A.M.A. Lachmeijer

644 total citations
7 papers, 329 citations indexed

About

A.M.A. Lachmeijer is a scholar working on Surgery, Molecular Biology and Obstetrics and Gynecology. According to data from OpenAlex, A.M.A. Lachmeijer has authored 7 papers receiving a total of 329 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Surgery, 2 papers in Molecular Biology and 2 papers in Obstetrics and Gynecology. Recurrent topics in A.M.A. Lachmeijer's work include Pregnancy and preeclampsia studies (2 papers), Dermatological and Skeletal Disorders (1 paper) and Genetic Syndromes and Imprinting (1 paper). A.M.A. Lachmeijer is often cited by papers focused on Pregnancy and preeclampsia studies (2 papers), Dermatological and Skeletal Disorders (1 paper) and Genetic Syndromes and Imprinting (1 paper). A.M.A. Lachmeijer collaborates with scholars based in Netherlands, Germany and France. A.M.A. Lachmeijer's co-authors include Hreinn Stefánsson, Reynir Tómas Geirsson, Reynir Arngrı́msson, Dan L. Nicolae, Jeffrey R. Gulcher, Bernhard Ø. Palsson, Augustine Kong, Birkir Þór Bragason, Michael L. Frigge and Ragnheiður I. Bjarnadóttir and has published in prestigious journals such as Human Molecular Genetics, Obstetrics and Gynecology and Journal of Medical Genetics.

In The Last Decade

A.M.A. Lachmeijer

7 papers receiving 316 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A.M.A. Lachmeijer Netherlands 6 153 153 102 76 71 7 329
Larissa Seidmann Germany 12 164 1.1× 85 0.6× 224 2.2× 111 1.5× 35 0.5× 31 427
B Robert United States 4 30 0.2× 43 0.3× 274 2.7× 29 0.4× 64 0.9× 4 364
Xin Dong China 10 78 0.5× 194 1.3× 90 0.9× 12 0.2× 72 1.0× 18 351
Anna‐Carina Weiss Germany 12 78 0.5× 13 0.1× 379 3.7× 66 0.9× 26 0.4× 23 468
Cheryl C. Y. Li Australia 7 79 0.5× 36 0.2× 314 3.1× 26 0.3× 27 0.4× 7 420
Henrik Jörnvall Sweden 8 22 0.1× 21 0.1× 473 4.6× 76 1.0× 44 0.6× 20 581
Beth A. Lubeck United States 7 23 0.2× 31 0.2× 132 1.3× 20 0.3× 41 0.6× 9 339
Jamie C. Wikenheiser United States 9 19 0.1× 16 0.1× 233 2.3× 62 0.8× 16 0.2× 11 344
Helen H. Kim United States 9 18 0.1× 17 0.1× 95 0.9× 69 0.9× 19 0.3× 15 305
Vittor Cândido Soares United States 2 90 0.6× 12 0.1× 418 4.1× 79 1.0× 10 0.1× 3 447

Countries citing papers authored by A.M.A. Lachmeijer

Since Specialization
Citations

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

Fields of papers citing papers by A.M.A. Lachmeijer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A.M.A. Lachmeijer

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

All Works

7 of 7 papers shown
1.
Revençu, Nicole, Laurence M. Boon, A. Dompmartin, et al.. (2013). Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth. Molecular Syndromology. 4(4). 173–178. 29 indexed citations
2.
Putoux, Audrey, Soumaya Mougou-Zerelli, Sophie Thomas, et al.. (2010). BBS10 mutations are common in ‘Meckel’-type cystic kidneys. Journal of Medical Genetics. 47(12). 848–852. 20 indexed citations
3.
Perdu, Bram, Phillis Lakeman, Geert Mortier, et al.. (2010). Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis. Clinical Genetics. 80(4). 383–388. 22 indexed citations
4.
Najm, Juliane, A.M.A. Lachmeijer, László Sztriha, et al.. (2008). Refining the phenotype of α‐1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly. Clinical Genetics. 74(5). 425–433. 67 indexed citations
5.
Lachmeijer, A.M.A.. (2001). Polymorphisms in the tumor necrosis factor and lymphotoxin-α gene region and preeclampsia. Obstetrics and Gynecology. 98(4). 612–619. 31 indexed citations
6.
Arngrı́msson, Reynir, Michael L. Frigge, Ragnheiður I. Bjarnadóttir, et al.. (1999). A Genome-Wide Scan Reveals a Maternal Susceptibility Locus for Pre-Eclampsia on Chromosome 2p13. Human Molecular Genetics. 8(9). 1799–1805. 156 indexed citations
7.
Geijn, Herman P. van, et al.. (1993). European multicentre studies in the field of Obstetrics. European Journal of Obstetrics & Gynecology and Reproductive Biology. 50(1). 5–23. 4 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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