M. Durner

686 total citations
9 papers, 555 citations indexed

About

M. Durner is a scholar working on Genetics, Rheumatology and Psychiatry and Mental health. According to data from OpenAlex, M. Durner has authored 9 papers receiving a total of 555 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Rheumatology and 4 papers in Psychiatry and Mental health. Recurrent topics in M. Durner's work include Genetics and Neurodevelopmental Disorders (6 papers), Epilepsy research and treatment (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). M. Durner is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Epilepsy research and treatment (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). M. Durner collaborates with scholars based in United States, Germany and Canada. M. Durner's co-authors include Diéter Janz, David A. Greenberg, G. Beck‐Mannagetta, Antonio V. Delgado‐Escueta, T. Sander, Keith Johnson, A. Scaramelli, M. Anne Spence, R S Sparkes and Karen Weissbecker and has published in prestigious journals such as Neurology, Epilepsia and American Journal of Medical Genetics.

In The Last Decade

M. Durner

9 papers receiving 540 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Durner United States	8	352	348	141	139	114	9	555
G. Beck‐Mannagetta Germany	11	478 1.4×	310 0.9×	183 1.3×	211 1.5×	256 2.2×	14	717
Sergio Córdova Mexico	10	284 0.8×	176 0.5×	89 0.6×	142 1.0×	120 1.1×	12	441
Gregorio Pineda Spain	5	252 0.7×	156 0.4×	118 0.8×	131 0.9×	97 0.9×	6	408
Sibylle Wallace United States	6	219 0.6×	203 0.6×	99 0.7×	89 0.6×	77 0.7×	8	334
R. Gaggero Italy	16	396 1.1×	227 0.7×	162 1.1×	153 1.1×	199 1.7×	33	715
Rebekka Kretz Germany	12	403 1.1×	111 0.3×	123 0.9×	169 1.2×	261 2.3×	16	627
Suha Mercho Canada	5	280 0.8×	173 0.5×	182 1.3×	164 1.2×	96 0.8×	6	459
Lata Vadlamudi Australia	14	396 1.1×	323 0.9×	215 1.5×	148 1.1×	156 1.4×	30	721
Noriyuki Akasaka Japan	14	214 0.6×	245 0.7×	175 1.2×	122 0.9×	122 1.1×	27	566
Masako Sakauchi Japan	10	305 0.9×	123 0.4×	165 1.2×	141 1.0×	128 1.1×	18	503

Countries citing papers authored by M. Durner

Since Specialization

Citations

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

Fields of papers citing papers by M. Durner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Durner

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

All Works

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9 of 9 papers shown

1.

Slager, Susan L., Suh‐Hang Hank Juo, M. Durner, & Susan E. Hodge. (2001). Markov Chain Monte Carlo Linkage Analysis: Effect of Bin Width on the Probability of Linkage. Genetic Epidemiology. 21(S1). S700–5. 2 indexed citations

2.

Greenberg, David A., M. Durner, Stanley R. Resor, David Rosenbaum, & Shlomo Shinnar. (1995). The genetics of idiopathic generalized epilepsies of adolescent onset. Neurology. 45(5). 942–946. 48 indexed citations

3.

Durner, M., Diéter Janz, J. Zingsem, & David A. Greenberg. (1992). Possible Association of Juvenile Myoclonic Epilepsy with HLA‐DRw6. Epilepsia. 33(5). 814–816. 27 indexed citations

4.

Durner, M., David A. Greenberg, & Susan E. Hodge. (1992). Inter- and intrafamilial heterogeneity: effective sampling strategies and comparison of analysis methods.. PubMed. 51(4). 859–70. 51 indexed citations

5.

Durner, M., et al.. (1992). Evidence for multiple gene loci in the expression of the common generalized epilepsies.. PubMed. 42(4 Suppl 5). 56–62. 61 indexed citations

6.

Durner, M., David A. Greenberg, & Antonio V. Delgado‐Escueta. (1992). Is there a genetic relationship between epilepsy and birth defects?. PubMed. 42(4 Suppl 5). 63–7. 16 indexed citations

7.

Weissbecker, Karen, M. Durner, Diéter Janz, et al.. (1991). Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6. American Journal of Medical Genetics. 38(1). 32–36. 129 indexed citations

8.

Durner, M., T. Sander, David A. Greenberg, et al.. (1991). Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients. Neurology. 41(10). 1651–1651. 155 indexed citations

9.

Janz, Diéter, et al.. (1989). Family Studies on the Genetics of Juvenile Myoclonic Epilepsy (Epilepsy with Impulsive Petit Mal). PubMed. 56 Suppl Pt 1. 43–52. 66 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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