Annelyse Mertz

1.4k total citations · 1 hit paper
9 papers, 947 citations indexed

About

Annelyse Mertz is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Annelyse Mertz has authored 9 papers receiving a total of 947 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Cancer Research. Recurrent topics in Annelyse Mertz's work include CRISPR and Genetic Engineering (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Pluripotent Stem Cells Research (2 papers). Annelyse Mertz is often cited by papers focused on CRISPR and Genetic Engineering (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Pluripotent Stem Cells Research (2 papers). Annelyse Mertz collaborates with scholars based in Germany, United States and France. Annelyse Mertz's co-authors include Gudrun Rappold, M. Winkelmann, Ercole Rao, Maki Fukami, Tsutomu Ogata, U. Heinrich, Stefan Kirsch, Beate Niesler, André Rosenthal and Birgit Weiß and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Cell Death and Differentiation.

In The Last Decade

Annelyse Mertz

9 papers receiving 917 citations

Hit Papers

Pseudoautosomal deletions... 1997 2026 2006 2016 1997 200 400 600
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. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
    1997 701 citations Ercole Rao, Birgit Weiß et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Annelyse Mertz Germany 9 752 663 174 130 89 9 947
M. Winkelmann Germany 7 739 1.0× 638 1.0× 162 0.9× 127 1.0× 88 1.0× 7 923
Ercole Rao Germany 12 777 1.0× 763 1.2× 178 1.0× 144 1.1× 65 0.7× 19 1.1k
Simone Schiller Germany 6 393 0.5× 307 0.5× 65 0.4× 51 0.4× 25 0.3× 8 507
Birgit Schechinger Germany 6 218 0.3× 246 0.4× 55 0.3× 32 0.2× 70 0.8× 8 519
M. G. Daker United Kingdom 13 333 0.4× 225 0.3× 113 0.6× 15 0.1× 47 0.5× 28 538
Jean Pierre Siffroi France 16 483 0.6× 387 0.6× 93 0.5× 8 0.1× 376 4.2× 35 792
Huntington F. Willard United States 11 309 0.4× 397 0.6× 196 1.1× 12 0.1× 8 0.1× 14 591
Carolina Sismani Cyprus 19 735 1.0× 515 0.8× 184 1.1× 6 0.0× 105 1.2× 75 984
Ada Rosenmann Israel 16 252 0.3× 347 0.5× 108 0.6× 8 0.1× 51 0.6× 36 650
Claude‐Lise Richer Canada 15 397 0.5× 458 0.7× 194 1.1× 6 0.0× 68 0.8× 35 759

Countries citing papers authored by Annelyse Mertz

Since Specialization
Citations

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

Fields of papers citing papers by Annelyse Mertz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annelyse Mertz

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

All Works

9 of 9 papers shown
1.
Codner, Gemma, Adam Caulder, Marie Wattenhofer‐Donzé, et al.. (2016). Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction. BMC Cell Biology. 17(1). 30–30. 20 indexed citations
2.
Duval, David, Marina Trouillas, Christelle Thibault-Carpentier, et al.. (2005). Apoptosis and differentiation commitment: novel insights revealed by gene profiling studies in mouse embryonic stem cells. Cell Death and Differentiation. 13(4). 564–575. 48 indexed citations
3.
Schiebel, K., M. Winkelmann, Annelyse Mertz, et al.. (1997). Abnormal XY Interchange between a Novel Isolated Protein Kinase Gene, PRKY, and Its Homologue, PRKX, Accounts for One Third of All (Y+)XX Males and (Y-)XY Females. Human Molecular Genetics. 6(11). 1985–1989. 95 indexed citations
4.
Rao, Ercole, Maki Fukami, Annelyse Mertz, et al.. (1997). FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes. Human Genetics. 100(2). 236–239. 21 indexed citations
5.
Spranger, Stephanie, Stefan Kirsch, Annelyse Mertz, et al.. (1997). Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal height. Clinical Genetics. 51(5). 346–350. 10 indexed citations
6.
Schiebel, K., Annelyse Mertz, M. Winkelmann, et al.. (1997). FISH localization of the human Y-homolog of protein kinase PRKX (PRKY) to Yp11.2 and two pseudogenes to 15q26 and Xq12→q13. Cytogenetic and Genome Research. 76(1-2). 49–52. 19 indexed citations
7.
Rao, Ercole, Birgit Weiß, Maki Fukami, et al.. (1997). Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nature Genetics. 16(1). 54–63. 701 indexed citations breakdown →
8.
Ried, Karin, Annelyse Mertz, Ramaiah Nagaraja, et al.. (1995). Characterization of a YAC Contig Spanning the Pseudoautosomal Region. Genomics. 29(3). 787–792. 20 indexed citations
9.
Schiebel, K., Annelyse Mertz, M. Winkelmann, Ramaiah Nagaraja, & Gudrun Rappold. (1994). Localization of the Adenine Nucleotide Translocase Gene ANT2 to Chromosome Xq24-q25 with Tight Linkage to DXS425. Genomics. 24(3). 605–606. 13 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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