Concepedia

Author

Shazia Mahamdallie

Institute of Cancer Research

Also Known As

Mahamdallie, Shazia, Mahamdallie, Shazia Sophie, S Mahamdallie, S S Mahamdallie, S.S. Mahamdallie, Shazia Mahamdallie, Shazia S Mahamdallie, Shazia S. Mahamdallie

46

Publications

2.1K

Citations

20

H-Index

57

Concepts

All Affiliations

Institute of Cancer ResearchRoyal Marsden NHS Foundation TrustNatural History MuseumUniversity College LondonGreat Ormond Street Hospital
SM

About

Shazia Mahamdallie is an author at Institute of Cancer Research specializing in medicine, evolutionary biology, and biology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

9

9

500

2

Natural Sciences

6

6

302

3

Biology

6

6

305

4

Public Health

3

3

148

5

Engineering

1

1

11

Shazia Mahamdallie

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24

Publications

2.1K

Citations

20

H-Index

YearCitations

Resolving the full spectrum of human genome variation using Linked-Reads

Patrick Marks, Sarah Garcia, Álvaro Martínez Barrio,

Genome Research

2019

290

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

Angela George, Daniel Riddell, Sheila Seal,

Scientific Reports

2016

215

Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability

Katrina Tatton‐Brown, Chey Loveday, Shawn Yost,

The American Journal of Human Genetics

2017

208

Protistan community analysis: key findings of a large-scale molecular sampling

Manfred Jensen, Dominik Heider, Steffen Jost,

The ISME Journal

2016

167

Identification of new Wilms tumour predisposition genes: an exome sequencing study

Shazia Mahamdallie, Shawn Yost, Emma Poyastro-Pearson,

The Lancet Child & Adolescent Health

2019

143

Evaluation of Cancer-Based Criteria for Use in Mainstream<i>BRCA1</i>and<i>BRCA2</i>Genetic Testing in Patients With Breast Cancer

Zoe Kemp, Alice Turnbull, Shawn Yost,

JAMA Network Open

2019

114

The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants

Katrina Tatton‐Brown, Anna Zachariou, Chey Loveday,

Wellcome Open Research

2018

106

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

Anna Fowler, Shazia Mahamdallie, Elise Ruark,

Wellcome Open Research

2016

105

Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour

Sandra Hanks, Elizabeth R Perdeaux, Sheila Seal,

Nature Communications

2014

98

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

Márton Münz, Elise Ruark, Anthony Renwick,

Genome Medicine

2015

91

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