Dr. Emili Banerjee – Sashthashree Diagnostic Center

Dr. Emili Banerjee Bhattacharjee (Ph. D., Post Doc., CGC)

Senior Genetic Counsellor
BGCI Certified Genetic Counsellor (Level II)
HSSC Certified Genetic Counseling Trainer v3.0
Attached as a Genetic Counsellor in
➢ NOVA IVF-fertility centre, Kolkata
➢ Raindrops Hospital, Bally, Howrah
➢ Sampurna Women Care and IVF, Kolkata
➢ Ankur Fertility Clinic, New Alipore, Kolkata
➢ GENOME the fertility Centre, Kolkata
➢ Institute of Fetal Medicine, Kolkata
➢ Mon Amie- Women’s Clinic & IVF Center, Barasat
➢ Sumaang Health Care, Near Kolkata Airport, Dumdum

Mob: +919831258473
Email: banerjeeemily@yahoo.com; dremili.geneticist@gmail.com

EDUCATION AND QUALIFICATIONS

M. Sc in Zoology with specialization in “Cell and Molecular Biology”, University Silver Medalist, North Bengal University, 2002.
Ph. D. in Biotechnology, University of Calcutta, 2010.
Post Doc (4 years, as DBT-RA) Molecular Neuropathology underlying Perkinson’s Disease, CSIR-IICB, Kolkata, 2010 – 2013.
Certificate in Genetic Counselling, Indian Medical Association (2021) and University of Manchester & Welcome Connecting Science, UK (2022).
BGCI-Certified Genetic Counsellor Level II (Membership Number – 2023-257)

AWARDS AND HONOURS

• Acting as “Manuscript Reviewer” in the prestigious science journal “Scientific Reports” (Springer-Nature), continuously and has reviewed several manuscripts.
• Best Paper Award, National Genetic Counseling Symposium, March 7-8 2025, BRIC-CDFD, Hyderabad, India.
• APSN-ISN-IBRO school award for attending neuroscience school in Osaka, Japan 2012.
• S.S.Parmar Research Foundation Award for best poster presentation in International symposium on recent trends in neurosciences & XXIX annual conference of Indian Academy of Neurosciences. 2011, New Delhi, India.
• January 1st 2010- 2013: Recipient of Post-doctoral Fellowship (Research Associateship) from Department of Biotechnology, Govt. of India.
• May 2007- May 2009: Recipient of Senior Research Fellowship from Council of Scientific and Industrial Research (CSIR).
• April 2007: Awarded Senior Research Fellowship from Indian Council of Medical Research (ICMR) (declined).
• April 2006: Travel grant from the Department of Biotechnology, Govt. of India for attending the workshop on “Diagnosis of Genetic Disorders Using Cytogenetics & Molecular Genetics Methods” organized by Departments of Pediatrics, Anatomy &
Hematology, All India Institute of Medical Sciences, New Delhi, April 17th -26th, 2006.
• 2002: University Silver Medal for 2 nd rank in M.Sc Examination, North Bengal University.

CME, RTM, PANEL DISCUSSION, AND INVITED LECTURES DONE

• Faculty Chairperson in Panel discussion on “Genetics of Polycystic Kidney Disorder” on 8th June, 2025 at PIXELS TO PROGNOSIS, the Annual Conference of Society for Fetal Medicine, Bengal Chapter.
• CME lecture on “Genetic Testing in Clinical Settings – A Case Based Approach and Discussion” on 15th May, 2025 organized by Department of Endocrinology, Vivekananda Institute of Medical Science, Ramakrishna Mission Seva Prathisthan, Kolkata, West Bengal.
• Webinar lecture on “Genetics for Clinicians – The Basic” on 7th May, 2025 organized by Patna Chapter of Perinatology and Reproductive Biology, Patna, Bihar.
• RTM lecture on “Genetic Testing in Neurodevelopmental Disorders: Unravelling The Cause Behind” at organized by Department of Neurology, Sir Nilratan Sircar Medical College and Hospital, Kolkata, West Bengal.
• CME lecture on “Fetal medicine and genetics: The Hand and Glove” at “Feto Connect – Let’s Connect with the Foetus” on 19th April, 2025 organized Bilaspur Obstetrics & Gynaecological Society and Society of Fetal Medicine, Chhattisgarh Chapter, Bilaspur, Chhattisgarh.
• Faculty Panelist in Panel discussion on “Reccurent Pregnancy Loss” on 13th April, 2025 at symposium entitled “Nurturing Possibilities – Creating Tomorrow” in East India Fertility Conclave – An ISAR Bengal Initiative.
• CME lecture on “Fetal medicine and genetics: The Hand and Glove” at “FetoRad – The Symposium” on 6th April, 2025 organized Department of Radiology, Shri Shankaracharya Institute of Medical Sciences, Vilai, Chhattisgarh.
• CME lecture on “Genetic Testing in Endocrinology” on 21st January, 2025 organized by Department of Endocrinology, Sir Nilratan Sircar Medical College and Hospital, Kolkata, West Bengal.
• Invited webinar lecture on “Genetics of Neuro Developmental Disorders and Emerging Diagnostic Approaches” on 10th October, 2024 organized by Progenics Laboratories Pvt. Ltd., India.
• Invited lecture on “Climbing through the DNA ladder – genomic diagnosis as career” at 10th Annual Biotech Industry Conclave 2024 at KIIT University, 24th August, 2024.
• Invited lecture on “Career in Genetics” as part of Add-on Certificate course “Career opportunities in life sciences” organized by Mahadebananda Mahavidyalaya on 27th June, 2024.
• Invited lecture on “Importance of prenatal diagnosis in detecting genetic abnormalities” at FETOMEET, Patna on 19th May, 2024
• Invited Lecture on “Genetic Diagnosis, Gene Therapy and career in Genetics” at KIIT University, Odisha, 7 November, 2023
• RTM at Rani Hospital, Ranchi, Jharkhand, on “Redefining accurate genetic diagnosis by EXOME FIRST” – 20 October, 2023
• Faculty Panelist in Panel discussion in “Nephrogenetics Workshop” at ISPNCON 2023 by Indian Society of Pediatric Nephrology, 13th October, 2023
• Faculty panelist in Panel discussion at CSIR-IGIB on “Genetic Counselling in India – Challenges and Opportunities”, 20th September, 2023
• Weekly series by CURIA on Genetic screening for cancer risk assessment, 26th July, 2023.
• ISAR Odisha chapter, CME on Precision Gyenocology Genetic Update, Panel Expert, 25th July, 2023
• Webinar by Heredity Bioscience, Bhubneswar, on “Genetic diagnosis and Future Prediction”, 21st July 2023.
• CME at Berlin Diagnostics on “Fetal Imaging Genetics”- 2nd July, 2023.
• RTM at Rani Hospital, Ranchi, Jharkhand, on “Genetic Diagnosis in Pediatrics” – 23rd March, 2023
• Faculty Panelist in Panel Discussion on “Antenatal Screening in Predicting Neo-Natal Outcome” organized by IAP Barrack Valley with NNF Assam & Silchar O & G Society, Silchar, Assam on the occasion of World Down Syndrome Day – 19th March, 2023
• Invited Lecture to IAP Barrack Valley with NNF Assam & Silchar O & G Society, Silchar, Assam on the occasion of World Down Syndrome Day, on “Newer Insights of Genetic Diagnosis in Childhood Disease” – 19th March, 2023
• Invited Lecture at Sardar Vallav bhai Panth Post Graduate Institute of Pediatrics, Cuttack, Odisha on the Occasion on World Kidney Day, 2023 on “Interpretations of NGS and Microarray” – 11th March, 2023.
• RTM at Calcutta National Medical College, Kolkata on “Genetic Testing as Diagnostic Checkpoints in Pediatrics” – 24th February, 2023.
• CME at Garden Palace Banquet Hall, Kolkata organized by LifeCell International Pvt. Ltd, on “Importance of Non-Invasive Prenatal Screening” – 18th December, 2022.
• RTM at Jagyaseni Hospital, Jharsiguda, Odisha on “Genetics behind Bringing Healthy Next Generation” – 17th December, 2022.
• RTM at Bhagirathi Neotia Women and Child Care Hospital, Newtown, Kolkata on “Utility of 5 Days Exome Sequencing in NICU and PICU” 29th November, 2022.
• RTM at Calcutta Medical College, Kolkata on “Nitty-gritties of Genetic Testing in Neurological Disorders” – 28th November, 2022
• Panel Discussion (Faculty Member) on “Genetic Testing in Paediatric Nephrology” at APNEICON, 2022, Kolkata, – 29thn & 30th October, 2022.
• RTM at R N Tagore International Institute of Cardiac Sciences, Mukundapur, Kolkata on “Importance of Next Generation Sequencing in Better Management of Rare Neurological Disorders” – 15th September, 2022.
• CME at Sumang Health Care Private Limited, Kolkata on “Reaching To The Diagnosis in Neurodevelopmental Disorders – Use of Genetic Testing” – 10th September, 2022
• CME at All India Institute of Medical Sciences, Kalyani, West Bengal on “Genetic Counselling in Inborn Errors of Metabolisms” – 27th August, 2022.
• RTM at R N Tagore International Institute of Cardiac Sciences, Mukundapur, Kolkata on “Importance of Next Generation DNA Sequencing in Early Detection and Better Management of Rare Genetic Diseases in Pediatric Set Up” – 22nd August, 2022.
• CME at STADEL, Kolkata, organized Divine Nursing Home, Kolkata on “Genetic Testing As a Solving Tool in Women And Child Health Care” – 6th August. 2022
• CME at Society for Obstetrics and Gynecology, Siliguri (SOGS) on “Genetic Testing – the Aladin’s Genie in Gynaecology and Obstetrics” – 26th June, 2022
• Participated as a panellist in a Panel Discussion on Premarital and Prenatal Genetic Screening from the eyes of Genetics and Psychology, Organised by BIO-SOC, Biotechnology Department, Delhi Technological University (DTU), 14th May 2022.
• Delivered a lecture as Guest Speaker in CME on “Rare Genetic Disorders- how genetic testing and genetic counselling can help” on 24th March 2022, Organized by Redcliff Genetics and Tata Motors Medical Hospital, Jamshedpur.
• Delivered invited lecture on “Genetics of Neurodevelopmental Disorders” in the webinar – “Autism and Neurodevelopmental Disorders – from Genetics to functional pathways” organized by Redcliffe Genetics, India on 17th February, 2022.
• Acted as resource person in UGC-HRDC Refresher Course in Life Science organized by Department of Genetics, University of Calcutta held from 25th February to 10th March, 2021.

RESEARCH EXPERIENCE

• From August 2003 to May 2009, I have worked under the supervision of Dr. Krishnadas Nandagopal at the Manovikas Biomedical Research and DiagnosticCentre in Kolkata. My dissertation research involved studying the serotonergic system genes (serotonin transporter and serotonin receptor 1B) in Attention–Deficit-Hyperactivity-Disorder (ADHD), a heritable, psychiatric disorder with onset in childhood. After genotyping ADHD patients and their families, who have been recruited from the Kolkata region of India, with regard to five polymorphisms of serotonin transporter and three polymorphisms of serotonin receptor, I have found that the STin2.12 (serotonin transporter) and C861 (serotonin receptor1B) alleles are positively associated and linked with increased risk of ADHD. Interestingly, the maternal transmission of the risk allele
is significant in both the loci. I have also found that there is significant probability of interaction is present between the two risk loci G861C (serotonin receptor1B) and STin2 (serotonin transporter).

• From January 2010 to December, 2013, I worked as a DBT-Research Associate on my project “A search for the basis of differential vulnerability of dopaminergic neurons in the ventral tegmental area and substantia nigra region in Parkinson’s disease”. the differential protein expression in the SN and VTA region of normal mice brain and MPTP treated mice brain to study
• From November 2019 to till date I am working as a Geneticist and Genetic Counsellor at MFC Woman and Child Care.

TRAININGS ACHIEVED

• Successfully completed the following modules of the online course “GENOMIC VARIANT ANALYSIS & CLINICAL INTERPRETATION” offered by CSIR-IGIB, New Delhi, India
o GVACI – Introduction to Basic Concepts
o HGVS Nomenclature of Genomic Variants
o Curation and Annotation of Genomic Variants
o ACMG/AMP Classification of Genomic Variants
• Successfully completed Certificate in Genetic Counseling (CGC), offered jointly by University of Manchester & Welcome Connecting Science, UK
• Successfully completed Certificate in Genetic Counselling (CGC) offered by IMA.
• Successfully completed hands on workshop on clinical applications of molecular cytogenetics organized by Centre for DNA Fingerprinting & Diagnostics (CDFD, Hyderabad); 10th -15th June 2019.
• Successfully completed 4 day course of hands on workshop and lectures of neurochemical research at ISN-APSN-IBRO School held at Osaka University school of medicine & NARA Institute of Science & Technology; September 25th -28th, 2012.
• Successfully completed the Open-Door workshop on Working with Human Genome Sequences, organized by Wellcome Trust; CCMB, Hyderabad (1-3 rd October 2008).
• Successfully undergone Training Program on Technology Led Entrepreneurship of HRDGCSIR at IICT, Hyderabad; 2nd
-27th June 2008.
• Successfully completed workshop on “Diagnosis of Genetic Disorders Using Cytogenetics & Molecular Genetics Methods” organized by Departments of Pediatrics, Anatomy & Hematology, All India Institute of Medical Sciences, New Delhi, April 17th
-26th, 2006.

TEACHING EXPERIENCE

• In 2017, I was appointed as Guest Faculty for taking theoretical classes of CBCC A2 (Human Genetics: Concepts and Paradigms) of Calcutta University post graduate studies, my appointment for this post was also renewed for 2018 – 19 session.
• Since2018 I am appointed as guest faculty for taking theory classes in Department of Genetics, University of Calcutta till date.
• I am also acting as paper setter and examiner for the above-mentioned courses.
• Delivered series of Seminar lectures for the M. Sc. Genetics students of University of Calcutta in 2020-2021 session.

FIELD WORK EXPERIENCE

• During my Ph. D. work, under the aegis of “Mental Retardation Awareness Programme” I went with my other colleagues of Manovikas Kendra (MRIH) to villages of 24 PGS(S) located near Sonarpur-Rajpur Panchayet area for creating awareness among local people about the mental illnesses, their symptoms and treatments.
• Also I had regularly attended the Out Patient Department of the Manovikas Kendra for taking ADHD and Downs’ Syndrome patient cases and counseling throughout my PhD tenure.

LIST OF PUBLICATIONS

• Bhattacharjee, K., Ghosh, K., Mukherjee, S., Upendram, P., Banerjee, E. et al. Genetic Counselling Report in Gynaecological Cases – How to keep it comprehensive yet easy to understand. Middle East Fertil Soc J (ACCEPTED)
• Banerjee, E., Pal, S., Biswas, A. et al. From uncertain to certain—how to proceed with variants of uncertain significance. Middle East Fertil Soc J 29, 43 (2024). https://doi.org/10.1186/s43043-024-00202-9
• Bhattacharjee, K., Pal, S., Banerjee, E., & Mukherjee, S. (2024). Recurrent Pregnancy Loss Associated Cytogenetic and Genetic Anomalies – Study from Eastern India. International Journal of Experimental Research and Review, 37(Special Vo), 85-95. https://doi.org/10.52756/ijerr.2024.v37spl.007
• Banerjee, E., Bhattacharjee, K. Genetic Counselling: the biomedical bridge between molecular diagnosis and precision treatment. Egypt J Med Hum Genet 23, 85 (2022). https://doi.org/10.1186/s43042-022-00297-7.
• Bhattacharjee K, Saha S, Banerjee E and Ganguly P. 2020. Strategic lockdown and blessing variation – potential success keys against COVID-19. Asian Journal of Medical Sciences, Vol. 11, Issue 4, Pages 9 – 19.
• Dutta D, Ali N, Banerjee E, Singh R, Naskar A, Paidi RK, Mohanakumar KP. Low Levels of Prohibitin in Substantia Nigra Makes Dopaminergic Neurons Vulnerable in Parkinson’s Disease. Mol Neurobiol. 2018 ;55(1):804-821. PMID: 28062948.
• Banerjee E, Nandagopal K. Does serotonin deficit mediate susceptibility to ADHD? Neurochem Int. 2015 Mar;82:52-68. doi: 10.1016/j.neuint.2015.02.001. Epub 2015 Feb 12. Review. PubMed PMID: 25684070.
• Emili Banerjee, Disha Banerjee, Swagata Sinha, Anindita Chatterjee, Krishnadas Nandagopal (2012), Selective maternal inheritance of risk alleles and genetic interaction between serotonin receptor-1B (5-HTR1B) and serotonin transporter (SLC6A4) in ADHD. Psychiatry Research; 200(2-3):1083-5.
• Emili Banerjee, Swagata Sinha, Anindita Chatterjee, Krishnadas Nandagopal (2009), No causal role for the G482T and G689T polymorphisms in translation regulation of serotonin transporter (SLC6A4) or association with Attention-Deficit-Hyperactivity Disorder (ADHD). Neuroscience Letters. 454: 244-248.
• Emili Banerjee, Swagata Sinha, Prasanta Kumar Gangopadhyay, Anindita Chatterjee, Manoranjan Singh and Krishnadas Nandagopal (2006) A family-based study of Indian subjects from Kolkata reveals allelic association of the Serotonin transporter intron-2 (STin2) polymorphism and Attention-Deficit-Hyperactivity disorder (ADHD). Am J Med Genet.
(Neuropsychiatric Genet.) 141B: 361-366.

PUBLISHED ABSTRACTS

• Emili Banerjee Bhattacharjee, Koutilya Bhattacharjee, Arundhati Banerjee. Few rare neurodevelopmental disorder cases from West Bengal – Genetic counselling as the diagnostic solving key. 7th Annual International Conference: BGCI 2022. 1st – 3rd July 2022.
• Koutilya Bhattacharjee, Emili Banerjee Bhattacharjee, Shiuli Mukherjee. Recurrent pregnancy loss & chromosomal aberrations – case reports from West Bengal. 7th Annual International Conference: BGCI 2022. 1st – 3rd July 2022.
• Emili Banerjee, Debashis Dutta, KP Mohanakumar. An in vivo search in the ventral tegmental area and substantia nigra region for the basis of differential vulnerability of dopaminergic neurons in Parkinson’s disease. Joint Symposium of 10th Biennial meeting of the Asia Pacific Society for Neurochemistry 55th Japanese Society for Neurochemistry. Journal of
Neurochemistry, 123, supplement 1, 102, 2012.
• Debashis Dutta , Emili Banerjee, Amit Naskar et al., Mitochondrial chaperones and sirtuin family of deacetylases: Sensitivity of dopaminergic neurons in SN vs. VTA to parkinsonian neurotoxin. Annals of Neuroscience, 19, 30, 2012.
• Debashis Dutta , Emili Banerjee, Amit Naskar et al., Vulnerability vs. susceptibility to parkinsonian pathology: Do proteins hold key in ventral tegmental area and substantia nigra?; 81st Annual Conference of Society of Biological Chemistry.
• Emili Banerjee, Debashis Dutta , Ambili Appukuttan , KP Mohanakumar. Differential protein expression in the substantia nigra and ventral tegmental area of MPTP model of Parkinson’s disease (2011). International symposium on recent trends in neurosciences & XXIX annual conference of Indian Academy of Neurosciences. A41, P152.
• Debashis Dutta D, Emili Banerjee, Ambili Appukuttan, Sangeeta Hareendran, Merina Varghese, KM Sindhu, KP Mohanakumar (2011). Differential expression of proteins in cellular and animal models of pakinsons disease. Abstracts for 23rd Biennial Meeting of ISN/ESN (International Society for Neurochemistry/ European Society for Neurochemistry).
Athens, Greece. J Neurochem. Suppl 1, 2011; 118: 142.
• Emili Banerjee, Swagata Sinha, Anindita Chatterjee, Krishnadas Nandagopal. 2008. Genes, chromosomes and disease: A380, Gene-gene interaction between SLC6A4 and 5HTR1B contributing to the risk of ADHD in Indian population. Genomic Medicine 2: 352.
• Emili Banerjee, Swagata Sinha, Anindita Chatterjee, Krishnadas Nandagopal (2008) Evidence for Distortion in Familial transmission of Serotonin Transporter Intron-2 (STin2.12) and Serotonin Receptor-1B (861C) Alleles in ADHD. XXXIII Annual Conference of the ISHG and International Symposium on Genetics Revisited: the Genomics and Proteomics Advantage,
Department of Human Genetics, Andhra University, Visakhapatnam, 11th -13th February. A: P14 pp. 61.
• Emili Banerjee, Swagata Sinha, Anindita Chatterjee, Krishnadas Nandagopal (2007) Association of Serotonin Transporter Polymorphims and Attention-Deficit-Hyperactivity Disorder (ADHD) in India. International Symposium on Advances in Neurosciences & Silver Jubilee Conference of Indian Academy of Neurosciences. Banaras Hindu University, Varanasi
November 22nd -25th , 2007. Annals of Neurosciences 14, A15 pp74.
• Emili Banerjee, Swagata Sinha, Anindita Chatterjee, and Krishnadas Nandagopal (2007) “The Serotonin Transporter G689T polymorphism in Attention-Deficit-Hypercativity Disorder (ADHD)” – Symposium on Frontiers in Biological Research organized by the Society of Biological Chemists (Kolkata Chapter), Aug 2007, Visva Bharati, Santiniketan A:15 pp.19.
• Emili Banerjee, Krishnadas Nandagopal (2007) Manually curated functional annotation of the 3’ Untranslated Region of the Human Serotonin Transporter (SLC6A4). International Sympoisum on Neurodegeneration and Neuroprotection, Indian Institute of Chemical Biology, Kolkata.
• Emili Banerjee, Swagata Sinha, Prasanta Kumar Gangopadhyay, Anindita Chatterjee, Manoranjan Singh and Krishnadas Nandagopal (2005) Characterization of Serotonin Transporter
Polymorphism in the Indian Population. Symposium on Molecular Medicine and Health, 9th ADNAT & 30th ISHG meeting, Centre for Cellular & Molecular Biology, Hyderabad A: P014
• Emili Banerjee, Swagata Sinha, Anindita Chatterjee, Prasanta Kumar Gangopadhyay, Manoranjan Singh and Krishnadas Nandagopal (2005) Evidence for Allelic Association of Serotonin Transporter Intron-2 (STin2) Polymorphism and ADHD: A Family-based Study. Symposium on Molecular Mechanism of Diseases and Drug Action (MMDDA-2005), Saha
Institute of Nuclear Physics, Kolkata A: P-08 pp.62.

TECHNICAL SKILLS

Molecular Biology:
• Human Genomic DNA isolation and quantitation by spectrophotometry
• Gel electrophoresis (2-Dimensional, Native & SDS-PAGE and agarose), silver & sypro staining; Spot cutting, Tryptic digestion and MALDI-TOF-TOF
• Polymerase Chain Reaction (PCR)
• Real time PCR
• Perfusion, Cryo-sectioning, Immunohistochemistry, Immunocytochemistry.
• Restriction Fragment Length Polymorphism (RFLP) analysis
• DNA sequencing and analysis
• Protein extraction and estimation
• Western Blotting
• TaqMan Single Nucleotide Polymorphism Genotyping Assay
• Primary cell culture, MTT assay
• Small animal behavioral assays
Cell Culture:
• SHSY5Y Neuronal cell line culture
• Human WBC primary culture for karyotyping.
Cytogenetics:
• Karyotyping from Human WBC • FISH.
Human Genetics:
• Recording family history, clinical & demographic data, maintaining database
• Chromosomal analysis by karyotyping
• Estimation of allele, gene and haplotype frequencies and linkage disequilibrium analysis
• Frequency polygon, chi-square (χ2) test and student’s t-test, ANOVA
• Transmission Disequilibrium Test, Haplotype based Haplotype Relative Risk Analysis
• Genetic power calculation,
• Multiple Dimensional Reduction analysis to detect gene-gene and gene-environment interaction
Bio-informatics:
• Use of ClustalX, Tuneclustal, BLAST, Primer-3, ReBase,
• Population Genetics Analysis software, Linkage and haplotype analysis software programmes (EH+, 2LD, JLIN, Haploview)
• QuantityOne, PDQuest (BIORAD)
• RNA secondary structure analysis by MFold
• CpG island analysis by EBI toolbox CpG Plot/CpG report, UTR scan
• Promoter prediction and transcription factor binding mapping by Genomatix software program
• SPSS
• PD quest

PROFESSIONAL MEMBERSHIPS

• Life Member of the Indian Society of Human Genetics since January 2004
• Life Member of the Calcutta Consortium On Human Genetics since March 2009.

EXTRACURRICULAR INTERESTS

I am a keen participant in elocution and classical music programs and have performed in music events conducted by All India Radio, Kolkata.

SOCIAL MEDIA ACTIVITIES

Runs an facebook page titled as “DR. Emili – Your Genetic
Guide” – https://www.facebook.com/Dr-Emili-Your-Genetic-Guide-110483464570049
• Google Business Address – https://dr-emili-banerjee-bhattacharjeeph-d-postdoc.business.site/?utm_sourcegmb&utm_mediumreferral
• Invited Talk shows o Talk show in “PRATHAMA”
https://m.facebook.com/story.php?story_fbid953552218900593&id10000077286698
4&sfnsnwiwspmo
o Talk show in “YOU MATTER” – https://fb.watch/ak-N2ATBVj/
o Talk show in BIO-LOGICS – https://www.facebook.com/110322003964310/videos/273878263702998
Talk show on genetic testing SANANDA Magazine.