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    Shehla Mohammed

    Clinical Lead for National Highly Specialist Service - Cockayne and Trichothiodytrophy Syndromes

    Shehla Mohammed is a highly experienced paediatric clinical geneticist with a focus on rare genetic disorders and care for children with life-limiting conditions. With 24 years in the field, she has a keen interest in paediatric neuromuscular and DNA repair disorders.

    Her educational background includes FRCP at the Royal College of Physicians, UK, Diploma in Child Health from the Royal College of Physicians, London, and MBBS with honors from the University of Punjab. She also holds a Doctor of Medicine degree and has conducted research on familial breast cancer.

    Shehla Mohammed's extensive organizational involvement includes roles such as Clinical Lead for National Highly Specialist Services at Guy's and St Thomas' NHS Foundation Trust, Programme Associate at PHG Foundation, and Consultant Clinical Geneticist at various healthcare institutions.

    She has served in various capacities within the medical field, from Paediatric Registrar to Consultant Clinical Geneticist, showcasing her diverse experience and expertise in clinical genetics, paediatrics, and research.

    In addition to her clinical roles, she has been actively involved in committees and working groups, demonstrating her commitment to advancing clinical practices and standards. She has also contributed significantly to organizations such as the UK Genetic Testing Network and NICE.

    With a solid foundation in genetics, paediatrics, and clinical research, Shehla Mohammed continues to make valuable contributions to the field of paediatric clinical genetics and rare genetic disorders.

    Shehla Mohammed
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    Location

    London, Greater London, United Kingdom