 11th Feb 20.
  • “Genetics in Clinical Practice” in Manipal Hospital, Goa on 8Th Jan 20.
  • “Genetic etiology of Developmental delay & disability” in CME on Developmental Pediatrics, SDUMC on 25th October 2019.
  • “Genetic disease Diagnosis & Gene therapy" in 41st CME in Internal Medicine organized by the Association of Physicians of India & Medical Education and Research Trust, Bangalore on 22th Sep 2019.
  • Panel discussion ‘CME on Anemia in Pregnancy; titled ‘The Pale Gravida’ - A Challenge !?!? on 22-Sep-2019, Bengaluru organized by The Society for Maternal-Fetal Medicine, (India).
  • A retrospective study of the profile and outcome of children with Dravet syndrome in a tertiary care hospital of Southern India, Journal of Pediatric Epilepsy (Accepted).
  • A novel mutation in GATA3 gene in a case of Hypoparathyroidism, Deafness and Renal dysplasia syndrome, Indian Journal of Nephrology (Accepted).
  • Sameeta M. Prabhu, Bidisha Banerjee, Ullas Acharya, Poonam P Hegde, Mitesh Shetty. MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes)—Usual and Unusual MRI Finding. Indian J Radiol Imaging https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0042-1755241.pdf.
  • Jyothsna Madan, Mitesh Shetty*, B S Ramamurthy, Surekha Managoli. “A Multidisciplinary approach for Prenatal diagnosis of FRASER SYNDROME - report of a novel variant in FRAS1.” Taiwanese Journal of Obstetrics and Gynecology, Volume 61(2022)129-132. https://doi.org/10.1016/j.tjog.2021.11.020.
  • Shetty M. “Genomics in infectious diseases” Pediatr Inf Dis 2021; 3 (2):57-64. https://www.pidjournal.com/doi/PID/pdf/10.5005/jp-journals-10081-1296.
  • Dr. Mitesh Shetty on More Bangaloreans take a genetic test to screen for future risk | Deccan Herald. Click Here

    Languages Spoken

  • English
  • Hindi
  • Kannada
  • Tulu

    • Fellowship & Membership

  • Short-term Fellowship-Medical Genetics, York Hill Hospital, Glasgow, U.K.
  • European Board of Medical Genetics (EBMG).
  • Indian Society of Human Genetics (ISHG).
  • Indian Academy of Paediatrics-Genetics Specialty Chapter.
  • Bangalore Society of Obstetrics & Gynaecology.
  • Indian Society of Inborn Errors of Metabolism.
  • Indian Society of Prenatal Diagnosis & Therapy.
  • Molecular Pathology Association of India.

    • Field of Expertise

  • Two decades of extensive experience in the field of Medical Genetics Prenatal diagnosis & Genetic counseling
  • Genetic diagnosis of Down syndrome, Autism, β-Thalassemia, Haemophilia, Duchenne muscular dystrophy (DMD) & Spinal muscular atrophy (SMA) etc.
  • Genetic counseling in consanguinity, recurrent abortions, Infertility, Pre- implantation Genetic Screening Test (PGT), Non-Invasive Prenatal Screening (NIPT/NIPS)
  • Expertise in Karyotyping, FISH study, Double/Quadruple study, Chromosomal Microarray & Next Generation Sequencing (NGS)
  • Risk assessment in hereditary cancer disorders like Breast & Ovarian cancer

    • Awards & Achievements

  • Faculty for a Certificate course in Genetic Counselling (MAHE).
  • Recognized Guide for Ph.D. in Manipal Academy of Higher Education (MAHE).
  • Guided Ph.D., M.Phil & MSc students & trained students for Genetic counseling.
  • Received IBM Sponsorship of CAS Project expenses towards clinical research.
  • Conducted a public awareness program on World Thalassemia Day (May 18) & World Down syndrome day (Mar 19).
  • Organized CME on “Integrating Genomics into Clinical Practice” (Jul 18) & “Autism awareness day” (Apr 19).
  • Published papers in National & International journals & CHAPTER IN BOOK-“Genetics in Congenital Heart Disease” In “A Comprehensive Approach to Congenital Heart Disease (A Lifelong Odyssey)” Jaypee brothers, ISBN 978-93-5090-267-7.

    • Talks & Publications

  • “Aneuploidy screening of sperm-is it useful? 26th Annual Conference organized by the Indian Society of Assisted Reproduction(ISAR)in Mumbai on 28th August.
  • “Genetic Counseling in Autism” organized by Manipal Advanced Centre for Child care on 17th April 2022.
  • “Genetic Testing to Shorten the Diagnostic Odyssey” organized by Manipal Advanced Centre for Child care on 13th April 2022.
  • “Down Syndrome Awareness Day 2022” organized by Rortact Club, Bangalore on 20th Mar 2022.
  • “IEM & Challenges in Prenatal Diagnosis” organized by NITTE University on 25th Feb 2022.
  • “Experience of chromosomal microarray applied in prenatal and postnatal settings “organized by Agilent India on 28th Jan 2022.
  • “Behind the scenes! Peek into the working of an NBS Lab” in the NATIONAL NEWBORN SCREENING SYMPOSIUM organized by the National Neonatal Forum India (NNFI) on 26th Sep 2021.
  • “Spinal Muscular Atrophy Awareness Discussion” Facebook Live organized by Integrated Health & Wellbeing (IHW) Council on 27th Aug 2021.
  • “Autism & Genomics” Organized by Lybrate GoodMD on 9th Mar 2021.
  • “Don’t Neglect Medical Genetics in Women’s Health” organized by the Obstetrics & Gynecology Society of Bangladesh on 10th Jan 2021.
  • "6th Edition of Year in Review Breast Cancer Conference" organized by Women’s Health Initiative by Tata Memorial Hospital, Mumbai held on 11th Jan 2021.
  • “Current status of Medical Genetics in India” Facebook Live organized by Cachar Chronicle on 18th Sep 20.
  • “Autism & Genomics” in Webinar on Insight into Autism & Fragile-X; organized by Indian Medical Association-Medical Student network in association with Fragile-X society, Indian on 22nd July 20.
  • “Our Experience of Chromosomal Microarray” in Celebrating 15 Years of Trusted Genomic Analysis with CGH on 26th Feb 20.
  • “Advanced Genetic Study with Interesting Case Scenarios” in Cloudnine-OAR Hospital on 11th Feb 20.
  • “Genetics in Clinical Practice” in Manipal Hospital, Goa on 8Th Jan 20.
  • “Genetic etiology of Developmental delay & disability” in CME on Developmental Pediatrics, SDUMC on 25th October 2019.
  • “Genetic disease Diagnosis & Gene therapy" in 41st CME in Internal Medicine organized by the Association of Physicians of India & Medical Education and Research Trust, Bangalore on 22th Sep 2019.
  • Panel discussion ‘CME on Anemia in Pregnancy; titled ‘The Pale Gravida’ - A Challenge !?!? on 22-Sep-2019, Bengaluru organized by The Society for Maternal-Fetal Medicine, (India).
  • A retrospective study of the profile and outcome of children with Dravet syndrome in a tertiary care hospital of Southern India, Journal of Pediatric Epilepsy (Accepted).
  • A novel mutation in GATA3 gene in a case of Hypoparathyroidism, Deafness and Renal dysplasia syndrome, Indian Journal of Nephrology (Accepted).
  • Sameeta M. Prabhu, Bidisha Banerjee, Ullas Acharya, Poonam P Hegde, Mitesh Shetty. MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes)—Usual and Unusual MRI Finding. Indian J Radiol Imaging https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0042-1755241.pdf.
  • Jyothsna Madan, Mitesh Shetty*, B S Ramamurthy, Surekha Managoli. “A Multidisciplinary approach for Prenatal diagnosis of FRASER SYNDROME - report of a novel variant in FRAS1.” Taiwanese Journal of Obstetrics and Gynecology, Volume 61(2022)129-132. https://doi.org/10.1016/j.tjog.2021.11.020.
  • Shetty M. “Genomics in infectious diseases” Pediatr Inf Dis 2021; 3 (2):57-64. https://www.pidjournal.com/doi/PID/pdf/10.5005/jp-journals-10081-1296.
  • Dr. Mitesh Shetty on More Bangaloreans take a genetic test to screen for future risk | Deccan Herald. Click Here

    Field of Expertise

  • Two decades of extensive experience in the field of Medical Genetics Prenatal diagnosis & Genetic counseling
  • Genetic diagnosis of Down syndrome, Autism, β-Thalassemia, Haemophilia, Duchenne muscular dystrophy (DMD) & Spinal muscular atrophy (SMA) etc.
  • Genetic counseling in consanguinity, recurrent abortions, Infertility, Pre- implantation Genetic Screening Test (PGT), Non-Invasive Prenatal Screening (NIPT/NIPS)
  • Expertise in Karyotyping, FISH study, Double/Quadruple study, Chromosomal Microarray & Next Generation Sequencing (NGS)
  • Risk assessment in hereditary cancer disorders like Breast & Ovarian cancer

    • Fellowship & Membership

  • Short-term Fellowship-Medical Genetics, York Hill Hospital, Glasgow, U.K.
  • European Board of Medical Genetics (EBMG).
  • Indian Society of Human Genetics (ISHG).
  • Indian Academy of Paediatrics-Genetics Specialty Chapter.
  • Bangalore Society of Obstetrics & Gynaecology.
  • Indian Society of Inborn Errors of Metabolism.
  • Indian Society of Prenatal Diagnosis & Therapy.
  • Molecular Pathology Association of India.

    • Languages Spoken

  • English
  • Hindi
  • Kannada
  • Tulu

    • Awards & Achievements

  • Faculty for a Certificate course in Genetic Counselling (MAHE).
  • Recognized Guide for Ph.D. in Manipal Academy of Higher Education (MAHE).
  • Guided Ph.D., M.Phil & MSc students & trained students for Genetic counseling.
  • Received IBM Sponsorship of CAS Project expenses towards clinical research.
  • Conducted a public awareness program on World Thalassemia Day (May 18) & World Down syndrome day (Mar 19).
  • Organized CME on “Integrating Genomics into Clinical Practice” (Jul 18) & “Autism awareness day” (Apr 19).
  • Published papers in National & International journals & CHAPTER IN BOOK-“Genetics in Congenital Heart Disease” In “A Comprehensive Approach to Congenital Heart Disease (A Lifelong Odyssey)” Jaypee brothers, ISBN 978-93-5090-267-7.

    • Talks & Publications

  • “Aneuploidy screening of sperm-is it useful? 26th Annual Conference organized by the Indian Society of Assisted Reproduction(ISAR)in Mumbai on 28th August.
  • “Genetic Counseling in Autism” organized by Manipal Advanced Centre for Child care on 17th April 2022.
  • “Genetic Testing to Shorten the Diagnostic Odyssey” organized by Manipal Advanced Centre for Child care on 13th April 2022.
  • “Down Syndrome Awareness Day 2022” organized by Rortact Club, Bangalore on 20th Mar 2022.
  • “IEM & Challenges in Prenatal Diagnosis” organized by NITTE University on 25th Feb 2022.
  • “Experience of chromosomal microarray applied in prenatal and postnatal settings “organized by Agilent India on 28th Jan 2022.
  • “Behind the scenes! Peek into the working of an NBS Lab” in the NATIONAL NEWBORN SCREENING SYMPOSIUM organized by the National Neonatal Forum India (NNFI) on 26th Sep 2021.
  • “Spinal Muscular Atrophy Awareness Discussion” Facebook Live organized by Integrated Health & Wellbeing (IHW) Council on 27th Aug 2021.
  • “Autism & Genomics” Organized by Lybrate GoodMD on 9th Mar 2021.
  • “Don’t Neglect Medical Genetics in Women’s Health” organized by the Obstetrics & Gynecology Society of Bangladesh on 10th Jan 2021.
  • "6th Edition of Year in Review Breast Cancer Conference" organized by Women’s Health Initiative by Tata Memorial Hospital, Mumbai held on 11th Jan 2021.
  • “Current status of Medical Genetics in India” Facebook Live organized by Cachar Chronicle on 18th Sep 20.
  • “Autism & Genomics” in Webinar on Insight into Autism & Fragile-X; organized by Indian Medical Association-Medical Student network in association with Fragile-X society, Indian on 22nd July 20.
  • “Our Experience of Chromosomal Microarray” in Celebrating 15 Years of Trusted Genomic Analysis with CGH on 26th Feb 20.
  • “Advanced Genetic Study with Interesting Case Scenarios” in Cloudnine-OAR Hospital on 11th Feb 20.
  • “Genetics in Clinical Practice” in Manipal Hospital, Goa on 8Th Jan 20.
  • “Genetic etiology of Developmental delay & disability” in CME on Developmental Pediatrics, SDUMC on 25th October 2019.
  • “Genetic disease Diagnosis & Gene therapy" in 41st CME in Internal Medicine organized by the Association of Physicians of India & Medical Education and Research Trust, Bangalore on 22th Sep 2019.
  • Panel discussion ‘CME on Anemia in Pregnancy; titled ‘The Pale Gravida’ - A Challenge !?!? on 22-Sep-2019, Bengaluru organized by The Society for Maternal-Fetal Medicine, (India).
  • A retrospective study of the profile and outcome of children with Dravet syndrome in a tertiary care hospital of Southern India, Journal of Pediatric Epilepsy (Accepted).
  • A novel mutation in GATA3 gene in a case of Hypoparathyroidism, Deafness and Renal dysplasia syndrome, Indian Journal of Nephrology (Accepted).
  • Sameeta M. Prabhu, Bidisha Banerjee, Ullas Acharya, Poonam P Hegde, Mitesh Shetty. MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes)—Usual and Unusual MRI Finding. Indian J Radiol Imaging https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0042-1755241.pdf.
  • Jyothsna Madan, Mitesh Shetty*, B S Ramamurthy, Surekha Managoli. “A Multidisciplinary approach for Prenatal diagnosis of FRASER SYNDROME - report of a novel variant in FRAS1.” Taiwanese Journal of Obstetrics and Gynecology, Volume 61(2022)129-132. https://doi.org/10.1016/j.tjog.2021.11.020.
  • Shetty M. “Genomics in infectious diseases” Pediatr Inf Dis 2021; 3 (2):57-64. https://www.pidjournal.com/doi/PID/pdf/10.5005/jp-journals-10081-1296.
  • Dr. Mitesh Shetty on More Bangaloreans take a genetic test to screen for future risk | Deccan Herald. Click Here

    Awards & Achievements

  • Faculty for a Certificate course in Genetic Counselling (MAHE).
  • Recognized Guide for Ph.D. in Manipal Academy of Higher Education (MAHE).
  • Guided Ph.D., M.Phil & MSc students & trained students for Genetic counseling.
  • Received IBM Sponsorship of CAS Project expenses towards clinical research.
  • Conducted a public awareness program on World Thalassemia Day (May 18) & World Down syndrome day (Mar 19).
  • Organized CME on “Integrating Genomics into Clinical Practice” (Jul 18) & “Autism awareness day” (Apr 19).
  • Published papers in National & International journals & CHAPTER IN BOOK-“Genetics in Congenital Heart Disease” In “A Comprehensive Approach to Congenital Heart Disease (A Lifelong Odyssey)” Jaypee brothers, ISBN 978-93-5090-267-7.

    • Fellowship & Membership

  • Short-term Fellowship-Medical Genetics, York Hill Hospital, Glasgow, U.K.
  • European Board of Medical Genetics (EBMG).
  • Indian Society of Human Genetics (ISHG).
  • Indian Academy of Paediatrics-Genetics Specialty Chapter.
  • Bangalore Society of Obstetrics & Gynaecology.
  • Indian Society of Inborn Errors of Metabolism.
  • Indian Society of Prenatal Diagnosis & Therapy.
  • Molecular Pathology Association of India.

    • Field of Expertise

  • Two decades of extensive experience in the field of Medical Genetics Prenatal diagnosis & Genetic counseling
  • Genetic diagnosis of Down syndrome, Autism, β-Thalassemia, Haemophilia, Duchenne muscular dystrophy (DMD) & Spinal muscular atrophy (SMA) etc.
  • Genetic counseling in consanguinity, recurrent abortions, Infertility, Pre- implantation Genetic Screening Test (PGT), Non-Invasive Prenatal Screening (NIPT/NIPS)
  • Expertise in Karyotyping, FISH study, Double/Quadruple study, Chromosomal Microarray & Next Generation Sequencing (NGS)
  • Risk assessment in hereditary cancer disorders like Breast & Ovarian cancer

    • Languages Spoken

  • English
  • Hindi
  • Kannada
  • Tulu

    • Talks & Publications

  • “Aneuploidy screening of sperm-is it useful? 26th Annual Conference organized by the Indian Society of Assisted Reproduction(ISAR)in Mumbai on 28th August.
  • “Genetic Counseling in Autism” organized by Manipal Advanced Centre for Child care on 17th April 2022.
  • “Genetic Testing to Shorten the Diagnostic Odyssey” organized by Manipal Advanced Centre for Child care on 13th April 2022.
  • “Down Syndrome Awareness Day 2022” organized by Rortact Club, Bangalore on 20th Mar 2022.
  • “IEM & Challenges in Prenatal Diagnosis” organized by NITTE University on 25th Feb 2022.
  • “Experience of chromosomal microarray applied in prenatal and postnatal settings “organized by Agilent India on 28th Jan 2022.
  • “Behind the scenes! Peek into the working of an NBS Lab” in the NATIONAL NEWBORN SCREENING SYMPOSIUM organized by the National Neonatal Forum India (NNFI) on 26th Sep 2021.
  • “Spinal Muscular Atrophy Awareness Discussion” Facebook Live organized by Integrated Health & Wellbeing (IHW) Council on 27th Aug 2021.
  • “Autism & Genomics” Organized by Lybrate GoodMD on 9th Mar 2021.
  • “Don’t Neglect Medical Genetics in Women’s Health” organized by the Obstetrics & Gynecology Society of Bangladesh on 10th Jan 2021.
  • "6th Edition of Year in Review Breast Cancer Conference" organized by Women’s Health Initiative by Tata Memorial Hospital, Mumbai held on 11th Jan 2021.
  • “Current status of Medical Genetics in India” Facebook Live organized by Cachar Chronicle on 18th Sep 20.
  • “Autism & Genomics” in Webinar on Insight into Autism & Fragile-X; organized by Indian Medical Association-Medical Student network in association with Fragile-X society, Indian on 22nd July 20.
  • “Our Experience of Chromosomal Microarray” in Celebrating 15 Years of Trusted Genomic Analysis with CGH on 26th Feb 20.
  • “Advanced Genetic Study with Interesting Case Scenarios” in Cloudnine-OAR Hospital on 11th Feb 20.
  • “Genetics in Clinical Practice” in Manipal Hospital, Goa on 8Th Jan 20.
  • “Genetic etiology of Developmental delay & disability” in CME on Developmental Pediatrics, SDUMC on 25th October 2019.
  • “Genetic disease Diagnosis & Gene therapy" in 41st CME in Internal Medicine organized by the Association of Physicians of India & Medical Education and Research Trust, Bangalore on 22th Sep 2019.
  • Panel discussion ‘CME on Anemia in Pregnancy; titled ‘The Pale Gravida’ - A Challenge !?!? on 22-Sep-2019, Bengaluru organized by The Society for Maternal-Fetal Medicine, (India).
  • A retrospective study of the profile and outcome of children with Dravet syndrome in a tertiary care hospital of Southern India, Journal of Pediatric Epilepsy (Accepted).
  • A novel mutation in GATA3 gene in a case of Hypoparathyroidism, Deafness and Renal dysplasia syndrome, Indian Journal of Nephrology (Accepted).
  • Sameeta M. Prabhu, Bidisha Banerjee, Ullas Acharya, Poonam P Hegde, Mitesh Shetty. MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes)—Usual and Unusual MRI Finding. Indian J Radiol Imaging https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0042-1755241.pdf.
  • Jyothsna Madan, Mitesh Shetty*, B S Ramamurthy, Surekha Managoli. “A Multidisciplinary approach for Prenatal diagnosis of FRASER SYNDROME - report of a novel variant in FRAS1.” Taiwanese Journal of Obstetrics and Gynecology, Volume 61(2022)129-132. https://doi.org/10.1016/j.tjog.2021.11.020.
  • Shetty M. “Genomics in infectious diseases” Pediatr Inf Dis 2021; 3 (2):57-64. https://www.pidjournal.com/doi/PID/pdf/10.5005/jp-journals-10081-1296.
  • Dr. Mitesh Shetty on More Bangaloreans take a genetic test to screen for future risk | Deccan Herald. Click Here

    Talks & Publications

  • “Aneuploidy screening of sperm-is it useful? 26th Annual Conference organized by the Indian Society of Assisted Reproduction(ISAR)in Mumbai on 28th August.
  • “Genetic Counseling in Autism” organized by Manipal Advanced Centre for Child care on 17th April 2022.
  • “Genetic Testing to Shorten the Diagnostic Odyssey” organized by Manipal Advanced Centre for Child care on 13th April 2022.
  • “Down Syndrome Awareness Day 2022” organized by Rortact Club, Bangalore on 20th Mar 2022.
  • “IEM & Challenges in Prenatal Diagnosis” organized by NITTE University on 25th Feb 2022.
  • “Experience of chromosomal microarray applied in prenatal and postnatal settings “organized by Agilent India on 28th Jan 2022.
  • “Behind the scenes! Peek into the working of an NBS Lab” in the NATIONAL NEWBORN SCREENING SYMPOSIUM organized by the National Neonatal Forum India (NNFI) on 26th Sep 2021.
  • “Spinal Muscular Atrophy Awareness Discussion” Facebook Live organized by Integrated Health & Wellbeing (IHW) Council on 27th Aug 2021.
  • “Autism & Genomics” Organized by Lybrate GoodMD on 9th Mar 2021.
  • “Don’t Neglect Medical Genetics in Women’s Health” organized by the Obstetrics & Gynecology Society of Bangladesh on 10th Jan 2021.
  • "6th Edition of Year in Review Breast Cancer Conference" organized by Women’s Health Initiative by Tata Memorial Hospital, Mumbai held on 11th Jan 2021.
  • “Current status of Medical Genetics in India” Facebook Live organized by Cachar Chronicle on 18th Sep 20.
  • “Autism & Genomics” in Webinar on Insight into Autism & Fragile-X; organized by Indian Medical Association-Medical Student network in association with Fragile-X society, Indian on 22nd July 20.
  • “Our Experience of Chromosomal Microarray” in Celebrating 15 Years of Trusted Genomic Analysis with CGH on 26th Feb 20.
  • “Advanced Genetic Study with Interesting Case Scenarios” in Cloudnine-OAR Hospital on 11th Feb 20.
  • “Genetics in Clinical Practice” in Manipal Hospital, Goa on 8Th Jan 20.
  • “Genetic etiology of Developmental delay & disability” in CME on Developmental Pediatrics, SDUMC on 25th October 2019.
  • “Genetic disease Diagnosis & Gene therapy" in 41st CME in Internal Medicine organized by the Association of Physicians of India & Medical Education and Research Trust, Bangalore on 22th Sep 2019.
  • Panel discussion ‘CME on Anemia in Pregnancy; titled ‘The Pale Gravida’ - A Challenge !?!? on 22-Sep-2019, Bengaluru organized by The Society for Maternal-Fetal Medicine, (India).
  • A retrospective study of the profile and outcome of children with Dravet syndrome in a tertiary care hospital of Southern India, Journal of Pediatric Epilepsy (Accepted).
  • A novel mutation in GATA3 gene in a case of Hypoparathyroidism, Deafness and Renal dysplasia syndrome, Indian Journal of Nephrology (Accepted).
  • Sameeta M. Prabhu, Bidisha Banerjee, Ullas Acharya, Poonam P Hegde, Mitesh Shetty. MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes)—Usual and Unusual MRI Finding. Indian J Radiol Imaging https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0042-1755241.pdf.
  • Jyothsna Madan, Mitesh Shetty*, B S Ramamurthy, Surekha Managoli. “A Multidisciplinary approach for Prenatal diagnosis of FRASER SYNDROME - report of a novel variant in FRAS1.” Taiwanese Journal of Obstetrics and Gynecology, Volume 61(2022)129-132. https://doi.org/10.1016/j.tjog.2021.11.020.
  • Shetty M. “Genomics in infectious diseases” Pediatr Inf Dis 2021; 3 (2):57-64. https://www.pidjournal.com/doi/PID/pdf/10.5005/jp-journals-10081-1296.
  • Dr. Mitesh Shetty on More Bangaloreans take a genetic test to screen for future risk | Deccan Herald. Click Here

    • Fellowship & Membership

  • Short-term Fellowship-Medical Genetics, York Hill Hospital, Glasgow, U.K.
  • European Board of Medical Genetics (EBMG).
  • Indian Society of Human Genetics (ISHG).
  • Indian Academy of Paediatrics-Genetics Specialty Chapter.
  • Bangalore Society of Obstetrics & Gynaecology.
  • Indian Society of Inborn Errors of Metabolism.
  • Indian Society of Prenatal Diagnosis & Therapy.
  • Molecular Pathology Association of India.

    • Field of Expertise

  • Two decades of extensive experience in the field of Medical Genetics Prenatal diagnosis & Genetic counseling
  • Genetic diagnosis of Down syndrome, Autism, β-Thalassemia, Haemophilia, Duchenne muscular dystrophy (DMD) & Spinal muscular atrophy (SMA) etc.
  • Genetic counseling in consanguinity, recurrent abortions, Infertility, Pre- implantation Genetic Screening Test (PGT), Non-Invasive Prenatal Screening (NIPT/NIPS)
  • Expertise in Karyotyping, FISH study, Double/Quadruple study, Chromosomal Microarray & Next Generation Sequencing (NGS)
  • Risk assessment in hereditary cancer disorders like Breast & Ovarian cancer

    • Languages Spoken

  • English
  • Hindi
  • Kannada
  • Tulu

    • Awards & Achievements

  • Faculty for a Certificate course in Genetic Counselling (MAHE).
  • Recognized Guide for Ph.D. in Manipal Academy of Higher Education (MAHE).
  • Guided Ph.D., M.Phil & MSc students & trained students for Genetic counseling.
  • Received IBM Sponsorship of CAS Project expenses towards clinical research.
  • Conducted a public awareness program on World Thalassemia Day (May 18) & World Down syndrome day (Mar 19).
  • Organized CME on “Integrating Genomics into Clinical Practice” (Jul 18) & “Autism awareness day” (Apr 19).
  • Published papers in National & International journals & CHAPTER IN BOOK-“Genetics in Congenital Heart Disease” In “A Comprehensive Approach to Congenital Heart Disease (A Lifelong Odyssey)” Jaypee brothers, ISBN 978-93-5090-267-7.

Doctor Videos

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Mar 23,2022

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Mar 20,2020

Autism Spectrum Disorder: Causes and Symptoms

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Hemophilia: Causes, Symptoms, and Prevention

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