Ellen Markljung

503 total citations
15 papers, 312 citations indexed

About

Ellen Markljung is a scholar working on Surgery, Urology and Molecular Biology. According to data from OpenAlex, Ellen Markljung has authored 15 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Surgery, 7 papers in Urology and 6 papers in Molecular Biology. Recurrent topics in Ellen Markljung's work include Urological Disorders and Treatments (7 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Congenital gastrointestinal and neural anomalies (2 papers). Ellen Markljung is often cited by papers focused on Urological Disorders and Treatments (7 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Congenital gastrointestinal and neural anomalies (2 papers). Ellen Markljung collaborates with scholars based in Sweden, China and United Kingdom. Ellen Markljung's co-authors include Agneta Nordenskjöld, Yougen Chen, Leif Andersson, Johanna Lundin, Kristina Lagerstedt‐Robinson, Shengtian Zhao, Xu‐Feng Zhang, Nel Roeleveld, Tatjana Adamović and Iris A.L.M. van Rooij and has published in prestigious journals such as The Lancet, Nature Genetics and Nature Reviews Genetics.

In The Last Decade

Ellen Markljung

15 papers receiving 309 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ellen Markljung Sweden	11	146	123	122	97	29	15	312
Salvador Ramı́rez-Jiménez Mexico	9	153 1.0×	151 1.2×	22 0.2×	91 0.9×	19 0.7×	12	285
Michael W. Leihy Australia	10	281 1.9×	206 1.7×	96 0.8×	11 0.1×	19 0.7×	11	451
Denise R. Archambeault United States	8	196 1.3×	99 0.8×	24 0.2×	44 0.5×	13 0.4×	8	267
Lydia Ferguson United States	9	174 1.2×	146 1.2×	16 0.1×	113 1.2×	16 0.6×	14	362
Christian Høst Denmark	6	213 1.5×	258 2.1×	14 0.1×	35 0.4×	28 1.0×	7	400
Avenel Joseph United States	6	152 1.0×	115 0.9×	36 0.3×	25 0.3×	13 0.4×	6	322
L Dorantes Mexico	8	137 0.9×	238 1.9×	13 0.1×	319 3.3×	11 0.4×	13	431
Maha M. Eid Egypt	10	154 1.1×	92 0.7×	24 0.2×	22 0.2×	30 1.0×	52	318
Tossaporn Seeherunvong United States	7	131 0.9×	113 0.9×	29 0.2×	18 0.2×	15 0.5×	14	201
Ariella Weinberg‐Shukron Israel	9	229 1.6×	173 1.4×	14 0.1×	16 0.2×	55 1.9×	15	377

Countries citing papers authored by Ellen Markljung

Since Specialization

Citations

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

Fields of papers citing papers by Ellen Markljung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ellen Markljung

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

All Works

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15 of 15 papers shown

Bruhn‐Olszewska, Bożena, Ellen Markljung, Edyta Rychlicka-Buniowska, et al.. (2025). The effects of loss of Y chromosome on male health. Nature Reviews Genetics. 26(5). 320–335. 8 indexed citations

Lundin, Johanna, Ellen Markljung, Izabella Baranowska Körberg, et al.. (2019). Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate gene. Molecular Genetics & Genomic Medicine. 7(6). e666–e666. 5 indexed citations

Körberg, Izabella Baranowska, Wolfgang Hofmeister, Ellen Markljung, et al.. (2015). WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish. Human Molecular Genetics. 24(18). 5069–5078. 21 indexed citations

Söderhäll, Cilla, Izabella Baranowska Körberg, Jia Cao, et al.. (2014). Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias. European Journal of Human Genetics. 23(4). 516–522. 12 indexed citations

Granström, Anna Löf, Ellen Markljung, Katharina Fink, et al.. (2013). A novel stop mutation in the EDNRB gene in a family with Hirschsprung’s disease associated with Multiple Sclerosis. Journal of Pediatric Surgery. 49(4). 622–625. 8 indexed citations

Ka, Sojeong, Ellen Markljung, Frank W. Albert, et al.. (2013). Expression of carnitine palmitoyl-CoA transferase-1B is influenced by a cis-acting eQTL in two chicken lines selected for high and low body weight. Physiological Genomics. 45(9). 367–376. 12 indexed citations

Markljung, Ellen, Tatjana Adamović, Jia Cao, et al.. (2012). Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype. Gene. 507(1). 50–53. 14 indexed citations

Adamović, Tatjana, et al.. (2012). The p.G146A and p.P125P Polymorphisms in the Steroidogenic Factor-1 <b><i>(SF-1)</i></b> Gene Do Not Affect the Risk for Hypospadias in Caucasians. Sexual Development. 6(6). 292–297. 14 indexed citations

Markljung, Ellen, Tatjana Adamović, Lisa Örtqvist, Tomas Wester, & Agneta Nordenskjöld. (2012). A rare microduplication in a familial case of annular pancreas and duodenal stenosis. Journal of Pediatric Surgery. 47(11). 2039–2043. 5 indexed citations

10.

Zhang, Xufeng, et al.. (2011). Hypospadias associated with hypertelorism, the mildest phenotype of Opitz syndrome. The Lancet. 56(5). 348–351. 13 indexed citations

11.

Andersson, Leif, Göran Andersson, Göran Hjälm, et al.. (2010). ZBED6. Transcription. 1(3). 144–148. 17 indexed citations

12.

Chen, Yougen, Johanna Lundin, Kristina Lagerstedt‐Robinson, et al.. (2010). Mutational study of the MAMLD1-gene in hypospadias. European Journal of Medical Genetics. 53(3). 122–126. 39 indexed citations

13.

Zanden, Loes F.M. van der, Iris A.L.M. van Rooij, Wout Feitz, et al.. (2010). Common variants in DGKK are strongly associated with risk of hypospadias. Nature Genetics. 43(1). 48–50. 82 indexed citations

14.

Markljung, Ellen, Martin Braunschweig, Peter Karlskov‐Mortensen, et al.. (2008). Genome-wide identification of quantitative trait loci in a cross between Hampshire and Landrace II: Meat quality traits. BMC Genetics. 9(1). 22–22. 41 indexed citations

15.

Karlskov‐Mortensen, Peter, Milena Sawera, Ellen Markljung, et al.. (2005). Genome‐wide identification of quantitative trait loci in a cross between Hampshire and Landrace I: carcass traits. Animal Genetics. 37(2). 156–162. 21 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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