Concepedia

Author

Sheila Fisher

King's College LondonORCID

Also Known As

Emma Harvey, F. Duška, Hazel Drummond, Nilesh J Samani, S A Fisher, S Fisher, S. A. Fisher, S. Fisher, S.A. Fisher, Sheila A Fisher

168

Publications

64.2K

Citations

58

H-Index

100

Concepts

All Affiliations

King's College LondonBroad InstituteGuy's HospitalNewcastle UniversityUniversity College London
SF

About

Sheila Fisher is an author at King's College London specializing in medicine, pathology, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

29

31

15K

2

Engineering

2

2

1.5K

3

Health Sciences

2

2

582

4

Natural Sciences

2

2

2.5K

5

Management

1

1

58

Sheila Fisher

×

52

Publications

21.9K

Citations

41

H-Index

YearCitations

Genomic Classification of Cutaneous Melanoma

Rehan Akbani, Kadir C. Akdemir, Bülent Arman Aksoy,

Cell

2015

3.2K

Integrated Genomic Characterization of Papillary Thyroid Carcinoma

Nishant Agrawal, Rehan Akbani, Bülent Arman Aksoy,

Cell

2014

3K

Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype

Olivier Jaillon, Jean‐Marc Aury, Frédéric Brunet,

Nature

2004

2K

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

Andreas Gnirke, Alexandre Melnikov, Jared Maguire,

Nature Biotechnology

2009

1.5K

The genomic complexity of primary human prostate cancer

Michael F. Berger, Michael S. Lawrence, Francesca Demichelis,

Nature

2011

1.2K

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

Miles Parkes, Jeffrey C. Barrett, Natalie J. Prescott,

Nature Genetics

2007

1.2K

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

Jochen Hampe, Andrew Cuthbert, Peter J.P. Croucher,

The Lancet

2001

1.1K

Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

Andrea Rivera, Sheila Fisher, Lars G. Fritsche,

Human Molecular Genetics

2005

787

Exome Sequencing,<i>ANGPTL3</i>Mutations, and Familial Combined Hypolipidemia

Kiran Musunuru, James P. Pirruccello, Ron Do,

New England Journal of Medicine

2010

757

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

Andrew Cuthbert, Sheila Fisher, Muddassar M. Mirza,

Gastroenterology

2002

690

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