Publications by authors named "Nasaim Khan"

11Publications

The introduction of risk stratified screening into the NHS breast screening Programme: views from British-Pakistani women.

BMC Cancer 2020 May 20;20(1):452. Epub 2020 May 20.

Nightingale & Prevent Breast Cancer Research Unit, Manchester University NHS Foundation Trust (MFT), Southmoor Road, Wythenshawe, Manchester, M23 9LT, UK.

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http://dx.doi.org/10.1186/s12885-020-06959-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240981PMC
May 2020

Engagement barriers and service inequities in the NHS Breast Screening Programme: Views from British-Pakistani women.

J Med Screen 2020 Sep 2;27(3):130-137. Epub 2019 Dec 2.

Nightingale & Prevent Breast Cancer Research Unit, Manchester University NHS Foundation Trust (MFT), Manchester, UK.

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http://dx.doi.org/10.1177/0969141319887405DOI Listing
September 2020

Inclusion of diverse populations in genomic research and health services: Genomix workshop report.

J Community Genet 2017 Oct 28;8(4):267-273. Epub 2017 Jul 28.

Division of Primary Care, University of Nottingham, 13th Floor, Tower Building, University Park, Nottingham, NG7 2RD, UK.

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http://dx.doi.org/10.1007/s12687-017-0317-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614885PMC
October 2017

Community engagement and education: addressing the needs of South Asian families with genetic disorders.

J Community Genet 2016 Oct 10;7(4):317-323. Epub 2016 Sep 10.

Genomic medicine, St. Mary's Hospital, Manchester Academic Health Science Centre, Central Manchester University Hospitals NHS Foundation Trust, Manchester, M13 9WL, UK.

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http://dx.doi.org/10.1007/s12687-016-0278-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138164PMC
October 2016

Role of reverse phenotyping in interpretation of next generation sequencing data and a review of INPP5E related disorders.

Eur J Paediatr Neurol 2016 Mar 18;20(2):286-295. Epub 2015 Dec 18.

Manchester Centre for Genomic Medicine, St. Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK; Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2015.11.012DOI Listing
March 2016

Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.

Authors:
Yanick J Crow Diana S Chase Johanna Lowenstein Schmidt Marcin Szynkiewicz Gabriella M A Forte Hannah L Gornall Anthony Oojageer Beverley Anderson Amy Pizzino Guy Helman Mohamed S Abdel-Hamid Ghada M Abdel-Salam Sam Ackroyd Alec Aeby Guillermo Agosta Catherine Albin Stavit Allon-Shalev Montse Arellano Giada Ariaudo Vijay Aswani Riyana Babul-Hirji Eileen M Baildam Nadia Bahi-Buisson Kathryn M Bailey Christine Barnerias Magalie Barth Roberta Battini Michael W Beresford Geneviève Bernard Marika Bianchi Thierry Billette de Villemeur Edward M Blair Miriam Bloom Alberto B Burlina Maria Luisa Carpanelli Daniel R Carvalho Manuel Castro-Gago Anna Cavallini Cristina Cereda Kate E Chandler David A Chitayat Abigail E Collins Concepcion Sierra Corcoles Nuno J V Cordeiro Giovanni Crichiutti Lyvia Dabydeen Russell C Dale Stefano D'Arrigo Christian G E L De Goede Corinne De Laet Liesbeth M H De Waele Ines Denzler Isabelle Desguerre Koenraad Devriendt Maja Di Rocco Michael C Fahey Elisa Fazzi Colin D Ferrie António Figueiredo Blanca Gener Cyril Goizet Nirmala R Gowrinathan Kalpana Gowrishankar Donncha Hanrahan Bertrand Isidor Bülent Kara Nasaim Khan Mary D King Edwin P Kirk Ram Kumar Lieven Lagae Pierre Landrieu Heinz Lauffer Vincent Laugel Roberta La Piana Ming J Lim Jean-Pierre S-M Lin Tarja Linnankivi Mark T Mackay Daphna R Marom Charles Marques Lourenço Shane A McKee Isabella Moroni Jenny E V Morton Marie-Laure Moutard Kevin Murray Rima Nabbout Sheela Nampoothiri Noemi Nunez-Enamorado Patrick J Oades Ivana Olivieri John R Ostergaard Belén Pérez-Dueñas Julie S Prendiville Venkateswaran Ramesh Magnhild Rasmussen Luc Régal Federica Ricci Marlène Rio Diana Rodriguez Agathe Roubertie Elisabetta Salvatici Karin A Segers Gyanranjan P Sinha Doriette Soler Ronen Spiegel Tommy I Stödberg Rachel Straussberg Kathryn J Swoboda Mohnish Suri Uta Tacke Tiong Y Tan Johann te Water Naude Keng Wee Teik Maya Mary Thomas Marianne Till Davide Tonduti Enza Maria Valente Rudy Noel Van Coster Marjo S van der Knaap Grace Vassallo Raymon Vijzelaar Julie Vogt Geoffrey B Wallace Evangeline Wassmer Hannah J Webb William P Whitehouse Robyn N Whitney Maha S Zaki Sameer M Zuberi John H Livingston Flore Rozenberg Pierre Lebon Adeline Vanderver Simona Orcesi Gillian I Rice

Am J Med Genet A 2015 Feb 16;167A(2):296-312. Epub 2015 Jan 16.

INSERM UMR 1163, Laboratory of Neurogenetics and Neuroinflammation, Paris Descartes - Sorbonne Paris Cité University, Institut Imagine, Hôpital Necker, Paris, France; Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.

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http://dx.doi.org/10.1002/ajmg.a.36887DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382202PMC
February 2015

Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families.

J Community Genet 2010 Jun 20;1(2):73-81. Epub 2010 Aug 20.

Genetic Medicine and MAHSC, St. Mary's Hospital, Central Manchester University Hospitals, Manchester, M13 0JH, UK.

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http://dx.doi.org/10.1007/s12687-010-0012-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185987PMC
June 2010