Genetic Consultation Service in London and the UK

Schell Genetics is a Genetic Consultation Service in London and the UK. Our service is availabe on-line and in-person.

At Schell Genetics, we offer individualised evaluations, genetic consultation, and testing. Our clinical services include reproductive and prenatal counseling, carrier testing, and complete genetic evaluations for children and adults.

Our goal is to provide you with genetic information that presents choices and minimises uncertainty, empowering you to make decisions that are most beneficial for you.

Although we offer specific recommendations about your medical care, we encourage you to make reproductive and other choices that are appropriate for you based on your cultural background and personal experience.

All services are available in English and German.

What we offer

Paediatric Genetics
Answering questions on childhood genetic disorders
Cancer Genetics
Answering questions on cancer genetics
Neurogenetics
Answering questions on neurological genetic disorders
Fertility Genetics
In Reproductive Genetics we emphasise on the fertility journey of couples
Other Genetic Issues
Of course, we are committed to answer all genetic questions you might have
Healthcare Specialists
Our service for Healthcare Professionals

Who we are

Dr Chayim Schell-Apacik
Consultant Clinical Geneticist

I am happy to assist you with all questions you might have on genetic issues depending on your clinical symptoms, your family history, and previous medical findings. Genetic diagnostics and testing will not be performed without your consent. It is your decision to make and completely up to you whether to go ahead with the proposed genetic testing after the consultation.

Learn more about Dr Schell-Apacik

Why might someone have a genetic consultation?

Individuals or families who are concerned about an inherited condition may benefit from a genetic consultation. The reasons that a person might be referred to a genetic counselor, medical geneticist, or other genetics professional include:

  • A personal or family history of a genetic condition, birth defect, chromosomal disorder, or hereditary cancer.
  • Two or more pregnancy losses (miscarriages), a stillbirth, or a baby who died.
  • A child with a known inherited disorder, a birth defect, intellectual disability, or developmental delay.
  • A woman who is pregnant or plans to become pregnant at or after age 35. (Some chromosomal disorders occur more frequently in children born to older women.)
  • Abnormal test results that suggest a genetic or chromosomal condition.
  • An increased risk of developing or passing on a particular genetic disorder on the basis of a person’s ethnic background.
  • People related by blood (for example, cousins) who plan to have children together. (A child whose parents are related may be at an increased risk of inheriting certain genetic disorders.)
  • A person received results from direct-to-consumer genetic testing and they want to discuss the implications of the results.

A genetic consultation is also an important part of the decision-making process for genetic testing. A consultation with Dr Schell-Apacik may be helpful even if testing is not available for a specific condition, however.

Professional Organisations we are proud members of

General Medical Council

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