Tabib Dabir

2.9k total citations
12 papers, 116 citations indexed

About

Tabib Dabir is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Tabib Dabir has authored 12 papers receiving a total of 116 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Tabib Dabir's work include Congenital Heart Disease Studies (2 papers), Cellular transport and secretion (2 papers) and Ocular Disorders and Treatments (2 papers). Tabib Dabir is often cited by papers focused on Congenital Heart Disease Studies (2 papers), Cellular transport and secretion (2 papers) and Ocular Disorders and Treatments (2 papers). Tabib Dabir collaborates with scholars based in United Kingdom, Netherlands and United States. Tabib Dabir's co-authors include Brendan Bunting, Briege M Lagan, Frank Casey, Patrick J. Morrison, Helen Dolk, Steven Hunter, Joanne Given, Brian Craig, C F J Russell and Maria Loane and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Tabib Dabir

12 papers receiving 115 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Tabib Dabir United Kingdom	6	45	41	27	21	17	12	116
Yongqing Sun China	8	58 1.3×	23 0.6×	13 0.5×	14 0.7×	7 0.4×	27	164
Elaine Barfield United States	7	44 1.0×	35 0.9×	29 1.1×	29 1.4×	8 0.5×	14	155
Sahar Elouej Tunisia	8	89 2.0×	85 2.1×	25 0.9×	32 1.5×	19 1.1×	19	173
Moritz Reiterer United Kingdom	4	67 1.5×	27 0.7×	6 0.2×	10 0.5×	7 0.4×	7	135
Danielle Moore United Kingdom	7	46 1.0×	21 0.5×	26 1.0×	108 5.1×	14 0.8×	11	191
Rita Valdéz Argentina	6	30 0.7×	46 1.1×	28 1.0×	23 1.1×	3 0.2×	10	171
Katie Sullivan Canada	8	56 1.2×	33 0.8×	6 0.2×	36 1.7×	10 0.6×	15	178
Nevbahar Tamçelik Türkiye	14	88 2.0×	26 0.6×	31 1.1×	8 0.4×	6 0.4×	31	499
Ashley Leinbach United States	4	31 0.7×	48 1.2×	13 0.5×	28 1.3×	4 0.2×	4	226
Guilherme Silva Julian Brazil	6	40 0.9×	12 0.3×	13 0.5×	13 0.6×	4 0.2×	32	157

Countries citing papers authored by Tabib Dabir

Since Specialization

Citations

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

Fields of papers citing papers by Tabib Dabir

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tabib Dabir

This figure shows the co-authorship network connecting the top 25 collaborators of Tabib Dabir. A scholar is included among the top collaborators of Tabib Dabir 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 Tabib Dabir. Tabib Dabir is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Pingault, Véronique, Berta Campos, Esther Nibbeling, et al.. (2024). Chromatin assembly factor subunit CHAF1A as a monogenic cause for oculo-auriculo-vertebral spectrum. European Journal of Human Genetics. 33(1). 131–136. 1 indexed citations

Pagnamenta, Alistair T., Jing Yu, Tracey Willis, et al.. (2023). A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and SRRM2 Haploinsufficiency. Human Mutation. 2023. 1–9. 2 indexed citations

Kuechler, Alma, Tabib Dabir, Stephanie Spranger, et al.. (2023). Novel Variants of SOX4 in Patients with Intellectual Disability. International Journal of Molecular Sciences. 24(4). 3519–3519. 2 indexed citations

Dolk, Helen, Frank Casey, Brian Craig, et al.. (2020). Risk factors for congenital heart disease: The Baby Hearts Study, a population-based case-control study. PLoS ONE. 15(2). e0227908–e0227908. 36 indexed citations

Johnston, Jennifer J., Kathleen A. Williamson, Julie C. Sapp, et al.. (2019). NAA10 polyadenylation signal variants cause syndromic microphthalmia. Journal of Medical Genetics. 56(7). 444–452. 22 indexed citations

Baralle, Diana, Tabib Dabir, Sarah Waller, et al.. (2018). Identification and functional analysis of a novel oculocerebrorenal syndrome of Lowe (OCRL) gene variant in two pedigrees with varying phenotypes including isolated congenital cataract.. PubMed. 24. 847–852. 4 indexed citations

Suri, Mohnish, Roman A. Laskowski, Kate Baker, et al.. (2017). Protein structure and phenotypic analysis of pathogenic and population missense variants inSTXBP1. Molecular Genetics & Genomic Medicine. 5(5). 495–507. 20 indexed citations

Dabir, Tabib, Fiona Stewart, & Nan Hill. (2009). Neural tube defects in 21st century: is Northern Ireland changing?. SHILAP Revista de lepidopterología. 6(S2). 1 indexed citations

Dabir, Tabib, Brian McCrossan, Louise Sweeney, Alex Magee, & Andrew J Sands. (2008). Down Syndrome, Achondroplasia and Tetralogy of Fallot. Neonatology. 94(1). 68–70. 6 indexed citations

10.

Dabir, Tabib, et al.. (2007). Cranio-osteoarthropathy in sibs. Clinical Dysmorphology. 16(3). 197–201. 6 indexed citations

11.

Dabir, Tabib. (2006). Oxford Desk Reference: Clinical Genetics. PubMed Central. 75(3). 235–235. 2 indexed citations

12.

Dabir, Tabib, et al.. (2006). The RET Mutation E768D Confers a Late-onset Familial Medullary Thyroid Carcinoma – Only Phenotype with Incomplete Penetrance: Implications for Screening and Management of Carrier Status. Familial Cancer. 5(2). 201–204. 14 indexed citations

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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