Fetal hydrops and the Incremental yield of Next generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis

Publication: Ultrasound in Obstetrics and Gynecology

F. Mone,  R. Y. Eberhardt, M. E. Hurles,  D. J. McMullan,  E. R. Maher,  J. Lord,  L. S. Chitty,  E. Dempsey,  T. Homfray,  J. L. Giordano,  R. J. Wapner,  L. Sun, T. N. Sparks,  M. E. Norton, M. D. Kilby

13 April 2021


Summary

Use of prenatal next generation sequencing in both isolated and non‐isolated NIHF should be considered in developing clinical pathways.

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The mutational landscape of normal human endometrial epithelium

Publication: Nature

Luiza Moore, Daniel Leongamornlert, Tim H. H. Coorens, Mathijs A. Sanders, Peter Ellis, Stefan Dentro, Kevin Dawson, Tim Butler, Raheleh Rahbari, Thomas J Mitchell, Francesco Maura, Jyoti Nangalia, Patrick S. Tarpey, Simon F. Brunner, Henry Lee-Six, Yvette Hooks, Sarah Moody, Krishnaa Mahbubani, Mercedes Jimenez-Linan, Jan J. Brosens, Christine A. Iacobuzio-Donahue, Inigo Martincorena, Kourosh Saeb-Parsy, Peter J. Campbell, Michael R. Stratton

22 April 2020


Summary: 

This paper looks at somatic mutation (changes in the DNA) in healthy human tissue in the endometrium (womb lining) and provides insights into the earliest stages of uterine cancer development, which is the fourth most common cancer in women in the UK.

Many cells in the inner lining of the uterus carry ‘cancer-driving’ mutations that frequently arise early in life. Using whole-genome sequencing to better understand the genetic changes in healthy endometrial tissue, the researchers found that a high proportion of cells carry driver mutations, even though they appear completely normal under the microscope. Furthermore the team found that many of these driver mutations appear to have arisen early in life, in many cases during childhood.

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The Manchester International Consensus Group recommendationfor the management of gynecological cancers in Lynch syndrome

Publication: Genetics Medicine

Crosbie EJ, Ryan NAJ, Arends MJ, Bosse T, Burn J, Cornes JM, Crawford R, Eccles D, Frayling IM, Ghaem-Maghami S, Hampel H, Kauff ND, Kitchener HC, Kitson SJ, Manchanda R, McMahon RFT, Monahan KJ, Menon U, Møller P, Möslein G, Rosenthal A, Sasieni P, Seif MW, Singh N, Skarrott P, Snowsill TM, Steele R, Tischkowitz M;

28 March 2019

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Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children

Publication: Intensive Care Medicine

French CE, Delon I, Dolling H, Sanchis-Juan A, Shamardina O, Mégy K, Abbs S, Austin T, Bowdin S, Branco RG, Firth H, , Rowitch DH, Raymond FL

07 March 2019

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Genomic imprinting disorders: lessons on how genome, epigenome and environment interact

Publication: Nature Reviews

Monk D, Mackay DJG, Eggermann T, Maher ER, Riccio A.

15 January 2019

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BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors

Publication: Genetics in Medicine

Lee A, Mavaddat N, Wilcox AN, Cunningham AP, Carver T, Hartley S, Babb de Villiers C, Izquierdo A, Simard J, Schmidt MK, Walter FM, Chatterjee N, Garcia-Closas M, Tischkowitz M, Pharoah P, Easton DF, Antoniou AC.

15 January 2019

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Clinical Practice Guidance: Surveillance for phaeochromocytoma and paraganglioma in paediatric succinate dehydrogenase gene mutation carriers

Publication: Clinical Endicrinology

Wong MY, Andrews KA, Challis BG, Park SM, Acerini CL, Maher ER, et al.

27 December 2018

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Factors Associated With Outcomes of Patients With Primary Sclerosing Cholangitis and Development and Validation of a Risk Scoring System

Publication: Hepatology

Goode EC, Clark AB, Mells GM, Srivastava B, Spiess K, Gelson WTH, et al.

19 December 2018

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Bone morphogenetic protein 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasia

Publication: European Journal of Human Genetics

Nixon TRW, Richards A, Towns LK, Fuller G, Abbs S, Alexander P, et al.

19 December 2018

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Pruritus is Common and Under-treated in Patients with Primary Biliary Cholangitis in the United Kingdom

Publication: Clinical Gastroenterology Hepatology

Hegade VS, Mells GF, Fisher H, Kendrick S, DiBello J, Gilchrist K, et al.

14 December 2018

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