Christina Evers

1.8k total citations
33 papers, 743 citations indexed

About

Christina Evers is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Christina Evers has authored 33 papers receiving a total of 743 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 18 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Christina Evers's work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Christina Evers is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Christina Evers collaborates with scholars based in Germany, Poland and United States. Christina Evers's co-authors include John A. Blessing, Edgardo Yordan, J.T. Thigpen, Linda F. Carson, Philip J. DiSaia, Katrin Hinderhofer, Ute Moog, Martin Granzow, Nagarajan Paramasivam and Christine Fischer and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Christina Evers

32 papers receiving 722 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christina Evers Germany	16	293	274	114	110	103	33	743
Herman Van den Berghe Belgium	10	302 1.0×	89 0.3×	111 1.0×	71 0.6×	80 0.8×	12	708
L A Brueton United Kingdom	19	728 2.5×	693 2.5×	27 0.2×	163 1.5×	154 1.5×	25	1.3k
J. Conny van Munsteren Netherlands	11	256 0.9×	85 0.3×	66 0.6×	25 0.2×	109 1.1×	12	539
Sean Young Canada	13	261 0.9×	201 0.7×	38 0.3×	285 2.6×	28 0.3×	27	736
Marga Schepens Netherlands	14	539 1.8×	336 1.2×	26 0.2×	76 0.7×	83 0.8×	20	779
Malwina Suszyńska United States	20	567 1.9×	133 0.5×	17 0.1×	152 1.4×	132 1.3×	42	1.1k
Valeria Vincenti Italy	5	586 2.0×	52 0.2×	166 1.5×	163 1.5×	54 0.5×	6	860
Haim Biran Israel	15	260 0.9×	129 0.5×	35 0.3×	200 1.8×	58 0.6×	40	841
Mina Takahashi Japan	12	407 1.4×	70 0.3×	32 0.3×	193 1.8×	73 0.7×	48	719
Arseni Markoff Germany	18	611 2.1×	319 1.2×	212 1.9×	43 0.4×	21 0.2×	49	1.1k

Countries citing papers authored by Christina Evers

Since Specialization

Citations

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

Fields of papers citing papers by Christina Evers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christina Evers

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

All Works

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20 of 20 papers shown

Evers, Christina, et al.. (2023). Compilation of Genotype and Phenotype Data in GCDH-LOVD for Variant Classification and Further Application. Genes. 14(12). 2218–2218. 1 indexed citations

Ott, Tim, Lilian Kaufmann, Martin Granzow, et al.. (2019). The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1. Frontiers in Physiology. 10. 134–134. 14 indexed citations

Evers, Christina, Christian Staufner, Martin Granzow, et al.. (2017). Impact of clinical exomes in neurodevelopmental and neurometabolic disorders. Molecular Genetics and Metabolism. 121(4). 297–307. 34 indexed citations

Schott, Sarah, Monika Keller, Thomas Brückner, et al.. (2017). Women at familial risk of breast cancer electing for prophylactic mastectomy: frequencies, procedures, and decision-making characteristics. Archives of Gynecology and Obstetrics. 295(6). 1451–1458. 7 indexed citations

Evers, Christina, Christine Fischer, Nicola Dikow, & Sarah Schott. (2017). Familial breast cancer: Genetic counseling over time, including patients´ expectations and initiators considering the Angelina Jolie effect. PLoS ONE. 12(5). e0177893–e0177893. 10 indexed citations

Keller, Monika, Thomas Brückner, Michael Golatta, et al.. (2016). Adherence to the breast cancer surveillance program for women at risk for familial breast and ovarian cancer versus overscreening: a monocenter study in Germany. Breast Cancer Research and Treatment. 156(2). 289–299. 21 indexed citations

Evers, Christina, Nagarajan Paramasivam, Katrin Hinderhofer, et al.. (2015). SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract. European Journal of Human Genetics. 23(12). 1627–1633. 15 indexed citations

Granzow, Martin, Nagarajan Paramasivam, Katrin Hinderhofer, et al.. (2015). Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline. Molecular and Cellular Probes. 29(5). 323–329. 20 indexed citations

Rump, Patrick, Nicole de Leeuw, Anthonie J. van Essen, et al.. (2014). Central 22q11.2 deletions. American Journal of Medical Genetics Part A. 164(11). 2707–2723. 43 indexed citations

10.

Evers, Christina, Anna Jauch, Johannes W.G. Janssen, et al.. (2014). Mosaic deletion of EXOC6B: Further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability. American Journal of Medical Genetics Part A. 164(12). 3088–3094. 15 indexed citations

11.

Bauer, Ralf, Nicola Dikow, Andreas Bräuer, et al.. (2014). The “Wagshurst study”: p.Val40Ile transthyretin gene variant causes late-onset cardiomyopathy. Amyloid. 21(4). 267–275. 10 indexed citations

12.

Evers, Christina, et al.. (2012). Integrated multiplex ligation dependent probe amplification (MLPA) assays for the detection of alterations in the HEXB, GM2A and SMARCAL1 genes to support the diagnosis of Morbus Sandhoff, M. Tay-Sachs variant AB and Schimke immuno-osseous dysplasia in humans. Molecular and Cellular Probes. 27(1). 32–37. 3 indexed citations

13.

Kloor, Matthias, Anita Y. Voigt, Christina Evers, et al.. (2012). The molecular basis of EPCAM expression loss in Lynch syndrome-associated tumors. Modern Pathology. 25(6). 911–916. 44 indexed citations

14.

Rath, M, Anne Langheinz, Sandrine Tchatchou, et al.. (2012). Molecular and clinical characterization of an in frame deletion of uncertain clinical significance in the BRCA2 gene. Breast Cancer Research and Treatment. 133(2). 725–734. 1 indexed citations

15.

Thiel, Anne, Manfred Beier, Kati Servan, et al.. (2011). Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance. Leukemia. 25(3). 387–399. 46 indexed citations

16.

Evers, Christina, P. Heidemann, Désirée Dunstheimer, et al.. (2010). Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?. Clinical Genetics. 79(5). 489–494. 7 indexed citations

17.

Ghadjar, Pirus, Mathew Simcock, Yitzhak Zimmer, et al.. (2010). Incidence of Small Lymph Node Metastases With Evidence of Extracapsular Extension: Clinical Implications in Patients With Head and Neck Squamous Cell Carcinoma. International Journal of Radiation Oncology*Biology*Physics. 78(5). 1366–1372. 18 indexed citations

18.

Evers, Christina, Barbara E. Lippok, Rudolf Volkmer, et al.. (2008). Box 2 Region of the Oncostatin M Receptor Determines Specificity for Recruitment of Janus Kinases and STAT5 Activation. Journal of Biological Chemistry. 283(28). 19465–19477. 30 indexed citations

19.

Evers, Christina, Manfred Beier, Barbara Hildebrandt, et al.. (2007). Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH. Genes Chromosomes and Cancer. 46(12). 1119–1128. 36 indexed citations

20.

Thigpen, J.T., John A. Blessing, Philip J. DiSaia, et al.. (1994). A randomized comparison of doxorubicin alone versus doxorubicin plus cyclophosphamide in the management of advanced or recurrent endometrial carcinoma: A Gynecologic Oncology Group study.. Journal of Clinical Oncology. 12(7). 1408–1414. 128 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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