Saba Sharif - Concepedia

Author

Saba Sharif

Also Known As

Charles Shaw-Smith, Karina Rønlund, Natalie Canham, Nora Shannon, Roldan Singzon, Ruth McGowan, Saba Habib Sharif, Saba Sharif

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

St. Mary's Hospital University of Manchester St Mary's Hospital Manchester Royal Infirmary Inserm

About

Saba Sharif is an author at St. Mary's Hospital specializing in medicine, pathogenesis, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	264
2	Pathology	1	1	15
3	Developmental Biology	1	1	249
4	Genetics	1	1	249
5	Neuropathology	1	1	249

Saba Sharif

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Second Primary Tumors in Neurofibromatosis 1 Patients Treated for Optic Glioma: Substantial Risks After Radiotherapy Saba Sharif, Rosalie E. Ferner, Jillian M. Birch, Journal of Clinical Oncology	2006	368
Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas Miriam J. Smith, James O’Sullivan, Sanjeev S. Bhaskar, Nature Genetics Rare DiseasesDevelopmental BiologyMultiple Spinal MeningiomasMendelian DisorderGenetic Disorder	2013	249
Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures Daniele Cassatella, Sasha Howard, James S. Acierno, European Journal of Endocrinology	2018	128
Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial Michael Mullen, Xu Yu Jin, Anne H. Child, The Lancet	2019	128
Pathogenic Mitochondrial t <scp>RNA</scp> Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease Emma L. Blakely, John W. Yarham, Charlotte L. Alston, Human Mutation	2013	77
Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype Meena Balasubramanian, Alexander J.M. Dingemans, Shadi Albaba, European Journal of Human Genetics	2021	32
Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis Emma Mm Burkitt Wright, Emma K Sach, Saba Sharif, Journal of Medical Genetics	2013	31
Craniosynostosis with Ectopia Lentis and a Homozygous 20-base Deletion in ADAMTSL4 Aman Chandra, José Antonio Aragon-Martin, Saba Sharif, Ophthalmic Genetics	2012	24
Characterization of Missense Mutations and Large Deletions in the <i>ALPL</i> Gene by Sequencing and Quantitative Multiplex PCR of Short Fragments Marc Spentchian, Isabelle Brun‐Heath, A. Taillandier, Genetic Testing	2006	24
Hypophosphatasia: molecular testing of 19 prenatal cases and discussion about genetic counseling Brigitte Simon‐Bouy, A. Taillandier, Delphine Fauvert, Prenatal Diagnosis	2008	24

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