Karen Marks

2.2k total citations
11 papers, 355 citations indexed

About

Karen Marks is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Karen Marks has authored 11 papers receiving a total of 355 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Surgery. Recurrent topics in Karen Marks's work include Prenatal Screening and Diagnostics (4 papers), Chromosomal and Genetic Variations (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Karen Marks is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Chromosomal and Genetic Variations (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Karen Marks collaborates with scholars based in United Kingdom, Poland and United States. Karen Marks's co-authors include P C Elwood, Freddy Sitas, M L Burr, D Forman, J. W. G. Yarnell, Michael A. Patton, Tracey A. Smith, Meaghan Wall, A.L. Muggleton-Harris and Dragana Josifova and has published in prestigious journals such as Gut, Scientific Reports and Human Reproduction.

In The Last Decade

Karen Marks

11 papers receiving 327 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karen Marks United Kingdom	7	184	98	66	61	57	11	355
I Nolte Netherlands	7	63 0.3×	42 0.4×	44 0.7×	69 1.1×	5 0.1×	19	257
Kyu Rae Kim South Korea	9	83 0.5×	30 0.3×	62 0.9×	109 1.8×	6 0.1×	14	330
Michael Fatouros Greece	9	88 0.5×	77 0.8×	50 0.8×	4 0.1×	32 0.6×	16	236
Ichiro Takeuchi Japan	10	74 0.4×	63 0.6×	68 1.0×	56 0.9×	16 0.3×	41	246
J. García‐Paredes Spain	8	79 0.4×	178 1.8×	43 0.7×	107 1.8×	17 0.3×	16	305
Yu Liang China	11	157 0.9×	32 0.3×	27 0.4×	72 1.2×	2 0.0×	29	379
Kara M. De Felice United States	6	59 0.3×	56 0.6×	21 0.3×	93 1.5×	21 0.4×	8	326
Neriman Sarı Türkiye	11	58 0.3×	47 0.5×	133 2.0×	13 0.2×	4 0.1×	31	342
Ryusuke Nambu Japan	10	100 0.5×	139 1.4×	39 0.6×	105 1.7×	33 0.6×	40	278
Claudine Le Vaillant France	12	51 0.3×	95 1.0×	73 1.1×	46 0.8×		45	400

Countries citing papers authored by Karen Marks

Since Specialization

Citations

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

Fields of papers citing papers by Karen Marks

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Marks

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

All Works

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11 of 11 papers shown

Marks, Karen, et al.. (2024). Selected somatic parameters and body composition as predictors of cardiorespiratory fitness among Polish adolescents aged 11–14. Scientific Reports. 14(1). 25355–25355. 1 indexed citations

Hanson, Helen, Meredith Wilson, John Short, et al.. (2014). Germline CBL mutation associated with a noonan‐like syndrome with primary lymphedema and teratoma associated with acquired uniparental isodisomy of chromosome 11q23. American Journal of Medical Genetics Part A. 164(4). 1003–1009. 23 indexed citations

Tatton‐Brown, Katrina, Daniela T. Pilz, Karen Helene Ørstavik, et al.. (2009). 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q. American Journal of Medical Genetics Part A. 149A(2). 147–154. 55 indexed citations

Chatzimeletiou, Katerina, Jon Taylor, Karen Marks, J.G. Grudzinskas, & Alan H. Handyside. (2006). Paternal inheritance of a 16qh- polymorphism in a patient with repeated IVF failure. Reproductive BioMedicine Online. 13(6). 864–867. 6 indexed citations

Josifova, Dragana, Michael A. Patton, & Karen Marks. (2004). Oculoauriculovertebral spectrum phenotype caused by an unbalanced t(5;8)(p15.31;p23.1) rearrangement. Clinical Dysmorphology. 13(3). 151–153. 23 indexed citations

Gibson, Frances M., et al.. (2002). Combined immunocytochemistry and FISH: an improved method to study engraftment of accessory bone marrow stromal cells. Clinical & Laboratory Haematology. 24(6). 329–335. 2 indexed citations

Scopes, John, et al.. (2001). Correction of stromal cell defect after bone marrow transplantation in aplastic anaemia. British Journal of Haematology. 115(3). 642–652. 22 indexed citations

Wall, Meaghan, et al.. (1996). Fertilization and early embryology: Cytogenetic and fluorescent in-situ hybridization chromosomal studies on in-vitro fertilized and intracytoplasmic sperm injected 'failed-fertilized' human oocytes. Human Reproduction. 11(10). 2230–2238. 50 indexed citations

Byrne, Dominic, et al.. (1995). First trimester amnifiltration: technical, cytogenetic and pregnancy outcome of 104 consecutive procedures. BJOG An International Journal of Obstetrics & Gynaecology. 102(3). 220–223. 2 indexed citations

10.

Sitas, Freddy, D Forman, J. W. G. Yarnell, et al.. (1991). Helicobacter pylori infection rates in relation to age and social class in a population of Welsh men.. Gut. 32(1). 25–28. 164 indexed citations

11.

Marks, Karen, et al.. (1985). Interstitial deletion of chromosome 7p detected antenatally.. Journal of Medical Genetics. 22(4). 316–318. 7 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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