Morad Ansari

2.0k total citations
12 papers, 567 citations indexed

About

Morad Ansari is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Morad Ansari has authored 12 papers receiving a total of 567 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 2 papers in Genetics. Recurrent topics in Morad Ansari's work include Genomics and Chromatin Dynamics (4 papers), Genomics and Rare Diseases (3 papers) and Congenital Ear and Nasal Anomalies (2 papers). Morad Ansari is often cited by papers focused on Genomics and Chromatin Dynamics (4 papers), Genomics and Rare Diseases (3 papers) and Congenital Ear and Nasal Anomalies (2 papers). Morad Ansari collaborates with scholars based in United Kingdom, France and United States. Morad Ansari's co-authors include David Fitzpatrick, Martin S. Taylor, Alison Meynert, Veronica van Heyningen, Kathleen A. Williamson, Jacqueline K. Rainger, Wendy A. Bickmore, Hemant Bengani, Joe Rainger and Shelagh Boyle and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Morad Ansari

11 papers receiving 552 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Morad Ansari United Kingdom	10	365	303	54	48	48	12	567
Marjolaine Willems France	13	204 0.6×	156 0.5×	44 0.8×	68 1.4×	43 0.9×	39	531
Venkat Pulijaal United States	6	292 0.8×	157 0.5×	47 0.9×	51 1.1×	30 0.6×	9	424
Aleksander Jamsheer Poland	16	433 1.2×	397 1.3×	32 0.6×	57 1.2×	57 1.2×	77	731
Nadine Jalkh Lebanon	13	541 1.5×	238 0.8×	19 0.4×	49 1.0×	34 0.7×	38	751
Olivier Pichon France	13	416 1.1×	258 0.9×	16 0.3×	43 0.9×	22 0.5×	30	576
Carmelilia De Bernardo Italy	16	336 0.9×	261 0.9×	114 2.1×	22 0.5×	56 1.2×	32	612
Irina Balikova Belgium	12	179 0.5×	243 0.8×	53 1.0×	36 0.8×	29 0.6×	30	392
Maartje J. Vogel Netherlands	7	434 1.2×	158 0.5×	20 0.4×	29 0.6×	25 0.5×	9	578
Gabriele Gillessen-Kaesbach Germany	5	349 1.0×	265 0.9×	42 0.8×	32 0.7×	42 0.9×	5	506
Bisera Vukovic Canada	10	273 0.7×	123 0.4×	40 0.7×	35 0.7×	49 1.0×	11	463

Countries citing papers authored by Morad Ansari

Since Specialization

Citations

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

Fields of papers citing papers by Morad Ansari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Morad Ansari

This figure shows the co-authorship network connecting the top 25 collaborators of Morad Ansari. A scholar is included among the top collaborators of Morad Ansari 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 Morad Ansari. Morad Ansari 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

Abbott, Michael, Mandy Ryan, Rodolfo Hernández, et al.. (2024). Should Scotland provide genome-wide sequencing for the diagnosis of rare developmental disorders? A cost-effectiveness analysis. The European Journal of Health Economics. 26(3). 503–512.

Ansari, Morad, et al.. (2024). Curating genomic disease-gene relationships with Gene2Phenotype (G2P). Genome Medicine. 16(1). 127–127. 2 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

Ansari, Morad, Hemant Bengani, Graeme R. Grimes, et al.. (2018). BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange–like syndrome. Nature Genetics. 50(3). 329–332. 89 indexed citations

Moss, Joanna, Morad Ansari, Stephanie Barton, et al.. (2017). Genotype–phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with age. American Journal of Medical Genetics Part A. 173(6). 1566–1574. 18 indexed citations

Meynert, Alison, Morad Ansari, David Fitzpatrick, & Martin S. Taylor. (2014). Variant detection sensitivity and biases in whole genome and exome sequencing. BMC Bioinformatics. 15(1). 247–247. 138 indexed citations

Ansari, Morad, Jacqueline K. Rainger, Jennie Murray, et al.. (2014). A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX. European Journal of Medical Genetics. 57(10). 587–595. 16 indexed citations

Williamson, Kathleen A., Joe Rainger, James Floyd, et al.. (2014). Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects. The American Journal of Human Genetics. 94(2). 295–302. 77 indexed citations

Gordon, Christopher T., Catia Attanasio, Shipra Bhatia, et al.. (2014). Identification of Novel Craniofacial Regulatory Domains Located far Upstream ofSOX9and Disrupted in Pierre Robin Sequence. Human Mutation. 35(8). 1011–1020. 67 indexed citations

10.

Rainger, Joe, Smita Bhatia, Hemant Bengani, et al.. (2013). Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence. Human Molecular Genetics. 23(10). 2569–2579. 46 indexed citations

11.

Gerth‐Kahlert, Christina, Kathleen A. Williamson, Morad Ansari, et al.. (2013). Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center. Molecular Genetics & Genomic Medicine. 1(1). 15–31. 63 indexed citations

12.

Nolen, Leisha D., et al.. (2013). Regional chromatin decompaction in Cornelia de Lange syndrome associated with NIPBL disruption can be uncoupled from cohesin and CTCF. Human Molecular Genetics. 22(20). 4180–4193. 29 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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