Fertility Genomics

Leveraging genomics insights to address infertility, improve reproductive outcomes, support patient specific tailored interventions, enhance success rates of ART.

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Innovation in Fertility
Innovative Fertility Testing
GeneTech leads with Genomic Fertility Analysis (GeneFeminaTM, GeneAndroTM) and advanced HLA compatibility assessments for precise fertility solutions.
Advanced Embryo Testing
Novel embryo testing methods empower IVF specialists with cutting-edge tools.
AI-Driven Personalization
Data-driven AI provides tailored recommendations to enhance fertility outcomes.
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Genetech Expertise
Our expertise in the field of Fertility Medicine includes Reproductive Genomics, Clinical Genetics, Immunogenetics, Molecular Genetics, Prenatal and Pre-implantation Genetics, Cytogenetics, Biochemical Genetics, Epigenetics and Genetic Counselling.
Experience
Handled more than 100,000+ infertility cases since 1998.
Embryo Testing
Expertise in embryo testing: Handled thousands of embryos for PGTA, PGTM or NICS.
Innovation
World’s first launch of Genomic Fertility Analysis with successful adoption by IVF clinics across the country.
Recognition
Multiple research papers on infertility in reputed international scientific journals.
Comprehensive services
Offers most comprehensive services for Fertility clinics.
GeneAndro & GeneFemina For Sucessfull IVF Pregnancy

The comprehensive female and male Genomic Fertility Analysis offers the best possible diagnostic yield through identification of genomic root cause for multiple infertility phenotypes. Provides pharmacogenomic insights and paves way for personalised treatment, leading to enhanced success rate with ART.

Learn more

Talk to your IVF Physician about GeneAndro and GeneFemina

More than 100 IVF clinics across India and overseas routinely use GeneFemina and GeneAndro in their IVF practice, and more than 10,000 couples have benefited from these in the last few years. 



Talk to your IVF physician about this.

Services
Most comprehensive genetic services for infertility - Karyotyping, GeneFeminaTM,  GeneAndroTM, HLA-sharing, AZF, CFTR, Fragile X, Carrier tests, CMA, NIPT, PGT-A, PGT-SR, PGT-M & other molecular tests.
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Los Angeles
Miami
Seattle
Genetic Counseling
Our genetic counselling services empower patients and families by providing expert guidance on genetic conditi
2 weeks
750
Book now
GeneFeminaTM
360 degree coverage of all genetic conditions associated with female infertility, premature ovarian insufficie
2 weeks
20000
Book now
HLA Sharing in Couple
High resolution HLA sharing in couple to identify maternal immune response risk caused due to sharing of HLA a
2 weeks
24000
Book now
KIR Genotyping
Maternal KIR (Killer cell immunoglobulin-like receptor) genotyping is a test to analyze a woman's genes, which
2 weeks
12000
Book now
Factor-V Leiden Mutation
The Factor V Leiden mutation is associated with increased risk of pregnancy loss, particularly recurrent misca
2 weeks
4500
Book now
Genetic Counseling
Our genetic counselling services empower patients and families by providing expert guidance on genetic conditi
2 weeks
750
Book now
Fragile X Methylation
Fragile X syndrome causes moderate to severe intellectual disability. It mostly affects males and females usua
2 weeks
10000
Book now
Fragile X Screening
Fragile X syndrome causes moderate to severe intellectual disability. It mostly affects males and females usua
2 weeks
12000
Book now
Genetic Counseling
Our genetic counselling services empower patients and families by providing expert guidance on genetic conditi
2 weeks
750
Book now
Non Invasive Chromosomal Screening (NICS) 4 Embryos
Non invasive chromosomal screening is done to identify chromosomal aneuploidy in the embryos using spent media
2 weeks
60000
Book now
Non Invasive Chromosomal Screening (NICS) 2 Embryos
Non invasive chromosomal screening is done to identify chromosomal aneuploidy in the embryos using spent media
2 weeks
30000
Book now
Non Invasive Chromosomal Screening (NICS) 3 Embryos
Non invasive chromosomal screening is done to identify chromosomal aneuploidy in the embryos using spent media
2 weeks
45000
Book now
Alpha Thalassemia Carrier Screening (for COUPLE)
Alpha Thalassemia is caused by impaired production of Alpha globin which is a part of hemoglobin molecule. The
2 weeks
30000
Book now
BRCA 1&2 Full Gene Sequencing
Hereditary breast and ovarian cancer (HBOC) risk is elevated in the presence of brca1 and 2 pathogenic gene va
2 weeks
18000
Book now
Beta Thalassemia Carrier Screening (for COUPLE)
Beta Thalassemia is caused by reduced or absent synthesis of the beta chains of hemoglobin that result severe
2 weeks
30000
Book now
Beta Thalassemia
Beta Thalassemia is caused by reduced or absent synthesis of the beta chains of hemoglobin that result severe
2 weeks
15000
Book now
Explore all tests
Fertility

Genomics

Leveraging genomics insights to address infertility, improve reproductive outcomes, support patient specific tailored interventions, enhance success rates of ART.

Book Counselling
Fertility

Genomics

Leveraging genomics insights to address infertility, improve reproductive outcomes, support patient specific tailored interventions, enhance success rates of ART.

Book Counselling

Innovation in Fertility

GeneTech remains at the forefront of fertility genomics with major breakthroughs including Genomic Fertility Analysis (GeneFemina, GeneAndro), enhanced HLA compatibility assessments, data driven AI for personalised recommendations, novel embryo testing methods that empower IVF specialists.

Book Counselling
Genetech Expertise
Our expertise in the field of Fertility Medicine includes Reproductive Genomics, Clinical Genetics, Immunogenetics, Molecular Genetics, Prenatal and Pre-implantation Genetics, Cytogenetics, Biochemical Genetics, Epigenetics and Genetic Counselling.
Experience
Handled more than 100,000+ infertility cases since 1998.
Embryo Testing
Expertise in embryo testing: Handled thousands of embryos for PGTA, PGTM or NICS.
Innovation
World’s first launch of Genomic Fertility Analysis with successful adoption by IVF clinics across the country.
Recognition
Multiple research papers on infertility in reputed international scientific journals.
Comprehensive services
Offers most comprehensive services for Fertility clinics.

GeneAndro and GeneFemina for Successful IVF Pregnancy

The comprehensive female and male Genomic Fertility Analysis offers the best possible diagnostic yield through identification of genomic root cause for multiple infertility phenotypes. Provides pharmacogenomic insights and paves way for personalised treatment, leading to enhanced success rate with ART.

Learn more

Talk to your Physician about GeneAndro and GeneFemina

The continuous and increasing adoption of GeneFemina and GeneAndro tests is a testimonial for the new standards set by GeneTech and its commitment to the field of Fertility Genomics.

More than 100 IVF clinics across India and overseas routinely use GeneFemina and GeneAndro in their IVF practice, and more than 10,000 couples have benefited from these in the last few years. 



Talk to your IVF physician about this.

Services
GeneTech is a pioneer in Fertility genetics and genomics offering services to Fertility clinics since 1998. GeneTech’s latest innovations in Fertility Genomics have transformed Fertility Medicine as a practice.
Genomic Fertility Analysis
Pre - Implantation Genetic Testing
Other Infertility Genetic tests
Family History Related
Genetic Counseling
Our genetic counselling services empower patients and families by providing expert guidance on genetic conditions, their risks, and inheritance patterns. Our counsellors assess family medical histories to identify potential genetic risks and explain the benefits and limitations of genetic testing.
750
2 weeks
Book now
GeneFeminaTM
360 degree coverage of all genetic conditions associated with female infertility, premature ovarian insufficiency, poor response to controlled ovarian stimulation, poor oocyte quality, fertillization failure, oocute maturation defects, implantation failure, failed IUI, IVF, ICSI, recurrent pregnancy losses. More than 500 genes sequenced and analyed. ART implications, preventive management, pharmacogenomic implications are provided to facilitate patient specific individualised stimulation and treatment. Research shows improvement in IVF sucess rate based on individualised treatment based on GeneFeminaTM results
20000
2 weeks
Book now
HLA Sharing in Couple
High resolution HLA sharing in couple to identify maternal immune response risk caused due to sharing of HLA alleles
24000
2 weeks
Book now
KIR Genotyping
Maternal KIR (Killer cell immunoglobulin-like receptor) genotyping is a test to analyze a woman's genes, which helps determine the compatibility between her immune cells and the fetus's cells.
12000
2 weeks
Book now
Genetic Counseling
Our genetic counselling services empower patients and families by providing expert guidance on genetic conditions, their risks, and inheritance patterns. Our counsellors assess family medical histories to identify potential genetic risks and explain the benefits and limitations of genetic testing.
750
2 weeks
Book now
Non Invasive Chromosomal Screening (NICS) 5 Embryos
Non invasive chromosomal screening is done to identify chromosomal aneuploidy in the embryos using spent media samples (5 samples) sent to the lab. It is offered to infertility patients with increased maternal age, history of recurrent pregnancy loss, recurrent IVF failures. Embryo transfer recommendations are provided along with priority score.
75000
2 weeks
Book now
Non Invasive Chromosomal Screening (NICS) 2 Embryos
Non invasive chromosomal screening is done to identify chromosomal aneuploidy in the embryos using spent media samples (2 samples) sent to the lab. It is offered to infertility patients with increased maternal age, history of recurrent pregnancy loss, recurrent IVF failures. Embryo transfer recommendations are provided along with priority score.
30000
2 weeks
Book now
Non Invasive Chromosomal Screening (NICS) 3 Embryos
Non invasive chromosomal screening is done to identify chromosomal aneuploidy in the embryos using spent media samples (3 samples) sent to the lab. It is offered to infertility patients with increased maternal age, history of recurrent pregnancy loss, recurrent IVF failures. Embryo transfer recommendations are provided along with priority score.
45000
2 weeks
Book now
Non Invasive Chromosomal Screening (NICS) 1 Embryo
Non invasive chromosomal screening is done to identify chromosomal aneuploidy in the embryo using spent media sample (1 sample) sent to the lab. It is offered to infertility patients with increased maternal age, history of recurrent pregnancy loss, recurrent IVF failures. Embryo transfer recommendations are provided along with priority score.
15000
2 weeks
Book now
Non Invasive Chromosomal Screening (NICS) 4 Embryos
Non invasive chromosomal screening is done to identify chromosomal aneuploidy in the embryos using spent media samples (4 samples) sent to the lab. It is offered to infertility patients with increased maternal age, history of recurrent pregnancy loss, recurrent IVF failures. Embryo transfer recommendations are provided along with priority score.
60000
2 weeks
Book now
Factor-V Leiden Mutation
The Factor V Leiden mutation is associated with increased risk of pregnancy loss, particularly recurrent miscarriages and late-term pregnancy loss. The mutation can lead to an increased risk of blood clots, which may result in placental complications and fetal loss. Testing followed by management options may be considered in high risk patients.
4500
2 weeks
Book now
Genetic Counseling
Our genetic counselling services empower patients and families by providing expert guidance on genetic conditions, their risks, and inheritance patterns. Our counsellors assess family medical histories to identify potential genetic risks and explain the benefits and limitations of genetic testing.
750
2 weeks
Book now
Fragile X Screening
Fragile X syndrome causes moderate to severe intellectual disability. It mostly affects males and females usually have milder symptoms. The test determines the number of CGG repeats in FMR1 gene to diagnose the Fragile X syndrome phenotype or carrier status. Female carriers may exhibit premature ovarian insufficiency.
12000
2 weeks
Book now
Fragile X Methylation
Fragile X syndrome causes moderate to severe intellectual disability. It mostly affects males and females usually have milder symptoms. The test determines methylation in FMR1 gene to diagnose the Fragile X syndrome phenotype or carrier status. Female carriers may exhibit premature ovarian insufficiency.
10000
2 weeks
Book now
HLA Sharing in Couple
High resolution HLA sharing in couple to identify maternal immune response risk caused due to sharing of HLA alleles
24000
2 weeks
Book now
KIR Genotyping
Maternal KIR (Killer cell immunoglobulin-like receptor) genotyping is a test to analyze a woman's genes, which helps determine the compatibility between her immune cells and the fetus's cells.
12000
2 weeks
Book now
Alpha Thalassemia Carrier Screening (for COUPLE)
Alpha Thalassemia is caused by impaired production of Alpha globin which is a part of hemoglobin molecule. The severe type is known as hemoglobin Bart hydrops fetalis syndrome, which is also called Hb Bart syndrome or alpha thalassemia major. The milder form is called HbH disease. The test identifies pathogenic variants of HBA1 and HBA2 genes associated with Alpha Thalassemia phenotype or carrier status
30000
2 weeks
Book now
BRCA 1&2 Full Gene Sequencing
Hereditary breast and ovarian cancer (HBOC) risk is elevated in the presence of brca1 and 2 pathogenic gene variants
18000
2 weeks
Book now
Beta Thalassemia Carrier Screening (for COUPLE)
Beta Thalassemia is caused by reduced or absent synthesis of the beta chains of hemoglobin that result severe anemia. The test identifies pathogenic variants of beta Globin gene associated with betaThalassemia phenotype or carrier status
30000
2 weeks
Book now
Beta Thalassemia
Beta Thalassemia is caused by reduced or absent synthesis of the beta chains of hemoglobin that result severe anemia. The test identifies pathogenic variants of beta Globin gene associated with betaThalassemia phenotype or carrier status
15000
2 weeks
Book now
Beta Thalassemia Carrier Screening
Beta Thalassemia is caused by reduced or absent synthesis of the beta chains of hemoglobin that result severe anemia. The test identifies pathogenic variants of beta Globin gene associated with betaThalassemia phenotype or carrier status
15000
2 weeks
Book now
Comprehensive Inherited Cancer Gene Panel
Inherited germ line mutations play an important role in cancer risk or predisposition. The test uses next-generation sequencing (NGS) based exome sequencing to analysis hereditary mutations on hundreds of genes that will help in taking preventive measures to reduce the likelihood of developing cancer.
26000
2 weeks
Book now
Explore all tests
Patient Stories
Patient Stories

Recurrent pregnancy losses

Recurrent pregnancy loss risk identified by GeneRPLTM helped couple identify that it is thrombophilia related, and also helped in therapeutic management to prevent subsequent pregnancy loss and fetal anomalies.

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Patient Stories
Patient Stories

GFA report

In agrigenomics, data analysis is vital for processing vast datasets from sequencing, uncovering genetic markers for traits like yield and resilience. It facilitates precise marker-assisted breeding, reducing time and costs while enhancing crop sustainability. Effective data analysis empowers researchers to make informed decisions, driving agricultural innovation and faster go-to-market timeframes. Stanome excels in simplifying bioinformatics..

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Patient Stories
Patient Stories

Male infertility issues

Semen analysis of the male partner showed low sperm motility and poor sperm morphology. Multiple IUI procedures did not help. Couple were contemplating whether to go for ICSI, and if yes, with self or donor sperm. GeneAndroTManalysis not only identified the root cause of male infertility but also helped them in decision making.

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Patient Stories
Patient Stories

Advancements in Genetic Diagnostics

In agrigenomics, data analysis is vital for processing vast datasets from sequencing, uncovering genetic markers for traits like yield and resilience. It facilitates precise marker-assisted breeding, reducing time and costs while enhancing crop sustainability. Effective data analysis empowers researchers to make informed decisions, driving agricultural innovation and faster go-to-market timeframes. Stanome excels in simplifying bioinformatics..

Read more
Genetics Expert 

Counselling
GeneTech pioneered genetic testing in India in 1998 and has the most comprehensive range of tests using technologies like Next Generation Sequencing (NGS), Sanger Sequencing, MLPA, Cyto Microarray, SNP arrays, qPCR, PCR, Cytogenetics, FISH, Chemiluminescence, and others.
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Testimonials
Testimonials from our highly satisfied customers, physicians, patients and research partners in diverse fields highlighting the trust and credibility built over years.
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Many of my patients with unexpected poor response in IVF, Recurrent implantation failure , Recurrent pregnancy loss have benefited from genomic fertility analysis. It has helped me a lot in taking crucial decisions, planning my treatment protocols and counseling such patients...Dr Anuradha is very approachable and always available to discuss the results.
Dr. Aradhya Achuri
MBBS, MS (ObGyn) Infertility specialist, Reproductive endocrinologist, Apollo Fertility, Hyderabad
Genetech has been doing exemplary service in the field of genetics. My patients always return happy and satisfied after attending genetic counseling at GeneTech. Experts at GeneTech are thorough professionals and help us understand latest developments in genetics. I think we gynaecologists should be utilizing their services extensively to help couples produce healthy children - Dr. Kameswari K, Senior Gynecologist, Sai Anurag Hospital, Hyderabad
Dr. K. Kameswari
MBBS, MD (ObGyn) Sai Anurag Hospital, Hyderabad
Dr. Anuradha Udumudi from GeneTech is a brilliant and committed scientist with tremendous command over medical genetics. With her knowledge and dedication, she had made original contribution to research and diagnostics in the area of infertility and reproductive medicine.
Dr. Firuza Parekh
MBBS, MD (ObGyn) DGO, FCPS Infertility Specialist, FertilTree-Jaslok, Mumbai
Swapna Health Care has been associated with Genetech since a few decades, for all the investigations related to Genetics.They are highly professional, efficient and punctual, and believe in constant updating and upgrading just like us. I am sure our journey together over the decades has benefited many patients. I wish them all the best!
Dr. Savitha Devi
Senior Obstetrician Swapna Hospital and IVF center, Hyderabad
Genomics fertility analysis allows us to look deep into the genomics and identifies the root cause of infertility and recurrent pregnancy losses. I am now not only able to answer the question “why did this happen” to my patients but I am in a position to guide them better. I congratulate Dr. Anuradha and her team for her passionate and sincere work in this field.
Dr. Vandana Hegde
MBBS, MS (ObGyn) Infertility Specialist, Reproductive Endocrinologist, Hegde Fertility, Hyderabad
GeneTech is not only a pioneer of medical genetic testing in the country, but continues to bring the most advanced technologies in helping our practice with diagnosis and management. Our association with GeneTech and Dr. Anuradha Udumudi is for more than two decades. Their service orientation and deep involvement in each and every case helps us give our best to and every patient who needs such services.
Dr. Meena Ugale
MBBS, MD (ObGyn) Kirloskar Hospital, Hyderabad
I have known Dr. Anuradha and GeneTech for more than 20 yrs. She has always been on cutting edge of genetics and always made innovations to help Indian women and thier families. She has customised what is available globally, to suit our requirements. She is always available on phone. Ask a question -- this is the problem I have, is there a genetic element to it, can anything be done? -- I always would get a solution or a way out.
Dr. V. Padmaja
MBBS, MD (ObGyn) Dr. Padmaja IVF Clinic, Vijayawada
GeneAndro test designed by GeneTech, is able to give us an idea of genetic causes for male infertility in patients where conventional reports like karotyping or Y chromosome micro deletions are normal. With the help of GeneAndro, we are not only able to identify root cause in most of our male infertility patients, we are also now able to confidently counsel our patients towards patient tailored treatment options.
Dr. Karthikeyan
MBBs, MS (Gen Sur), MCH (URO), MRCS Andrologist, Apollo Fertility, Chennai
see many patients with recurrent implantation failure and pregnancy loss. Apart from routine screening tests, I use Genomic Fertility Analysis. 100s of genes associated with infertility are sequenced & interpreted. It’s interesting how many couples have single gene defects and how well they are picked up in these genomic panels. Knowing the root genetic cause helps me manage the case and plan my treatment protocols better. The results are very useful in counseling couples.
Dr. Narmada Katkam
MBBS, MD (ObGyn), FRCOG (UK) Infertility Specialist, Genesis Fertility, Hyderabad
Genomic panels developed for infertility, recurrent pregnancy losses and PCOS are able to identify root cause for the conditions like never before. The panels are useful in making critical decisions for patients and families looking forward to have a successful fertility treatment outcome. Adopting the innovative genomic panels will help physicians a great deal specially in treating idiopathic cases. My best wishes to the team and I wish them success.
Dr. Jagdip Shah
MBBS, MD (ObGyn) Infertility specialist, Parakh Hospital, Mumbai
For a physician, it is very frustrating when we are unable to give reasons for reproductive failures. Genomic panels come very handy as they are very comprehensive and check large number of genes. Not only the results explain the underlying cause for the medical condition but also give management guidance which is very useful in my practice. Patients today want to understand the cause and are happy to follow recommendations to achieve fertility
Urvashi Sehgal
MBBS, MD (ObGyn) Infertility Specialist and ObGyn, Phoenix Hospitals, New Delhi
GeneTech's GeneAndro and GeneFemina are harbingers of the arrival of precision medicine to fertility medicine. I am proud to be an early adopter of this technology, diagnosing risks, modulating treatment protocols based on world’s first comprehensive genomic fertility analysis.
Dr. Nandita Palshetkar
MBBS, MD (ObGyn), FRCOG
Publications
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GeneTech consistently publishes research findings, case reports and review articles in reputed peer reviewed international and national journals, chapters in medical books and ART manuals, society magazines and newspapers.
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HealthBiz Insight Cover

HealthBIz Insight May 2017 issue, Diagnostics special edition covered industrial trends.

Pharmacogenomics – Inherited thrombophilia

Original article Genetic markers for inherited thrombophilia in Indian Population in the Journal of Maternal and Fetal Medicine, 2022.

Pharmacogenomics – Male infertility

Case Report on Favourable outcome with r-FSH treatment and FSHR gene variant in Fertility Science and Research 2021.

Evidence for Improved ART Success

Original article Improved ART success with GeneFemina in Fertility Science and Research 2023

Genetic Counselling for PGT-M

Review article on Genetic Counseling for PGT-M in Frotiers of Reproductive Healthcare 2023.

PGT-M for ART

Chapter on PGT-M in the book Manual of Assisted Reproductive Technologies and Laboratory Sciences- 2nd Edition 2025.

JHRS Original Article

Chapter on Response to Controlled Ovarian Stimulation and Genetic associations in Indian women in JHRS 2023 .

PGT for Clinicians

Chapter on PGT in ART in the book Fertility Update 2024

Personalised ART

Chapter on Genomic Fertility Analysis for personalised ART in the book Manual of Assisted reproductive Technologies and Laboratory (2025).

OncoFertility in clinical practice

Chapter on Cancer Genetics in in the book Oncofertility-clinical Practice and Implementation Challenges 2025
News & Events
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Latest guest lectures, panel discussions, event participation, community engagement in healthcare genomics, awards and accreditations and research developments in other fields.
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Reproductive Health Master class

On Demand Webinar: Reproductive Health Master class organised by Thermofisher.

YourGene KOL meeting 2023

Lecture at Key opinion leaders meeting organised by YourGene and Thermofisher on Non-Invasive Prenatal Testing (NIPT).

MOU with London IVF

London IVF entered into an agreement with GeneTech to offer personalised fertility treatment to patients using GeneTech’s specialised genetic services.

HOPE hospital CME 2023

Lecture to pediatricians and neonatologists of Latest advancements in genetic technologies and application in

EndoFertility 2023

Panel discussion on Recurrent pregnancy loss: Connecting dots between endocrinology and genetics at Concepts to

Maatrika 2023

Genetics of Recurrent pregnancy loss: A lecture by Dr. Anuradha Udumudi at Maatrika 2023.

MSART 2023 Malaysia

Distinguished international speaker at the annual conference of Malaysian Society of Assisted Reproductive Technology

FERTIVISION 2022

Participated by putting up a stall at IFS national conference in Hyderabad visited by more than 500 infertility specialists.

Participation in TCOG Conference

Participated by putting up a stall, delivering a lecture and participation in multiple panel discussions

Key Note Address ISOPARB

Key Note Adress by Dr. Anuradha Udumudi at 40th annual national conference ISOPARB at NRI Medical College, Vijayawada on 16th Feb 2025.

Yuva Isar 2025

Invited speaker at Genetics Workshop at YUVA ISAR 2025 conference in Chennai on 13th June 2025.

Chief Guest 9M CME

Guest lecture by Dr. Anuradha Udumudi on Genomic analysis and Pregnancy management for ObGyn at CME organised by 9M Fertility in Hyderabad.
Videos
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GeneTech produces educational videos for benefit of patients and physicians. Here are some of such videos. Also included are videos delivered by our founder at various national and international events.
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Effects of Close Relative Marriages on Offspring

Dr. Anuradha Udumudi explains effects of close relative marriages and prevention of genetic disorders in children in an interview for Bhava

Infertility Genetic tests and Personalised treatment

Dr. Anuradha Udumudi explains infertility management by genegenetic tests in an interview for BhavaniHD channel

Genetic Counseling – Commentary by GeneTech medical genetics team

Elaborate explanation of genetic counselling for different variety of cases

Genetics of Autism

Genetic basis of Autism and ADHD

What is a genetic Disorder?

All about genetic disorders, diagnosis and prevention

Carrier Screening for Couple

Carrier Screening for couple and prevention of genetic disorders in children.

Prenatal Sampling for Genetic Diagnosis

Know more about prenatal sampling procedures during pregnancy like Amniocentesis and CVS biopsy.

Evidence based treatment for infertility

Root-cause genetic diagnosis, and evidence based personalised treatment using GeneFeminaTM and GeneAndroTM

Reproductive Health Talk

Genomic technological developments and transformation of genetic diagnosis and management of reproductive health

Genetic Counselling – An overview

An overview of Genetic Counselling explained by Dr. Anuradha Udumudi detailing benefits to families seeking advice and help.
Customer Stories
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Discover how genomics testing empowers our clients in medical, agricultural, and animal sectors. From finding root cause of infertility to enhancing crop yields, explore the real-world impact of our innovative services.

Mindful Eating Practices for Better Health

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down.

Nutrition Tips for Growing Children

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down..

The Importance of Preventive Health Care

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down..

Healthy Snacking Options for Busy Lives

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down..

The Role of Hydration in Health

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down..

Effective Stress Management Techniques

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down..

The Importance of Sleep for Health

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down..

Understanding Mental Health Awareness

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down..

The Benefits of Regular Exercise

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down..

Healthy Eating Tips for a Balanced Diet

Mindful eating involves paying attention to the experience of eating and drinking. It encourages individuals to slow down..

Frequently asked questions

IVF Success: The Role of GeneAndro and GeneFemina
Enhancing IVF Outcomes: GeneAndro and GeneFemina Explained
Unlocking IVF Potential with GeneAndro and GeneFemina
Achieving IVF Success: Insights on GeneAndro and GeneFemina
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GeneTech is India’s leading genetics testing laboratory with the most comprehensive directory of genetic tests. We were established in Hyderabad in 1998, and have operations all over India.
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