Wound healing potentials of Thevetia peruviana: Antioxidants and inflammatory markers criteria

por Rahman, Nazneen, Rahman, Haseebur, Haris, Mir, Mahmood, Riaz
Publicado 2017

Insights into BRCA Cancer Predisposition from Integrated Germline and Somatic Analyses in 7632 Cancers

por Yost, Shawn, Ruark, Elise, Alexandrov, Ludmil B, Rahman, Nazneen
Publicado 2019

Development of cancer genetic services in the UK: A national consultation

por Slade, Ingrid, Riddell, Daniel, Turnbull, Clare, Hanson, Helen, Rahman, Nazneen
Publicado 2015

A cost analysis of a cancer genetic service model in the UK

por Slade, Ingrid, Hanson, Helen, George, Angela, Kohut, Kelly, Strydom, Ann, Wordsworth, Sarah, Rahman, Nazneen
Publicado 2016

A Cost-Effectiveness Evaluation of Germline BRCA1 and BRCA2 Testing in UK Women with Ovarian Cancer

por Eccleston, Anthony, Bentley, Anthony, Dyer, Matthew, Strydom, Ann, Vereecken, Wim, George, Angela, Rahman, Nazneen
Publicado 2017

The ICR639 CPG NGS validation series: A resource to assess analytical sensitivity of cancer predisposition gene testing

por Mahamdallie, Shazia, Ruark, Elise, Holt, Esty, Poyastro-Pearson, Emma, Renwick, Anthony, Strydom, Ann, Seal, Sheila, Rahman, Nazneen
Publicado 2018

Oncologist-led BRCA ‘mainstreaming’ in the ovarian cancer clinic: A study of 255 patients and its impact on their management

por Rumford, Megan, Lythgoe, Mark, McNeish, Iain, Gabra, Hani, Tookman, Laura, Rahman, Nazneen, George, Angela, Krell, Jonathan
Publicado 2020

OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis

por Ruark, Elise, Münz, Márton, Clarke, Matthew, Renwick, Anthony, Ramsay, Emma, Elliott, Anna, Seal, Sheila, Lunter, Gerton, Rahman, Nazneen
Publicado 2016

ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling performance using the ICR142 NGS validation series

por Ruark, Elise, Holt, Esty, Renwick, Anthony, Münz, Márton, Wakeling, Matthew, Ellard, Sian, Mahamdallie, Shazia, Yost, Shawn, Rahman, Nazneen
Publicado 2018

CoverView: a sequence quality evaluation tool for next generation sequencing data

por Münz, Márton, Mahamdallie, Shazia, Yost, Shawn, Rimmer, Andrew, Poyastro-Pearson, Emma, Strydom, Ann, Seal, Sheila, Ruark, Elise, Rahman, Nazneen
Publicado 2018

The Quality Sequencing Minimum (QSM): providing comprehensive, consistent, transparent next generation sequencing  data quality assurance

por Mahamdallie, Shazia, Ruark, Elise, Yost, Shawn, Münz, Márton, Renwick, Anthony, Poyastro-Pearson, Emma, Strydom, Ann, Seal, Sheila, Rahman, Nazneen
Publicado 2018

Genomic variant sharing: a position statement

por Wright, Caroline F., Ware, James S., Lucassen, Anneke M., Hall, Alison, Middleton, Anna, Rahman, Nazneen, Ellard, Sian, Firth, Helen V.
Publicado 2019

The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis

por Ruark, Elise, Renwick, Anthony, Clarke, Matthew, Snape, Katie, Ramsay, Emma, Elliott, Anna, Hanks, Sandra, Strydom, Ann, Seal, Sheila, Rahman, Nazneen
Publicado 2018

CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting

por Münz, Márton, Ruark, Elise, Renwick, Anthony, Ramsay, Emma, Clarke, Matthew, Mahamdallie, Shazia, Cloke, Victoria, Seal, Sheila, Strydom, Ann, Lunter, Gerton, Rahman, Nazneen
Publicado 2015

Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN

por Fowler, Anna, Mahamdallie, Shazia, Ruark, Elise, Seal, Sheila, Ramsay, Emma, Clarke, Matthew, Uddin, Imran, Wylie, Harriet, Strydom, Ann, Lunter, Gerton, Rahman, Nazneen
Publicado 2016

The ICR96 exon CNV validation series: a resource for orthogonal assessment of exon CNV calling in NGS data

por Mahamdallie, Shazia, Ruark, Elise, Yost, Shawn, Ramsay, Emma, Uddin, Imran, Wylie, Harriett, Elliott, Anna, Strydom, Ann, Renwick, Anthony, Seal, Sheila, Rahman, Nazneen
Publicado 2017

The ICR1000 UK exome series: a resource of gene variation in an outbred population

por Ruark, Elise, Münz, Márton, Renwick, Anthony, Clarke, Matthew, Ramsay, Emma, Hanks, Sandra, Mahamdallie, Shazia, Elliott, Anna, Seal, Sheila, Strydom, Ann, Gerton, Lunter, Rahman, Nazneen
Publicado 2015

Recognition of and Response to Neonatal Intrapartum-related Complications in Home-birth Settings in Bangladesh

por VanderEnde, Kristin E., Moran, Allisyn C., Leasure, Karen, Day, Louise T., Afsana, Kaosar, Kalim, Nahid, Munira, Shirajum, Rahman, Nazneen, Islam, Munia, Khan, Jasmin, Sibley, Lynn M.
Publicado 2014

Mosaic-variegated aneuploidy syndrome mutation or haploinsufficiency in Cep57 impairs tumor suppression

por Aziz, Khaled, Sieben, Cynthia J., Jeganathan, Karthik B., Hamada, Masakazu, Davies, Brian A., Velasco, Raul O. Fierro, Rahman, Nazneen, Katzmann, David J., van Deursen, Jan M.
Publicado 2018

Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients

por George, Angela, Riddell, Daniel, Seal, Sheila, Talukdar, Sabrina, Mahamdallie, Shazia, Ruark, Elise, Cloke, Victoria, Slade, Ingrid, Kemp, Zoe, Gore, Martin, Strydom, Ann, Banerjee, Susana, Hanson, Helen, Rahman, Nazneen
Publicado 2016