Amna Khamis

741 total citations
11 papers, 214 citations indexed

About

Amna Khamis is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Amna Khamis has authored 11 papers receiving a total of 214 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Surgery. Recurrent topics in Amna Khamis's work include Epigenetics and DNA Methylation (5 papers), Pancreatic function and diabetes (4 papers) and Genetic Associations and Epidemiology (2 papers). Amna Khamis is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), Pancreatic function and diabetes (4 papers) and Genetic Associations and Epidemiology (2 papers). Amna Khamis collaborates with scholars based in United Kingdom, France and United States. Amna Khamis's co-authors include Philippe Froguel, Amélie Bonnefond, Mickaël Canouil, Mathilde Boissel, Arie Nouwen, Anna Ulrich, Inga Prokopenko, Marika Kaakinen, Zhanna Balkhiyarova and Stéphane Lobbens and has published in prestigious journals such as Diabetes Care, The FASEB Journal and International Journal of Obesity.

In The Last Decade

Amna Khamis

11 papers receiving 210 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amna Khamis United Kingdom	8	77	72	52	34	29	11	214
Jixing Liang China	9	77 1.0×	31 0.4×	31 0.6×	69 2.0×	43 1.5×	17	314
Debbie Zittema Netherlands	10	143 1.9×	171 2.4×	20 0.4×	19 0.6×	20 0.7×	11	331
Akiko Hosokawa Japan	8	67 0.9×	25 0.3×	64 1.2×	75 2.2×	23 0.8×	9	282
Ana Carolina Proença da Fonseca Brazil	11	83 1.1×	109 1.5×	58 1.1×	87 2.6×	26 0.9×	31	292
Mayu Watanabe Japan	9	66 0.9×	17 0.2×	38 0.7×	39 1.1×	33 1.1×	32	256
Panagiota Pagoni United Kingdom	6	44 0.6×	64 0.9×	20 0.4×	40 1.2×	8 0.3×	8	196
Ian Seetho United Kingdom	11	42 0.5×	40 0.6×	45 0.9×	121 3.6×	43 1.5×	17	337
Teresia Wangensteen Norway	10	97 1.3×	120 1.7×	23 0.4×	52 1.5×	40 1.4×	16	295
Ewa Otto-Buczkowska Poland	8	26 0.3×	43 0.6×	50 1.0×	46 1.4×	81 2.8×	56	213

Countries citing papers authored by Amna Khamis

Since Specialization

Citations

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

Fields of papers citing papers by Amna Khamis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amna Khamis

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

Morán, Ignasi, Amélie Bonnefond, Amna Khamis, et al.. (2024). Multiple genetic variants at the SLC30A8 locus affect local super‐enhancer activity and influence pancreatic β‐cell survival and function. The FASEB Journal. 38(8). e23610–e23610. 2 indexed citations

Balkhiyarova, Zhanna, Arie Nouwen, Anna Ulrich, et al.. (2023). Bidirectional Mendelian Randomization and Multiphenotype GWAS Show Causality and Shared Pathophysiology Between Depression and Type 2 Diabetes. Diabetes Care. 46(9). 1707–1714. 56 indexed citations

Khamis, Amna, Beverley Balkau, Amélie Bonnefond, et al.. (2022). Epigenetic changes associated with hyperglycaemia exposure in the longitudinal D.E.S.I.R. cohort. Diabetes & Metabolism. 48(4). 101347–101347. 2 indexed citations

Canouil, Mickaël, Amna Khamis, Elina Keikkala, et al.. (2021). Epigenome-Wide Association Study Reveals Methylation Loci Associated With Offspring Gestational Diabetes Mellitus Exposure and Maternal Methylome. Diabetes Care. 44(9). 1992–1999. 21 indexed citations

Hu, Ming, Inês Cebola, Gaëlle Carrat, et al.. (2021). Chromatin 3D interaction analysis of the STARD10 locus unveils FCHSD2 as a regulator of insulin secretion. Cell Reports. 34(5). 108703–108703. 7 indexed citations

Khamis, Amna, Raphaël Boutry, Mickaël Canouil, et al.. (2020). Histone deacetylase 9 promoter hypomethylation associated with adipocyte dysfunction is a statin-related metabolic effect. Clinical Epigenetics. 12(1). 68–68. 12 indexed citations

Huyvaert, Marlène, Mickaël Canouil, Cécile Lecœur, et al.. (2019). The expression of genes in top obesity-associated loci is enriched in insula and substantia nigra brain regions involved in addiction and reward. International Journal of Obesity. 44(2). 539–543. 40 indexed citations

Khamis, Amna, Mickaël Canouil, Afshan Siddiq, et al.. (2019). Laser capture microdissection of human pancreatic islets reveals novel eQTLs associated with type 2 diabetes. Molecular Metabolism. 24. 98–107. 22 indexed citations

Khamis, Amna, Jutta Palmen, Nicholas Lench, et al.. (2014). Functional analysis of four LDLR 5′UTR and promoter variants in patients with familial hypercholesterolaemia. European Journal of Human Genetics. 23(6). 790–795. 22 indexed citations

10.

Khamis, Amna, Michael N. Weedon, Mark Walker, et al.. (2011). Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetes. Diabetic Medicine. 28(6). 681–684. 10 indexed citations

11.

Traboulsi, Elias I., et al.. (2000). Evidence of genetic heterogeneity in autosomal recessive congenital fibrosis of the extraocular muscles. American Journal of Ophthalmology. 129(5). 658–662. 20 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.

Explore authors with similar magnitude of impact