M Wehnert

1.4k total citations · 1 hit paper
19 papers, 1.0k citations indexed

About

M Wehnert is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, M Wehnert has authored 19 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Hematology and 3 papers in Genetics. Recurrent topics in M Wehnert's work include Hemophilia Treatment and Research (6 papers), RNA and protein synthesis mechanisms (3 papers) and RNA Research and Splicing (3 papers). M Wehnert is often cited by papers focused on Hemophilia Treatment and Research (6 papers), RNA and protein synthesis mechanisms (3 papers) and RNA Research and Splicing (3 papers). M Wehnert collaborates with scholars based in Germany, United States and Belgium. M Wehnert's co-authors include Orly Reiner, Ying H. Shen, Fabrizia Faustinella, William B. Dobyns, David H. Ledbetter, Olga Zhuchenko, K. Wulff, Jennifer M. Bailey, Zhong Sheng Sun and W. Schröder and has published in prestigious journals such as Nature, Blood and Genome Research.

In The Last Decade

M Wehnert

19 papers receiving 1.0k citations

Hit Papers

Isolation of a Miller–Dicker lissencephaly gene containin... 1993 2026 2004 2015 1993 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats
    1993 824 citations Orly Reiner, Ying H. Shen et al. Nature profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M Wehnert Germany 9 674 319 284 199 195 19 1.0k
A. Dautigny France 16 626 0.9× 105 0.3× 136 0.5× 203 1.0× 209 1.1× 31 1.0k
Shinji Hirotsune Japan 15 1.1k 1.6× 282 0.9× 440 1.5× 95 0.5× 120 0.6× 25 1.4k
Sachiko Aono Japan 17 556 0.8× 489 1.5× 138 0.5× 135 0.7× 286 1.5× 36 996
Yong Ha Youn United States 11 700 1.0× 316 1.0× 263 0.9× 253 1.3× 173 0.9× 13 967
Hervé Pointu France 11 855 1.3× 368 1.2× 202 0.7× 51 0.3× 138 0.7× 12 1.2k
Grace M. Hobson United States 23 851 1.3× 85 0.3× 297 1.0× 140 0.7× 246 1.3× 42 1.2k
Stephanie Bielas United States 19 723 1.1× 274 0.9× 313 1.1× 145 0.7× 181 0.9× 44 1.1k
Marı́a José Barallobre Spain 15 575 0.9× 206 0.6× 257 0.9× 289 1.5× 420 2.2× 18 1.2k
Ma Salomé Sirerol-Piquer Spain 16 832 1.2× 260 0.8× 688 2.4× 121 0.6× 172 0.9× 26 1.2k
Zhicheng Mo United States 9 479 0.7× 177 0.6× 60 0.2× 159 0.8× 147 0.8× 12 856

Countries citing papers authored by M Wehnert

Since Specialization
Citations

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

Fields of papers citing papers by M Wehnert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Wehnert

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

All Works

19 of 19 papers shown
1.
Bonne, Gisèle, Rabah Ben Yaou, L. Demay, et al.. (2002). Clinical analysis of 32 patients carrying R453W LMNA mutation. UCL Discovery (University College London). 2 indexed citations
2.
Talvik, Inga, Hiljar Sibul, Arjen Kolk, et al.. (2002). Early onset of cardiomyopathy in two brothers with X-linked Emery–Dreifuss muscular dystrophy. Neuromuscular Disorders. 12(9). 878–881. 10 indexed citations
3.
Zhuchenko, Olga, et al.. (1999). Identification, mapping, and genomic structure of a novel X-chromosomal human gene (SMPX) encoding a small muscular protein. Human Genetics. 105(5). 506–512. 12 indexed citations
4.
Kuhlenbäeumer, Gregor, Jan Meuleman, Anja Schirmacher, et al.. (1998). Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c‐myb ET‐locus in two families with hereditary neuralgic amyotrophy (HNA). Annals of Human Genetics. 62(5). 397–400. 8 indexed citations
5.
Wulff, K., et al.. (1997). Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysis.. PubMed. 13(2). 77–86. 5 indexed citations
6.
Levin, Michael, Arnab Chatterjee, Antonella Pragliola, et al.. (1996). A comparative transcription map of the murine bare patches (Bpa) and striated (Str) critical regions and human Xq28.. Genome Research. 6(6). 465–477. 36 indexed citations
7.
Schindelhauer, Dirk, Heide Hellebrand, Ingrid Bader, et al.. (1996). Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich interval.. Genome Research. 6(11). 1056–1069. 24 indexed citations
8.
Schröder, W., et al.. (1996). Large-Scale Screening for Factor V Leiden Mutation in a North-Eastern German Population. Pathophysiology of Haemostasis and Thrombosis. 26(5). 233–236. 26 indexed citations
9.
Zhuchenko, Olga, et al.. (1996). Isolation, Mapping, and Genomic Structure of an X-Linked Gene for a Subunit of Human Mitochondrial Complex I. Genomics. 37(3). 281–288. 45 indexed citations
10.
Schröder, W., et al.. (1996). Intron 22 of factor VIII gene--a hot spot for structural aberrations causing severe hemophilia A [letter]. Blood. 87(7). 3067–3068. 8 indexed citations
11.
Reiner, Orly, Ying H. Shen, M Wehnert, et al.. (1993). Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats. Nature. 364(6439). 717–721. 824 indexed citations breakdown →
12.
Wehnert, M, Orly Reiner, & C. Thomas Caskey. (1993). Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134. Human Molecular Genetics. 2(9). 1503–1503. 21 indexed citations
13.
Wehnert, M, et al.. (1990). Genomic diagnosis of haemophilia A and B in the German Democratic Republic.. PubMed. 117(4). 601–7. 2 indexed citations
14.
Wehnert, M, et al.. (1990). A new marker at DXS 115 useful for carrier detection in hemophilia A. Human Genetics. 86(1). 59–60. 2 indexed citations
15.
Wehnert, M, et al.. (1989). Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia A.. PubMed. 7(2). 113–7. 10 indexed citations
16.
Herrmann, F. H., et al.. (1988). First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDR.. PubMed. 115(4). 489–93. 1 indexed citations
17.
Petruschka, Lothar, et al.. (1983). Reliability of the T�nnesen technique for the identification of Hunter carriers. Human Genetics. 64(4). 404–406. 3 indexed citations
18.
Wehnert, M, et al.. (1975). Vitamin B12-abhängige Methioninbiosynthese beiPseudomonas aeruginosa. Journal of Basic Microbiology. 15(4). 281–286. 4 indexed citations
19.
Wehnert, M, et al.. (1975). Vitamin B12‐abhängige Methioninbiosynthese bei Pseudomonas aeruginosa. Zeitschrift für allgemeine Mikrobiologie. 15(4). 281–286. 3 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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