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    Academics: Curriculum Vitae of Nikhil Kasarpalkar

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    Nikhil
    Nikhil Kasarpalkar's CV summarizes his education and experience in genetics. He holds an M.Sc. in Research from CREMERE and a B.Sc. in Biotechnology. His experience includes hands-on training in techniques like karyotyping, identifying lysosomal storage disorders, and using equipment like HPTLC and GC/MS. He has worked on genetics projects studying disorders like Down syndrome, fragil X syndrome, and lysosomal storage disorders. Kasarpalkar has published and presented his research at conferences on topics related to genetic screening and disorders.

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    Academics: Curriculum Vitae of Nikhil Kasarpalkar

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    Nikhil Kasarpalkar's CV summarizes his education and experience in genetics. He holds an M.Sc. in Research from CREMERE and a B.Sc. in Biotechnology. His experience includes hands-on training in techniques like karyotyping, identifying lysosomal storage disorders, and using equipment like HPTLC and GC/MS. He has worked on genetics projects studying disorders like Down syndrome, fragil X syndrome, and lysosomal storage disorders. Kasarpalkar has published and presented his research at conferences on topics related to genetic screening and disorders.

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    Nikhil Kasarpalkar's CV summarizes his education and experience in genetics. He holds an M.Sc. in Research from CREMERE and a B.Sc. in Biotechnology. His experience includes hands-on training in techniques like karyotyping, identifying lysosomal storage disorders, and using equipment like HPTLC and GC/MS. He has worked on genetics projects studying disorders like Down syndrome, fragil X syndrome, and lysosomal storage disorders. Kasarpalkar has published and presented his research at conferences on topics related to genetic screening and disorders.

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    157 views3 pages

    Academics: Curriculum Vitae of Nikhil Kasarpalkar

    Uploaded by

    Nikhil
    Nikhil Kasarpalkar's CV summarizes his education and experience in genetics. He holds an M.Sc. in Research from CREMERE and a B.Sc. in Biotechnology. His experience includes hands-on training in techniques like karyotyping, identifying lysosomal storage disorders, and using equipment like HPTLC and GC/MS. He has worked on genetics projects studying disorders like Down syndrome, fragil X syndrome, and lysosomal storage disorders. Kasarpalkar has published and presented his research at conferences on topics related to genetic screening and disorders.

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    Curriculum Vitae of Nikhil Kasarpalkar

    Name- Nikhil Kasarpalkar


    Date of Birth- 23/02/1986
    Add: A/4, Ganga Apts,
    Nr Kamal Sagar Soc.
    90 Feet Rd, Bhandup(E).
    Mumbai 400042
    Contact No-+ 919769692895
    e-mail- nikhil_mi2@hotmail.com

    Academics
    Degree Institution Class Year
    M.Sc.( By Research) Centre For Research In Current Current
    Mental Retardation(CREMERE)
    B.Sc in Biotechnology Vikas College of Arts, First Class April-2006
    Science and Commerce
    HSC K.J Somaiya College Of First Class March, 2003
    Science and Commerce
    SSC Indian Education Society’s Distinction March, 2001
    Secondary School

    Courses Completed
    Post Graduate Diploma In Bioinformatics (2003-04)- Vikas Career College in association
    with Indian Bioinformatics Organisation. Grade A+.

    Hands on Experience
    1) Hands on experience and Training in cytogenetics. Well versed in the technique of
    separation and identification of chromosomes(Karyotyping) through G-banding.

    2) Through understanding and training in the isolation, separation and identification of


    Lysosomal Storage Disorders (LSDs) through Leucocytes

    3) Have handled cases of biotinidase deficiency and multiple carboxylase deficiency.


    with a fine understanding relating to the its literature and the technique of its detection
    4) Training in high risk prenatal screening in the first and second trimester of pregnancy with
    the DELFIA system. Well versed in handling the assays for the related markes of free β-
    hcg, PAPP-A for the first trimester and free β-hcg, AFP and UE3 in the second trimester

    5) Training in handling the High Performance Thin Layer Chromatogarph (HPTLC)used in


    the separation of serum amino-acids which are useful of diagnosis of certain metabolic
    disorders

    6) Training in the handling of the Gas Chromatography Mass Spectrometry (GC/MS)for


    diagnosis of many Metabolic Disorders

    7) Have a through understanding of the techniques to lucratively process molecular DNA


    Samples

    8) Standardisation & developing lysosomal enzyme testing for 14 lysosomal disorders by


    spectrophotometry & flurometry ( ICMR project study )

    Experience In Genetics
    1) Well versed in the history taking of genetic disorders related to Mental Retardation with
    regards to the proper handling and through detailing of the concerned patients related to
    Down Syndrome, Autism, Fragile X Syndrome and other genetic disorders.
    2) An experience of over 3 years in cytogenetics, metabolic genetics, genetic history
    taking, biochemical genetics, molecular genetics and genetic counseling.
    3) Have worked as a assistant fellow in the ICMR project for the screening and diagnosis
    of lysosomal storage disorders under the guidance of Dr. Usha P. Dave-Medical
    geneticist.
    4) Have worked for 1 year as a Junior Research Fellow at Preventine Life Care, Mumbai.
    5) Experience of organizing and successfully conducting workshops, CMEs, and seminars
    on Clinical Genetics , Genetic counselin and Genetic disorders
    6) Trained in taking lectures and practical related to basics of genetics, metabolic genetics,
    inborn errors of metabolism, cytogenetics & mental retardation

    Publications and Presentations


    1. Kasarpalkar N, Arora M and Dave U (2008) “Is advanced maternal age a
    criteria for screening Indian pregnant women?- chromosomal profile in 280 down
    syndromes ” presented at International conference On Medical And Community
    Genetics
    2. Kasarpalkar N, Sanghi V, Kavimandan B and Dave U (2009). “A Spectrum of
    Arylsulfatase- A Deficiency (MLD) – a rare neurodegenerative disorder” presented at the
    7th Annual Conference of Bombay Neurosciences Association ( BNA )
    Prizes
    First prize in the Event of Srujan -2005 organised by Smt. C.H.M College,
    Ulhasnagar for the project titled “Pseudogenes and Bioinformatics”

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