Sahar Mansour

10.2k citations

86 papers · 4.7k indexed · 1 hit paper · h-index 36

Impact in

Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
Oncology top 2%
- Lymphatic System and Diseases

Papers in

Oncology 34
- Lymphatic System and Diseases 30
Cell Biology 18
- Skin and Cellular Biology Research 11

Co-authors: Glen Brice Peter Mortimer Pia Østergaard Steve Jeffery M. Dominguez-Steglich I D Young Silvana Guioli Cheni Kwok
Journals: European Journal of Human Genetics (8 papers)European Journal of Medical Genetics (6 papers)Journal of Medical Genetics (6 papers)Human Genetics (5 papers)Clinical Genetics (5 papers)
Partner nations: United Kingdom United States France

In The Last Decade

Sahar Mansour

80 papers receiving 4.6k citations

Hit Papers

align trajectories log scale

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene 1994 · 1.2k citations

Peers

Countries citing papers authored by Sahar Mansour

Since Specialization

Citations

This map shows the geographic impact of Sahar Mansour's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sahar Mansour with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sahar Mansour more than expected).

Fields of papers citing papers by Sahar Mansour

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sahar Mansour. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sahar Mansour. The network helps show where Sahar Mansour may publish in the future.

Co-authors

The 25 scholars most cited alongside Sahar Mansour, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sahar Mansour Line = papers co-authored together Sahar Mansour links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Apoptosis induction and anti-inflammatory cytokines effects of sorafenib-loaded MXene-UiO-66@liposome nanocomposites in liver cancer under NIR irradiation Diamond and Related Materials ·Shehab Elbeltagi, Sahar Mansour, Hagar M El-Tohamy, M. Ismail, Khaled M Abdelbased, Mohammed M. Alanazi, Nada S Al-Theyab, Zienab E. Eldin	2025	0
2	Guidelines for the diagnosis and management of adult aplastic anaemia: A British Society for Haematology Guideline British Journal of Haematology ·Austin Kulasekararaj, Jamie Cavenagh, Inderjeet Dokal, Theodora Foukaneli, Shreyans Gandhi, Mamta Garg, Morag Griffin, Peter Hillmen, Robin Ireland, Sally Killick, Sahar Mansour, Ghulam Mufti, Victoria Potter, John A. Snowden, Simon Stanworth, Roslin Zuha, Judith Marsh	2024	35
3	Profound and selective lymphopaenia in primary lymphatic anomaly patients demonstrates the significance of lymphatic-lymphocyte interactions Frontiers in Immunology ·Julian Pearce, Linda Hadcocks, Sahar Mansour, Malou van Zanten, Steve Jeffery, Kristiana Gordon, Pia Østergaard, Peter Mortimer, Derek C. Macallan	2023	1
4	Consensus recommendations on lymphedema in Phelan-McDermid syndrome European Journal of Medical Genetics ·Robert J. Damstra, S. Vignes, Conny M.A. van Ravenswaaij‐Arts, Sahar Mansour	2023	3
5	Redefining WILD syndrome: a primary lymphatic dysplasia with congenital multisegmental lymphoedema, cutaneous lymphovascular malformation, CD4 lymphopaenia and warts Journal of Medical Genetics ·Sahar Mansour, Katherine Josephs, Pia Østergaard, Kristiana Gordon, Malou van Zanten, Julian Pearce, Steve Jeffery, Vaughan Keeley, Katie Riches, Alexander Kreuter, Ulrike Wieland, René Hägerling, Lakshmi Ratnam, Ege Sackey, Dionysios Grigoriadis, Bernard Ho, Frances Smith, Elisabeth Rauter, Peter Mortimer, Derek C. Macallan	2021	8
6	The St George's Classification Algorithm of Primary Lymphatic Anomalies Lymphatic Research and Biology ·Kristiana Gordon, Peter Mortimer, Malou van Zanten, Steve Jeffery, Pia Østergaard, Sahar Mansour	2021	14
7	Mosaicism in ASXL3-related syndrome: Description of five patients from three families European Journal of Medical Genetics ·Schaida Schirwani, Natalie Hauser, Anna Platt, Sumit Punj, Katrina Prescott, Natalie Canham, D.D.D. Study, Sahar Mansour, Meena Balasubramanian	2020	9
8	Lymphoscintigraphic Abnormalities Associated with Milroy Disease and Lymphedema-Distichiasis Syndrome Lymphatic Research and Biology ·Muberra Sarica, Kristiana Gordon, Malou van Zanten, Susan Heenan, Peter Mortimer, Andrew G. Irwin, Vijaya Ramachandra, Pia Østergaard, Sahar Mansour	2019	13
9	Human phenotypes caused by PIEZO1 mutations; one gene, two overlapping phenotypes? The Journal of Physiology ·Silvia Martin‐Almedina, Sahar Mansour, Pia Østergaard	2018	35
10	Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management Genetics in Medicine ·Natalie Chandler, Sunayna Best, Jane Hayward, Francesca Faravelli, Sahar Mansour, Emma Kivuva, Dagmar Tapon, Alison Male, Catherine DeVile, Lyn S. Chitty	2018	104
11	Abnormal Rab11‐Rab8‐vesicles cluster in enterocytes of patients with microvillus inclusion disease Traffic ·Georg F. Vogel, Andreas Janecke, Iris M. Krainer, Karin Gutleben, Barbara Witting, Sally G. Mitton, Sahar Mansour, Antje Ballauff, Joseph T. Roland, Amy C. Engevik, Ernest Cutz, Thomas Müller, James R. Goldenring, Lukas A. Huber, Michael W. Hess	2017	36
12	VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations JCI Insight ·René Hägerling, Dominik Drees, Aaron Scherzinger, Cathrin Dierkes, Silvia Martin‐Almedina, Stefan Butz, Kristiana Gordon, Michael Schäfers, Klaus Hinrichs, Pia Østergaard, Dietmar Vestweber, Tobias Goerge, Sahar Mansour, Xiaoyi Jiang, Peter Mortimer, Friedemann Kiefer	2017	29
13	The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome European Journal of Human Genetics ·Sarah Joyce, Kristiana Gordon, Glen Brice, Pia Østergaard, Rani Nagaraja, John Short, Sandra Moore, Peter Mortimer, Sahar Mansour	2015	54
14	A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family Clinical Genetics ·Glen Brice, Pia Østergaard, Steve Jeffery, Kristiana Gordon, P.S. Mortimer, Sahar Mansour	2013	58
15	A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Research ·Daniel A. King, Tomas Fitzgerald, Ray Miller, Natalie Canham, Jill Clayton‐Smith, Diana Johnson, Sahar Mansour, Fiona Stewart, Pradeep Vasudevan, Matthew E. Hurles, (unknown)	2013	54
16	Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci European Journal of Human Genetics ·Claire Turner, Deborah Mackay, Jonathan L A Callaway, Louise E Docherty, Rebecca Poole, H. Bullman, Margaret Lever, Bruce Castle, Emma Kivuva, Peter D. Turnpenny, Sarju Mehta, Sahar Mansour, Emma Wakeling, Verghese Mathew, J. Madden, Justin H. Davies, I. Karen Temple	2010	73
17	Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas Human Genetics ·Fiona Connell, Pia Østergaard, Charles Carver, Glen Brice, N. Williams, Sahar Mansour, P.S. Mortimer, Steve Jeffery	2009	1
18	A clinical and genetic study of the Say/Barber/Biesecker/Young‐Simpson type of Ohdo syndrome Clinical Genetics ·Richard O. Day, B Beckett, Dian Donnai, Alan Fryer, M. Heidenblad, Peter Howard, Bronwyn Kerr, Sahar Mansour, Una Maye, Shane McKee, Shehla Mohammed, Elizabeth Sweeney, May Tassabehji, BBA De Vries, Jill Clayton‐Smith	2008	17
19	Analysis of lymphoedema-distichiasis families forFOXC2 mutations reveals small insertions and deletions throughout the gene Human Genetics ·Rachel E. Bell, Glen Brice, Anne H. Child, V Murday, Sahar Mansour, C. Sandy, J R O Collin, Angela F. Brady, David F. Callen, K G Burnand, Peter Mortimer, Steve Jeffery	2001	96
20	The role of SOX9 in autosomal sex reversal and campomelic dysplasia Philosophical Transactions of the Royal Society B Biological Sciences ·Alan J. Schafer, M. Dominguez-Steglich, Silvana Guioli, Cheni Kwok, P A Weller, Milena Stevanović, J. Weissenbach, Sahar Mansour, I D Young, Peter N. Goodfellow, (unknown), (unknown)	1995	25

About Sahar Mansour

Sahar Mansour is a scholar working on Oncology, Cell Biology, Genetics, Pediatrics, Perinatology and Child Health and Surgery, having authored 86 papers that have together received 4.7k indexed citations. Recurring topics across this work include Lymphatic System and Diseases (30 papers), Vascular Malformations and Hemangiomas (17 papers), Genomic variations and chromosomal abnormalities (11 papers), Skin and Cellular Biology Research (11 papers), Prenatal Screening and Diagnostics (11 papers), Lymphatic Disorders and Treatments (8 papers), Genomics and Rare Diseases (7 papers) and Protein Tyrosine Phosphatases (5 papers). The work is most often cited by research in Genetics (1.9k citations), Oncology (1.2k citations), Reproductive Medicine (309 citations), Molecular Biology (2.2k citations) and Cell Biology (455 citations). Sahar Mansour has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Glen Brice, Peter Mortimer, Pia Østergaard, Steve Jeffery, M. Dominguez-Steglich, I D Young, Silvana Guioli, Cheni Kwok, Jamie W. Foster and J. David Brook. Their work appears in journals such as European Journal of Human Genetics, European Journal of Medical Genetics, Journal of Medical Genetics, Human Genetics and Clinical Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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