Monika Cohen

3.3k total citations
13 papers, 859 citations indexed

About

Monika Cohen is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Monika Cohen has authored 13 papers receiving a total of 859 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Monika Cohen's work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Chromosomal and Genetic Variations (3 papers). Monika Cohen is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Chromosomal and Genetic Variations (3 papers). Monika Cohen collaborates with scholars based in Germany, United States and Netherlands. Monika Cohen's co-authors include Peter Wieacker, Sibylle Jakubiczka, Petra Muschke, Hannelore Thiele, Ralf H. Adams, Ilse Wieland, Klaus Gerlach, André Reis, Alexander Dreweke and Thomy de Ravel and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Monika Cohen

12 papers receiving 837 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Monika Cohen Germany	11	551	488	113	98	84	13	859
Karen Buysse Belgium	15	456 0.8×	633 1.3×	75 0.7×	169 1.7×	75 0.9×	19	959
Ute Grasshoff Germany	12	463 0.8×	477 1.0×	70 0.6×	100 1.0×	91 1.1×	29	791
Carmen Orellana Spain	19	440 0.8×	400 0.8×	57 0.5×	115 1.2×	68 0.8×	65	828
A. Moncla France	17	633 1.1×	748 1.5×	97 0.9×	174 1.8×	70 0.8×	29	1.1k
Alexandra Afenjar France	16	521 0.9×	621 1.3×	106 0.9×	113 1.2×	36 0.4×	42	1.0k
Suneeta Madan‐Khetarpal United States	15	430 0.8×	521 1.1×	70 0.6×	95 1.0×	72 0.9×	38	797
Karen M. Lower Australia	15	625 1.1×	400 0.8×	91 0.8×	53 0.5×	34 0.4×	34	927
Nathalie Van der Aa Belgium	19	412 0.7×	388 0.8×	84 0.7×	38 0.4×	47 0.6×	26	809
Gabriele Gillessen‐Kaesbach Germany	15	337 0.6×	471 1.0×	84 0.7×	152 1.6×	56 0.7×	23	753
Aimee S. Spikes United States	9	326 0.6×	452 0.9×	102 0.9×	79 0.8×	94 1.1×	11	598

Countries citing papers authored by Monika Cohen

Since Specialization

Citations

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

Fields of papers citing papers by Monika Cohen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monika Cohen

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

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Dincer, Yasemin, Julian Schulz, Monika Cohen, et al.. (2018). Multiple Integration and Data Annotation Study (MIDAS): improving next-generation sequencing data analysis by genotype-phenotype correlations. LaboratoriumsMedizin. 42(1-2). 1–8. 2 indexed citations

Schossig, Anna, Agnès Bloch‐Zupan, Adrian Lussi, et al.. (2016). SLC13A5 is the second gene associated with Kohlschütter–Tönz syndrome. Journal of Medical Genetics. 54(1). 54–62. 40 indexed citations

Huang, Lingli, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, et al.. (2012). A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability. The American Journal of Human Genetics. 91(4). 694–702. 73 indexed citations

Mencarelli, Maria Antonietta, Tjitske Kleefstra, Eleni Katzaki, et al.. (2009). 14q12 Microdeletion syndrome and congenital variant of Rett syndrome. European Journal of Medical Genetics. 52(2-3). 148–152. 28 indexed citations

Zweier, Christiane, Maarit Peippo, Juliane Hoyer, et al.. (2007). Haploinsufficiency of TCF4 Causes Syndromal Mental Retardation with Intermittent Hyperventilation (Pitt-Hopkins Syndrome). The American Journal of Human Genetics. 80(5). 994–1001. 215 indexed citations

Schell-Apacik, Chayim, Monika Cohen, Birgit Ertl‐Wagner, et al.. (2007). Gomez-Lopez-Hernandez syndrome (cerebello-trigeminal-dermal dysplasia): description of an additional case and review of the literature. European Journal of Pediatrics. 167(1). 123–126. 18 indexed citations

Hehr, Ute, Goekhan Uyanik, Claudia Groß, et al.. (2007). Novel POMGnT1 mutations define broader phenotypic spectrum of muscle–eye–brain disease. Neurogenetics. 8(4). 279–288. 41 indexed citations

Hoffmann, Katrin, Juliane Müller, Sigmar Stricker, et al.. (2006). Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit. The American Journal of Human Genetics. 79(2). 303–312. 100 indexed citations

Bisgaard, Anne‐Marie, Maria Kirchhoff, Zeynep Tümer, et al.. (2006). Additional chromosomal abnormalities in patients with a previously detected abnormal karyotype, mental retardation, and dysmorphic features. American Journal of Medical Genetics Part A. 140A(20). 2180–2187. 47 indexed citations

10.

Wieland, Ilse, Sibylle Jakubiczka, Petra Muschke, et al.. (2004). Mutations of the Ephrin-B1 Gene Cause Craniofrontonasal Syndrome. The American Journal of Human Genetics. 74(6). 1209–1215. 178 indexed citations

11.

Varon, Raymonda, Denise Horn, Monika Cohen, et al.. (2004). SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome. Human Genetics. 114(6). 553–561. 41 indexed citations

12.

Möhrenschlager, Matthias, William B. Rizzo, Cornelia Kraus, et al.. (2000). Sjörgen-Larsson-Syndrom. Der Hautarzt. 51(4). 250–255. 4 indexed citations

13.

Uhrig, Sabine, Simone Schuffenhauer, Christine Fauth, et al.. (1999). Multiplex-FISH for Pre- and Postnatal Diagnostic Applications. The American Journal of Human Genetics. 65(2). 448–462. 72 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.

Explore authors with similar magnitude of impact