Neeti Ghali

5.6k total citations
34 papers, 515 citations indexed

About

Neeti Ghali is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Neeti Ghali has authored 34 papers receiving a total of 515 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Oncology. Recurrent topics in Neeti Ghali's work include Connective tissue disorders research (23 papers), Dermatological and Skeletal Disorders (9 papers) and Genomics and Rare Diseases (4 papers). Neeti Ghali is often cited by papers focused on Connective tissue disorders research (23 papers), Dermatological and Skeletal Disorders (9 papers) and Genomics and Rare Diseases (4 papers). Neeti Ghali collaborates with scholars based in United Kingdom, Canada and Netherlands. Neeti Ghali's co-authors include Angela F. Brady, Anthony Vandersteen, Glenda Sobey, Johannes Zschocke, Nigel Burrows, Ines Kapferer‐Seebacher, Tomoki Kosho, Cecilia Giunta, Fransiska Malfait and Nicol C. Voermans and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Neeti Ghali

31 papers receiving 509 citations

Peers

Countries citing papers authored by Neeti Ghali

Since Specialization

Citations

This map shows the geographic impact of Neeti Ghali'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 Neeti Ghali with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Neeti Ghali more than expected).

Fields of papers citing papers by Neeti Ghali

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Neeti Ghali. 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 Neeti Ghali. The network helps show where Neeti Ghali may publish in the future.

Co-authorship network of co-authors of Neeti Ghali

This figure shows the co-authorship network connecting the top 25 collaborators of Neeti Ghali. A scholar is included among the top collaborators of Neeti Ghali based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Neeti Ghali. Neeti Ghali is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome 2025 ·European Journal of Human Genetics ·(unknown), Shadi Albaba, Glenda Sobey, Jessica Bowen, Deirdre E. Donnelly, Marina Colombi, Marco Ritelli, (unknown), Neeti Ghali, Fleur S. van Dijk, Emma Hobson, (unknown), Esther Kinning, Abhijit Dixit, (unknown), Duncan Baker, Diana Johnson	0
2	Clinical diagnosis of the monogenic Ehlers-Danlos syndromes 2024 ·Medizinische Genetik ·Fleur S. van Dijk, (unknown), Serwet Demirdas, Neeti Ghali, Johannes Zschocke	0
3	The Natural History of Dermatosparaxis Ehlers Danlos Syndrome: An Adult Case Series 2024 ·American Journal of Medical Genetics Part A ·(unknown), Peter H. Byers, (unknown), Neeti Ghali, Juliette Harris, Ingrid Haußer, (unknown), Glenda Sobey, Fleur S. van Dijk	1
4	Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhood 2024 ·European Journal of Human Genetics ·Nafisa Wilkinson, Elena Cervi, Bart Wagner, Déborah Morris-Rosendahl, Duncan Baker, (unknown), (unknown), Toby Andrew, Neeti Ghali, Fleur S. van Dijk	1
5	A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and SRRM2 Haploinsufficiency 2023 ·Human Mutation ·Alistair T. Pagnamenta, Jing Yu, Tracey Willis, (unknown), Eleanor G. Seaby, Susan Walker, (unknown), (unknown), Ana Lisa Taylor Tavares, Francesca Forzano, Helen Cox, Tabib Dabir, Angela F. Brady, Neeti Ghali, Santosh S. Atanur, Sarah Ennis, Diana Baralle, Jenny C. Taylor	2
6	Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome 2023 ·Journal of Medical Genetics ·Anthony M. Vandersteen, Ruwan Weerakkody, David Parry, (unknown), (unknown), Jana Vandrovcová, Rebecca Darlay, Javier Santoyo‐López, Alison Meynert, (unknown), Hanadi Kazkaz, Rodney Grahame, (unknown), (unknown), Neeti Ghali, Angela F. Brady, F M Pope, Fleur S. van Dijk, Heather J. Cordell, Timothy J. Aitman	7
7	Ehlers-Danlos syndromes: importance of defining the type 2023 ·Practical Neurology ·Fleur S. van Dijk, Neeti Ghali, Arvind Chandratheva	3
8	Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants 2023 ·Frontiers in Genetics ·(unknown), Neeti Ghali, (unknown)	8
9	An exemplary model of genetic counselling for highly specialised services 2023 ·Journal of Community Genetics ·Juliette Harris, (unknown), Duncan Baker, (unknown), Jessica Bowen, (unknown), (unknown), Claire Green, (unknown), (unknown), (unknown), (unknown), Clare L. Stacey, Jan M. Cobben, Neeti Ghali, Diana Johnson, Glenda Sobey, Fleur S. van Dijk	2
10	Case report and discussion: Pre-implantation genetic diagnosis with surrogacy in vascular Ehlers–Danlos syndrome 2023 ·Frontiers in Genetics ·(unknown), Neeti Ghali, (unknown)	1
11	Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UK 2022 ·European Journal of Medical Genetics ·(unknown), Fleur S. van Dijk, Matthew Cauldwell, Rachel Harrison, Alison Kraus, Paul Brennan, Neeti Ghali, Nayana Lahiri, Diana Johnson, Glenda Sobey	4
12	Classical-like Ehlers–Danlos syndrome: a clinical description of 20 newly identified individuals with evidence of tissue fragility 2020 ·Genetics in Medicine ·(unknown), Neeti Ghali, (unknown), (unknown), Duncan Baker, (unknown), Jessica Bowen, Angela F. Brady, (unknown), (unknown), (unknown), Vivienne McConnell, (unknown), Hanadi Kazkaz, Diana Johnson, F. Michael Pope, Anthony Vandersteen, Glenda Sobey, Fleur S. van Dijk	17
13	Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers‐Danlos syndrome 2020 ·American Journal of Medical Genetics Part A ·(unknown), Neeti Ghali, (unknown), Duncan Baker, (unknown), Angela F. Brady, Maria Luisa Giovannucci Uzielli, Cecilia Giunta, Diana Johnson, Tomoki Kosho, Katherine Neas, F M Pope, Frank Rutsch, (unknown), Glenda Sobey, Anthony Vandersteen, Fleur S. van Dijk	14
14	Prospective clinical investigations of children with periodontal Ehlers–Danlos syndrome identify generalized lack of attached gingiva as a pathognomonic feature 2020 ·Genetics in Medicine ·Ines Kapferer‐Seebacher, (unknown), (unknown), Diana Johnson, Neeti Ghali, Angela F. Brady, Glenda Sobey, Johannes Zschocke, Fleur S. van Dijk	16
15	Electron microscopy in the diagnosis of Ehlers–Danlos syndromes: correlation with clinical and genetic investigations 2019 ·British Journal of Dermatology ·(unknown), Neeti Ghali, Duncan Baker, Angela F. Brady, F. Michael Pope, Anthony Vandersteen, Bart Wagner, David Ferguson, Fleur S. van Dijk	20
16	Absence of Collagen Flowers on Electron Microscopy and Identification of (Likely) Pathogenic COL5A1 Variants in Two Patients 2019 ·Genes ·(unknown), Angela F. Brady, Marina Colombi, David Ferguson, Rebecca C. Pollitt, F. Michael Pope, Marco Ritelli, Sofie Symoens, Neeti Ghali, Fleur S. van Dijk	11
17	Ehlers-Danlos syndromes 2019 ·BMJ ·Neeti Ghali, Glenda Sobey, Nigel Burrows	35
18	Recessive NEK9 mutation causes a lethal skeletal dysplasia with evidence of cell cycle and ciliary defects 2016 ·Human Molecular Genetics ·Jillian P. Casey, Kieran Brennan, (unknown), Paul McGettigan, (unknown), (unknown), Sean Ennis, Huw Dorkins, Neeti Ghali, Oliver E. Blacque, Margaret M. Mc Gee, Helen Murphy, Sally Ann Lynch	33
19	Targeted next-generation sequencing makes new molecular diagnoses and expands genotype–phenotype relationship in Ehlers–Danlos syndrome 2016 ·Genetics in Medicine ·Ruwan Weerakkody, Jana Vandrovcová, (unknown), Michael Mueller, Piyush Gampawar, (unknown), Penny J. Norsworthy, Jennifer Biggs, (unknown), David Ross, (unknown), David Ferguson, Nicholas Cheshire, Hanadi Kazkaz, Rodney Grahame, Neeti Ghali, Anthony Vandersteen, F M Pope, Timothy J. Aitman	45
20	SAMS, a Syndrome of Short Stature, Auditory-Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Is a Unique Neurocristopathy Caused by Mutations in Goosecoid 2013 ·The American Journal of Human Genetics ·David Parry, Clare V. Logan, Alexander P.A. Stegmann, Zakia A. Abdelhamed, Alistair Calder, (unknown), David T. Bonthron, Virginia Clowes, Eamonn Sheridan, Neeti Ghali, Albert E. Chudley, Angus Dobbie, Constance T. R. M. Stumpel, Colin A. Johnson	27

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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