Using a common biomarker across 11 different tumour types to detect a common hereditary cancer predisposition syndrome, data from India's largest study shows.
\n", "date_published": "2026-10-07T07:58:00.000Z", "tags": [ "research", "publication" ] }, { "id": "https://geneticcentre.org/news/first-comprehensive-characterisation-of-niemann-pick-c-disease-in-india/", "url": "https://geneticcentre.org/news/first-comprehensive-characterisation-of-niemann-pick-c-disease-in-india/", "title": "First comprehensive characterisation of Niemann-Pick C disease in India", "summary": "FRIGE scientists leads India's 16 year study on comprehensive clinical and molecular characterisation of an ultra-rare disorder in India.", "content_html": "FRIGE scientists leads India's 16 year study on comprehensive clinical and molecular characterisation of an ultra-rare disorder in India.
\n", "date_published": "2026-09-04T09:32:51.336Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/frige-internship-and-training-program-(winter-edition-2026)/", "url": "https://geneticcentre.org/news/frige-internship-and-training-program-(winter-edition-2026)/", "title": "FRIGE - Internship and Training Program (Winter Edition 2026)", "summary": "Genetics is currently going through a rapid expansion in its suite of techniques and technologies. Understanding these technologies and utilising them in clinical research and diagnostic settings is key for their robust implementation in clinics.", "content_html": "Genetics is currently going through a rapid expansion in its suite of techniques and technologies. Understanding these technologies and utilising them in clinical research and diagnostic settings is key for their robust implementation in clinics.
\n", "date_published": "2026-09-02T10:11:53.498Z", "tags": [ "training" ] }, { "id": "https://geneticcentre.org/news/advertisement-for-two-junior-research-fellows-for-cutting-edge-research/", "url": "https://geneticcentre.org/news/advertisement-for-two-junior-research-fellows-for-cutting-edge-research/", "title": "Advertisement for two Junior Research Fellows for cutting edge research", "summary": "We are a world class research-intensive institute. We deliver clinical diagnostics, genetic counselling, teaching and R&D of the highest quality. Attracting and retaining high-calibre people is fundamental to our continued success.", "content_html": "We are a world class research-intensive institute. We deliver clinical diagnostics, genetic counselling, teaching and R&D of the highest quality. Attracting and retaining high-calibre people is fundamental to our continued success.
\n", "date_published": "2026-08-09T12:39:44.257Z", "tags": [ "jobs" ] }, { "id": "https://geneticcentre.org/news/frige-internship-and-training-program-(summer-edition-2026)/", "url": "https://geneticcentre.org/news/frige-internship-and-training-program-(summer-edition-2026)/", "title": "FRIGE - Internship and Training Program (Summer Edition 2026)", "summary": "Genetics is currently going through a rapid expansion in its suite of techniques and technologies. Understanding these technologies and utilising them in clinical research and diagnostic settings is key for their robust implementation in clinics.", "content_html": "Genetics is currently going through a rapid expansion in its suite of techniques and technologies. Understanding these technologies and utilising them in clinical research and diagnostic settings is key for their robust implementation in clinics.
\n", "date_published": "2026-02-25T12:30:38.523Z", "tags": [ "training" ] }, { "id": "https://geneticcentre.org/news/frige-scientists-develop-india's-first-national-biobank-for-lysosomal-storage-disorders/", "url": "https://geneticcentre.org/news/frige-scientists-develop-india's-first-national-biobank-for-lysosomal-storage-disorders/", "title": "FRIGE scientists develop India's first national biobank for Lysosomal Storage Disorders", "summary": "Scientists develop and deploy India's first national biobank for rare disease- Lysosomal Storage Disorders- comprising of over 500 patients.", "content_html": "Scientists develop and deploy India's first national biobank for rare disease- Lysosomal Storage Disorders- comprising of over 500 patients.
\n", "date_published": "2026-02-06T09:13:49.021Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/breakthrough-in-understanding-the-genetic-cause-of-severe-male-infertility-in-india/", "url": "https://geneticcentre.org/news/breakthrough-in-understanding-the-genetic-cause-of-severe-male-infertility-in-india/", "title": "Breakthrough in understanding the genetic cause of severe male infertility in India", "summary": "Sequencing based technology is developing a new paradigm in understanding the cause and providing tailored reproductive options to men with infertility, data from a large cohort shows.", "content_html": "Sequencing based technology is developing a new paradigm in understanding the cause and providing tailored reproductive options to men with infertility, data from a large cohort shows.
\n", "date_published": "2025-12-26T11:48:09.996Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/advertisement-for-two-junior-research-fellows/", "url": "https://geneticcentre.org/news/advertisement-for-two-junior-research-fellows/", "title": "Advertisement for two Junior Research Fellows", "summary": "We are a world class research-intensive institute. We deliver clinical diagnostics, genetic counselling, teaching and R&D of the highest quality. Attracting and retaining high-calibre people is fundamental to our continued success.", "content_html": "We are a world class research-intensive institute. We deliver clinical diagnostics, genetic counselling, teaching and R&D of the highest quality. Attracting and retaining high-calibre people is fundamental to our continued success.
\n", "date_published": "2025-11-30T05:40:20.471Z", "tags": [ "jobs" ] }, { "id": "https://geneticcentre.org/news/advertisement-for-research-associate/", "url": "https://geneticcentre.org/news/advertisement-for-research-associate/", "title": "Advertisement for Research Associate", "summary": "We are a world class diagnostics and research-intensive institute. We deliver clinical diagnostics, genetic counselling, teaching and R&D of the highest quality. Attracting and retaining high-caliber people is fundamental to our continued success.", "content_html": "Genetics is currently going through a rapid expansion in its suite of techniques and technologies. Understanding these technologies and utilising them in clinical research and diagnostic settings is key for their robust implementation in clinics.
\n", "date_published": "2025-09-11T09:01:12.808Z", "tags": [ "training" ] }, { "id": "https://geneticcentre.org/news/frige-scientists-analyse-utility-of-prenatal-diagnosis-for-preventing-rare-genetic-disorders-in-india/", "url": "https://geneticcentre.org/news/frige-scientists-analyse-utility-of-prenatal-diagnosis-for-preventing-rare-genetic-disorders-in-india/", "title": "FRIGE scientists analyse utility of prenatal diagnosis for preventing rare genetic disorders in India", "summary": "Systematic analysis of data of over 1700 prenatal samples from tertiary centre during 14 year period shows ~25% babies affected with a genetic disease.", "content_html": "Systematic analysis of data of over 1700 prenatal samples from tertiary centre during 14 year period shows ~25% babies affected with a genetic disease.
\n", "date_published": "2025-09-02T14:59:13.137Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/frige-scientists-decipher-role-of-structural-variants-in-autism/", "url": "https://geneticcentre.org/news/frige-scientists-decipher-role-of-structural-variants-in-autism/", "title": "FRIGE scientists decipher role of structural variants in autism", "summary": "India's first systematic and cutting-edge genetic study in 23 children with autism spectrum disorder explored the role of long-read whole genome sequencing and structural variants in the cause of autism.", "content_html": "India's first systematic and cutting-edge genetic study in 23 children with autism spectrum disorder explored the role of long-read whole genome sequencing and structural variants in the cause of autism.
\n", "date_published": "2025-08-20T15:02:18.737Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/frige-internship-training-and-dissertation-program-(summer-edition-2025)/", "url": "https://geneticcentre.org/news/frige-internship-training-and-dissertation-program-(summer-edition-2025)/", "title": "FRIGE - Internship, Training and Dissertation Program (Summer Edition 2025)", "summary": "Genetics is currently going through a rapid expansion in its suite of techniques and technologies. Understanding these technologies and utilising them in clinical research and diagnostic settings is key for their robust implementation in clinics.", "content_html": "Genetics is currently going through a rapid expansion in its suite of techniques and technologies. Understanding these technologies and utilising them in clinical research and diagnostic settings is key for their robust implementation in clinics.
\n", "date_published": "2025-03-17T06:22:24.342Z", "tags": [ "training" ] }, { "id": "https://geneticcentre.org/news/advertisement-for-a-junior-research-fellow-molecular-genetics/", "url": "https://geneticcentre.org/news/advertisement-for-a-junior-research-fellow-molecular-genetics/", "title": "Advertisement for a Junior Research Fellow- Molecular Genetics", "summary": "We are a world class diagnostics and research-intensive institute. We deliver clinical diagnostics, genetic counselling, teaching and R&D of the highest quality. Attracting and retaining high-calibre people is fundamental to our continued success.", "content_html": "We are a world class diagnostics and research-intensive institute. We deliver clinical diagnostics, genetic counselling, teaching and R&D of the highest quality. Attracting and retaining high-calibre people is fundamental to our continued success.
\n", "date_published": "2025-01-13T09:05:31.928Z", "tags": [ "jobs" ] }, { "id": "https://geneticcentre.org/news/frige-scientists-discover-india's-first-founder-variant-in-mlh1-gene-associated-with-lynch-syndrome/", "url": "https://geneticcentre.org/news/frige-scientists-discover-india's-first-founder-variant-in-mlh1-gene-associated-with-lynch-syndrome/", "title": "FRIGE scientists discover India's first founder variant in MLH1 gene associated with Lynch syndrome", "summary": "Founder variant that is observed in approximately 6.4% of all Lynch syndrome patients, the most common hereditary cancer disease, has been discovered.", "content_html": "Founder variant that is observed in approximately 6.4% of all Lynch syndrome patients, the most common hereditary cancer disease, has been discovered.
\n", "date_published": "2024-12-19T02:26:07.794Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/frige-scientists-analyse-burden-of-complex-chromosomal-rearrangements-in-india/", "url": "https://geneticcentre.org/news/frige-scientists-analyse-burden-of-complex-chromosomal-rearrangements-in-india/", "title": "FRIGE scientists analyse burden of complex chromosomal rearrangements in India", "summary": "Systematic analysis of data of over 4200 couples with clinical history of repeated foetal loss from tertiary centre during 30 year period shows role of complex chromosomal rearrangements.", "content_html": "Systematic analysis of data of over 4200 couples with clinical history of repeated foetal loss from tertiary centre during 30 year period shows role of complex chromosomal rearrangements.
\n", "date_published": "2024-11-19T12:03:44.988Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/frige-part-of-the-international-human-ring-chromosome-consoritum/", "url": "https://geneticcentre.org/news/frige-part-of-the-international-human-ring-chromosome-consoritum/", "title": "FRIGE part of the International Human Ring Chromosome consortium", "summary": "A large international collaboration consisting of teams from USA, UK, Europe and India are working together to understand the incidence, aetiology, detection mechanisms and guideline preparation.", "content_html": "A large international collaboration consisting of teams from USA, UK, Europe and India are working together to understand the incidence, aetiology, detection mechanisms and guideline preparation.
\n", "date_published": "2024-11-16T06:08:20.315Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/frige-scientists-analyse-burden-of-rare-genetic-disorders-in-india/", "url": "https://geneticcentre.org/news/frige-scientists-analyse-burden-of-rare-genetic-disorders-in-india/", "title": "FRIGE scientists analyse burden of rare genetic disorders in India", "summary": "Systematic analysis of data of over 3000 patients from tertiary centre during 22 year period shows 3000 patients with rare genetic diseases across 14 major disease groups.", "content_html": "Systematic analysis of data of over 3000 patients from tertiary centre during 22 year period shows 3000 patients with rare genetic diseases across 14 major disease groups.
\n", "date_published": "2024-10-23T14:36:32.076Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/frige-sanofi-disha-program:-free-of-cost-diagnosis-for-common-lysosomal-storage-disorders/", "url": "https://geneticcentre.org/news/frige-sanofi-disha-program:-free-of-cost-diagnosis-for-common-lysosomal-storage-disorders/", "title": "FRIGE-Sanofi DISHA Program: Free of cost diagnosis for common lysosomal storage disorders", "summary": "FRIGE and Sanofi have partnered to develop DISHA program- a comprehensive program for diagnosis of common lysosomal storage disorders in India.", "content_html": "FRIGE and Sanofi have partnered to develop DISHA program- a comprehensive program for diagnosis of common lysosomal storage disorders in India.
\n", "date_published": "2024-10-20T20:55:05.173Z", "tags": [ "diagnostic test" ] }, { "id": "https://geneticcentre.org/news/30th-anniversary-of-genetics-pioneer-institution/", "url": "https://geneticcentre.org/news/30th-anniversary-of-genetics-pioneer-institution/", "title": "30th Anniversary of Genetics Pioneer Institution", "summary": "An institution that started from a small room with a dining table has metamorphized into a state-of-art diagnostics and translation research powerhouse in the arena of genetics and genomics in India.", "content_html": "An institution that started from a small room with a dining table has metamorphized into a state-of-art diagnostics and translation research powerhouse in the arena of genetics and genomics in India.
\n", "date_published": "2024-10-18T14:12:17.641Z", "tags": [ "public engagement" ] }, { "id": "https://geneticcentre.org/news/advertisement-for-a-senior-cytogeneticist/", "url": "https://geneticcentre.org/news/advertisement-for-a-senior-cytogeneticist/", "title": "Advertisement for a Senior Cytogeneticist", "summary": "We are a world class diagnostics and research-intensive institute. We deliver clinical diagnostics, genetic counselling, teaching and R&D of the highest quality. Attracting and retaining high-calibre people is fundamental to our continued success.", "content_html": "We are a world class diagnostics and research-intensive institute. We deliver clinical diagnostics, genetic counselling, teaching and R&D of the highest quality. Attracting and retaining high-calibre people is fundamental to our continued success.
\n", "date_published": "2024-09-20T03:45:49.252Z", "tags": [ "jobs" ] }, { "id": "https://geneticcentre.org/news/frige-internship-training-and-dissertation-program-(winter-edition)/", "url": "https://geneticcentre.org/news/frige-internship-training-and-dissertation-program-(winter-edition)/", "title": "FRIGE - Internship, Training and Dissertation Program (Winter Edition)", "summary": "Genetics is currently going through a rapid expansion in its suite of techniques and technologies. Understanding these technologies and utilising them in clinical research and diagnostic settings is key for their robust implementation in clinics.", "content_html": "Genetics is currently going through a rapid expansion in its suite of techniques and technologies. Understanding these technologies and utilising them in clinical research and diagnostic settings is key for their robust implementation in clinics.
\n", "date_published": "2024-09-02T12:31:19.209Z", "tags": [ "public engagement" ] }, { "id": "https://geneticcentre.org/news/celebrating-autism-awareness-month-and-world-parkinson-day/", "url": "https://geneticcentre.org/news/celebrating-autism-awareness-month-and-world-parkinson-day/", "title": "Celebrating Autism awareness month and World Parkinson Day", "summary": "With neurological disorders on the rise, understanding their cause, diagnostic methods, management, treatment and prevention is ever more crucial than before.", "content_html": "With neurological disorders on the rise, understanding their cause, diagnostic methods, management, treatment and prevention is ever more crucial than before.
\n", "date_published": "2024-04-15T15:28:12.139Z", "tags": [ "public engagement" ] }, { "id": "https://geneticcentre.org/news/frige-scientists-initiate-study-on-hereditary-cancer/", "url": "https://geneticcentre.org/news/frige-scientists-initiate-study-on-hereditary-cancer/", "title": "FRIGE scientists initiate study on hereditary cancer", "summary": "India's first systematic epidemiological study on the genetic contribution behind common cancers begins.", "content_html": "India's first systematic epidemiological study on the genetic contribution behind common cancers begins.
\n", "date_published": "2024-03-18T14:45:54.963Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/improving-understanding-of-the-role-of-neurog1-gene-in-autism/", "url": "https://geneticcentre.org/news/improving-understanding-of-the-role-of-neurog1-gene-in-autism/", "title": "Improving understanding of the role of NEUROG1 gene in autism", "summary": "A large study in Indian children with autism identified NEUROG1 to play a role in causing autism spectrum disorder together with cranial dysinnervation syndrome.", "content_html": "A large study in Indian children with autism identified NEUROG1 to play a role in causing autism spectrum disorder together with cranial dysinnervation syndrome.
\n", "date_published": "2024-02-16T12:33:00.826Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/48th-annual-meeting-and-international-conference-of-the-indian-society-of-human-genetics/", "url": "https://geneticcentre.org/news/48th-annual-meeting-and-international-conference-of-the-indian-society-of-human-genetics/", "title": "48th Annual Meeting and International Conference of the Indian Society of Human Genetics", "summary": "India's biggest human genetics and genomics meet of 2024 is organised by the Foundation for Research in Genetics and Endocrinology along with Gujarat Biotechnology Research Centre.", "content_html": "India's biggest human genetics and genomics meet of 2024 is organised by the Foundation for Research in Genetics and Endocrinology along with Gujarat Biotechnology Research Centre.
\n", "date_published": "2023-08-14T10:34:08.686Z", "tags": [ "public engagement" ] }, { "id": "https://geneticcentre.org/news/frige-scientists-decipher-genetic-architecture-of-autism-in-india/", "url": "https://geneticcentre.org/news/frige-scientists-decipher-genetic-architecture-of-autism-in-india/", "title": "FRIGE scientists decipher genetic architecture of autism in India", "summary": "India's first systematic genetic study in 101 children with autism spectrum disorder has shown a significant contribution of de novo mutation towards aetiology of ASD.", "content_html": "India's first systematic genetic study in 101 children with autism spectrum disorder has shown a significant contribution of de novo mutation towards aetiology of ASD.
\n", "date_published": "2023-08-05T08:14:01.522Z", "tags": [ "research" ] }, { "id": "https://geneticcentre.org/news/frige-and-dr-jivraj-mehta-hospital-join-hands-to-create-state-of-the-art-genetics-opd-in-public-hospital/", "url": "https://geneticcentre.org/news/frige-and-dr-jivraj-mehta-hospital-join-hands-to-create-state-of-the-art-genetics-opd-in-public-hospital/", "title": "FRIGE and Dr Jivraj Mehta Hospital join hands to create state-of-the-art Genetics OPD in public hospital", "summary": "FRIGE and Dr. Jivraj Mehta Hospital begin a new chapter in personalised, precision and preventative healthcare by launching the first genetics OPD at the hospital.", "content_html": "FRIGE and Dr. Jivraj Mehta Hospital begin a new chapter in personalised, precision and preventative healthcare by launching the first genetics OPD at the hospital.
\n", "date_published": "2023-02-09T15:46:11.092Z", "tags": [ "news" ] }, { "id": "https://geneticcentre.org/news/nobel-prize-in-physiology-or-medicine-2022-ancient-human-dna-and-human-evolution/", "url": "https://geneticcentre.org/news/nobel-prize-in-physiology-or-medicine-2022-ancient-human-dna-and-human-evolution/", "title": "Nobel Prize in Physiology or Medicine 2022- Ancient Human DNA and Human Evolution", "summary": "Svante Paabo made pathbreaking discoveries on human evolution using ancient DNA of Neanderthals and Denisovans- and his work spawned the field of palaeogenomics.", "content_html": "Svante Paabo made pathbreaking discoveries on human evolution using ancient DNA of Neanderthals and Denisovans- and his work spawned the field of palaeogenomics.
\n", "date_published": "2022-10-06T17:16:15.920Z", "tags": [ "news" ] }, { "id": "https://geneticcentre.org/news/daily-resistant-starch-prevents-cancers-in-lynch-syndrome-patients/", "url": "https://geneticcentre.org/news/daily-resistant-starch-prevents-cancers-in-lynch-syndrome-patients/", "title": "Daily resistant starch prevents cancers in Lynch syndrome patients", "summary": "A randomised controlled trial in people with Lynch syndrome has shown a significant cancer prevention effect from resistant starch, found in a range of daily food items such as slightly green bananas and oats.", "content_html": "A randomised controlled trial in people with Lynch syndrome has shown a significant cancer prevention effect from resistant starch, found in a range of daily food items such as slightly green bananas and oats.
\n", "date_published": "2022-07-26T12:08:00.156Z", "tags": [ "research" ] } ] }