Cynthia Morton

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The University of Manchester

United Kingdom

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Recent Grants

Grant: Close

SEQuencing a Baby for an Optimal Outcome (SEQaBOO)

Open Date: 2016-03-01

Close Date: 2021-02-28

Grant: Close

Genetic Studies of Uterine Leiomyomata

Open Date: 2010-07-20

Close Date: 2017-12-31

Grant: Close

Finding Genes for Uterine Fibroids

Open Date: 2003-09-26

Close Date: 2010-07-31

Grant: Close

DGAP: Developmental Genome Anatomy Project

Open Date: 2000-04-01

Close Date: 2020-03-31

Grant: Close

Cloning Genes Involved in Hearing

Open Date: 1997-08-01

Close Date: 2014-08-31

Articles (12)

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2025

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2025

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2024

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2024

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2024

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2023

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2023

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2023

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2023

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2022

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2022

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2022

Collaborators (13)

Joel Rämö

University of Helsinki

FINLAND

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Olga R Brook

Beth Israel Deaconess Medical Center

UNITED STATES

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Dezso David

Instituto Nacional de Saúde Doutor Ricardo Jorge

PORTUGAL

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Soo-Hyun Kim

Adjunct Professor

Yonsei University College of Medicine

SOUTH KOREA

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Frances Williams

King’s College London

UNITED KINGDOM

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Gonneke Willemsen

University of Amsterdam

NETHERLANDS

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Natalia Trpchevska

Karolinska Institutet

SWEDEN

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Elmo Saarentaus

University of Helsinki

FINLAND

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Nikki Hubers

University of Amsterdam

NETHERLANDS

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Maxim Freydin

Lecturer in Medical Genetics

Queen Mary University of London

UNITED KINGDOM

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Teemu Palviainen

University of Helsinki

FINLAND

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Sofia Dória

Professor

PORTUGAL

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Andries Paul Nagtegaal

NETHERLANDS

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Cynthia Morton

Research Interests

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Recent Grants

Articles (12)

2024 ASHG Leadership Award

Newborn Screening for Deafness/Hard of Hearing in the Genomic Era

Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity

Chromosomal structural rearrangements implicate long non-coding RNAs in rare germline disorders

Genetic contribution of reproductive traits to risk of uterine leiomyomata: a large-scale genome-wide cross-trait analysis

Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage

A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

A Comparative Analysis of Health-Related Quality of Life 1 Year Following Myomectomy or Uterine Artery Embolization: Findings from the COMPARE-UF Registry.

Long-term health-related quality of life and symptom severity following hysterectomy, myomectomy, or uterine artery embolization for the treatment of symptomatic uterine fibroids

Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing

Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis

Collaborators (13)

Joel Rämö

Olga R Brook

Dezso David

Soo-Hyun Kim

Frances Williams

Gonneke Willemsen

Natalia Trpchevska

Elmo Saarentaus

Nikki Hubers

Maxim Freydin

Teemu Palviainen

Sofia Dória

Andries Paul Nagtegaal

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