Mette Gilling

699 total citations
7 papers, 124 citations indexed

About

Mette Gilling is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Mette Gilling has authored 7 papers receiving a total of 124 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Mette Gilling's work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Prenatal Screening and Diagnostics (2 papers). Mette Gilling is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Prenatal Screening and Diagnostics (2 papers). Mette Gilling collaborates with scholars based in Denmark, Germany and United Kingdom. Mette Gilling's co-authors include Karen Brøndum‐Nielsen, Niels Tommerup, Vera M. Kalscheuer, Zeynep Tümer, Esben Budtz–Jørgensen, Susanne E. Boonen, Jakob Christensen, Rikke S. Møller, Jørgen E. Nielsen and Kirsten Svenstrup and has published in prestigious journals such as The American Journal of Human Genetics, European Journal of Neurology and European Journal of Human Genetics.

In The Last Decade

Mette Gilling

7 papers receiving 111 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mette Gilling Denmark	6	66	64	41	22	19	7	124
Dana Marafi United States	8	70 1.1×	88 1.4×	22 0.5×	16 0.7×	10 0.5×	24	171
Nicoletta Zanotta Italy	8	53 0.8×	70 1.1×	59 1.4×	20 0.9×	11 0.6×	16	169
Rita Teek Estonia	9	124 1.9×	126 2.0×	34 0.8×	16 0.7×	5 0.3×	14	221
A Curtis United Kingdom	6	62 0.9×	137 2.1×	77 1.9×	30 1.4×	12 0.6×	7	201
Lisa Robertson United Kingdom	5	106 1.6×	95 1.5×	18 0.4×	20 0.9×	4 0.2×	8	154
A. T. Pagnamenta United Kingdom	3	81 1.2×	142 2.2×	33 0.8×	30 1.4×	2 0.1×	3	215
Renée Carroll Australia	6	82 1.2×	124 1.9×	48 1.2×	13 0.6×	11 0.6×	8	188
Tobias Brünger United States	5	48 0.7×	62 1.0×	28 0.7×	7 0.3×	14 0.7×	11	109
Donna Villasana United States	2	93 1.4×	137 2.1×	94 2.3×	19 0.9×	37 1.9×	2	237
Stephanie Karch Germany	8	50 0.8×	101 1.6×	23 0.6×	10 0.5×	3 0.2×	8	146

Countries citing papers authored by Mette Gilling

Since Specialization

Citations

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

Fields of papers citing papers by Mette Gilling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mette Gilling

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

All Works

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7 of 7 papers shown

1.

Gilling, Mette, Esben Budtz–Jørgensen, Susanne E. Boonen, et al.. (2017). The Danish HD Registry—a nationwide family registry of HD families in Denmark. Clinical Genetics. 92(3). 338–341. 7 indexed citations

2.

Gilling, Mette. (2015). Chromosomal Abnormalities and Putative Susceptibility Genes in Autism Spectrum Disorders. 1 indexed citations

3.

Gilling, Mette, Hanne B. Rasmussen, Kirstine Calløe, et al.. (2013). Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders. Frontiers in Genetics. 4. 54–54. 40 indexed citations

4.

Gilling, Mette, Allan Lind-Thomsen, Yuan Mang, et al.. (2011). Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation. European Journal of Medical Genetics. 54(4). e383–e388. 7 indexed citations

5.

Svenstrup, Kirsten, Rikke S. Møller, Jakob Christensen, et al.. (2011). NIPA1mutation in complex hereditary spastic paraplegia with epilepsy. European Journal of Neurology. 18(9). 1197–1199. 25 indexed citations

6.

Gilling, Mette, Marlene Briciet Lauritsen, Morten Møller, et al.. (2008). A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia. European Journal of Human Genetics. 16(3). 312–319. 14 indexed citations

7.

Gilling, Mette, Stefan Gesk, Reiner Siebert, et al.. (2006). Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation among Northern Europeans. The American Journal of Human Genetics. 78(5). 878–883. 30 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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