Since 2017 The Most Trusted Genetics Brand

Genetic Testing & Genetic Counselling in Noida

Expert cytogenetic testing and compassionate genetic counselling led by an AIIMS New Delhi alumnus with 23+ years of experience in laboratory genetics. Serving Delhi NCR and patients across India.

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AIIMS New DelhiAlumnus-led team

Karyotype · FISH · CMAExpert interpretation

25+ PublicationsPeer-reviewed research

Accurate TestingTrusted genetic solutions

Get ResultsClear, timely reporting

Secure ReportsConfidential patient data

24/7 SupportWe are here when you need us

23+Years of founder experience in laboratory genetics

About CYTOGeNeOM

Helping families understand their genes and make informed choices

Genetic counselling is a specialised healthcare service that helps individuals, couples and families understand how genetics may affect their health. We review your personal and family history, interpret genetic test results and explain how genes relate to health, disease and inheritance.

Assess the risk of inherited conditions

Explain findings and testing options clearly

Support family-planning decisions

Provide emotional support throughout

Read Our Story

Why Choose Us

Medical expertise, laboratory support and compassionate counselling

CYTOGeNeOM is devoted to reducing the burden of genetic disorders. Every patient receives personalised guidance from first consultation to final report.

Proven Expertise

PhD-level knowledge from AIIMS and 23+ years in clinical cytogenetics and genomics.

Personalised Care

Counselling tailored to your history, concerns and family goals.

End-to-End Support

From test selection and sample collection to report interpretation.

Global Best Practices

Processes aligned with ISO 15189 / NABL standards.

Led by Dr. Ashish Fauzdar

Consultant, Laboratory Genetics, Clinical Cytogenetics & Genetic Counselling

23+Years in laboratory genetics

25+Peer-reviewed publications

CAPCertified cytogenetics inspector

NABLAssessor, ISO 15189:2022

Our Approach

How genetic counselling works

A clear, five-step process so you always know what happens next.

Case Review

Detailed review of personal and family history and previous reports.

Education

Clear explanation of the condition, inheritance and testing options.

Decision Support

Help choosing tests and making informed family-planning decisions.

Psychosocial Support

Compassionate support through sensitive or complex results.

Care Integration

Coordination with your doctor, IVF clinic or care team.

Our Core Services

Genetic counselling across every stage of life

From preconception planning to oncology and adult-onset conditions, we guide you through testing and results.

Preconception & Prenatal

Carrier screening, prenatal options and support for families planning a pregnancy.

Carrier screening (thalassemia, SMA, cystic fibrosis)
Advanced parental age risk assessment
NIPT, CVS and amniocentesis guidance
Support after recurrent pregnancy loss

Paediatric & Rare Disease

Diagnostic evaluation for children with suspected genetic conditions.

Congenital malformations & developmental delay
Metabolic and neuromuscular disorders
Family testing
Clinical trial referrals

Oncology Genetics

Hereditary cancer risk assessment and family cascade testing.

Hereditary cancer risk (BRCA1/2, Lynch syndrome)
Risk-reduction counselling
Cascade testing for relatives

Adult & Predictive

Counselling and testing for adult-onset and inherited conditions.

Neurogenetic conditions (e.g. Huntington's)
Cardiogenetics (Marfan, long QT)
Pharmacogenetics
Presymptomatic testing

Haematology & Immunogenetics

Genetic evaluation for blood and immune disorders.

Haemoglobinopathies
SCID and immunodeficiencies
Transplant-related evaluation

Assisted Reproduction & IVF

Genetic support for couples undergoing fertility treatment.

PGT for aneuploidy or single-gene disorders
IVF/ICSI risk assessment
Donor gamete ethics counselling
Reproductive options for carriers

Diagnostic Tests

Advanced cytogenetic & genetic testing

Karyotyping

The gold-standard test to rule out chromosome abnormalities in number and structure.

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FISH

Fast, targeted detection of chromosomal changes, with results usually within 24 hours.

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Chromosome Microarray

High-resolution genome-wide detection of microdeletions and duplications.

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Prenatal Screening & NIPT

Screening options from 9–10 weeks, including double marker, quad test and NIPT.

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Dr. Ashish FauzdarFounder · PhD, Reproductive Genetics (AIIMS)

Meet Our Founder

Dr. Ashish Fauzdar

An AIIMS New Delhi alumnus with a doctorate in Reproductive Genetics and over 23 years of experience in laboratory genetics and genomics across academic institutions, hospitals, ART/infertility clinics and diagnostic laboratories.

CAP-certified Cytogenetics Inspector NABL Assessor, ISO 15189:2022 Board of Genetic Counselling, India Registered under PC-PNDT Act

23+Years of experience

25+Publications

4Core techniques: Karyotype, FISH, CMA, NGS

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Recognition