Anju
@AnjuShukla21
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Clinical geneticist at KMC Manipal
Joined January 2021
RT @Sanjiba06972691: Excited to share our latest collaborative paper with @AnjuShukla21, @Lab_Pandey, @aartvi42. Thank you @ICMRDELHI, @MSL….
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RT @India_Alliance: In support of #RareDiseaseDay2025, we’re highlighting our researchers working to improve rare diseases diagnosis, treat….
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RT @ramdam1982: The Dept. of Medical Genetics, KMC Manipal organized a powerful street play yesterday to 📢 spread awareness about rare dise….
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Looking for enthusiastic young project manager, please see the advertisement below @India_Alliance @MAHE_Manipal @kmc_manipal
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RT @eshgsociety: A warm welcome from the new president of the #societyforhumangenetics @GeneticBill! As the website is already live, check….
2025.eshg.org
ESHG 2022 COVID-19 Information Discover the ESHG 2025 - Hybrid Conference programme. We are proud to announce the confirmed 2025 speakers. Stay updated on matters related to the ESHG society. Thank...
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RT @RMaroofian: Our new study identifies biallelic EPB41L3 variants linked to a regressive neurodevelopmental disorder characterized by ear….
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RT @AmirInScience: Exciting news! Join us at the "Mitochondrial Genomics: from Mutation to Clinical Phenotypes” on July 27, 2024 at @MSLS_M….
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RT @GenomeKumar: WELCOME TO THE PINK CITY OF INDIA- PARTICIPATE IN THE ICBD2024 28-30 NOVEMBER 2024!
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Research fellow position available to work on interesting aspects of rare genetic diseases @GeneticsManipal @kmc_manipal @MAHE_Manipal, please RT
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Exciting opportunity to work with a enthusiastic team on rare diseases @kmc_manipal @MAHE_Manipal @GeneticsManipal. Request to spread the word, last date of application is July 31.
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RT @mft_iMRare: We are delighted to announce the European Society of Human Genetics Syndromology and Dysmophology Course in Manchester - 22….
mrcc.org.uk
We are delighted to announce the Manchester European Society of Human Genetics Syndromology and Dysmorphology Course 2024*. This course is primarily aimed at Clinical Geneticists in training but will...
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RT @GeneticsManipal: "Thank you to everyone who joined us for an incredible #OpenDay2024 🧬.Your curiosity and enthusiasm made it a memorabl….
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RT @KMC_Socialmedia: 🌟 Highlights."Cracking the genetic code of the human genome".🧬 Interactive sessions on rare genetic disorders, DNA ext….
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RT @SofiaDouzgou: News about the @eshgsociety Dysmorphology workshops! A dedicated pre-submission portal and, the ‘Dian Donnai and Jill Cl….
2024.eshg.org
Dysmorphology Case submission is now closed. The submission deadline was Tuesday, April 16, 2024 at 23:59 hrs CEST. The first ESHG Dysmorphology workshop run in Genoa, in 1997, by Dian Donnai and...
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RT @India_Alliance: We celebrate contributions of women in biomedical research in India & are proud to support the brilliant minds as they….
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We are committed to the cause of families with rare genetic disorders @GeneticsManipal @kmc_manipal @BhatVivekananda @pe_radhakrishna @PUpadhyai @ShaliniSNayak1 @MAHE_Manipal
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RT @TIGS_India: Are you participating at the annual #Racefor7 event? . An awareness run about #rarediseases and to empower patients and the….
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RT @MAHE_Manipal: 🎓 Manipal Academy of Higher Education (MAHE), an Institution of Eminence Deemed to be University, Manipal, welcomes appli….
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RT @MajethiaPurvi: Thrilled to share that our paper, "Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families:….
onlinelibrary.wiley.com
The current study highlights the phenotypic and genotypic insights from 142 Indian families with epilepsy with or without comorbidities. We further study its implications on genetic counseling and...
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