E Haan

1.3k total citations
17 papers, 762 citations indexed

About

E Haan is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, E Haan has authored 17 papers receiving a total of 762 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in E Haan's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Chromosomal and Genetic Variations (3 papers). E Haan is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Chromosomal and Genetic Variations (3 papers). E Haan collaborates with scholars based in Australia, United States and Slovakia. E Haan's co-authors include David F. Callen, Helen J. Eyre, Elizabeth Elliott, Janet M Payne, Carol Bower, Anne Morris, G.R. Sutherland, Patrick J. Willems, Guus Hamers and Ági K. Gedeon and has published in prestigious journals such as Human Molecular Genetics, BJOG An International Journal of Obstetrics & Gynaecology and Archives of Disease in Childhood.

In The Last Decade

E Haan

17 papers receiving 730 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E Haan Australia	13	419	235	234	108	77	17	762
Kirsten Rasmussen Denmark	18	330 0.8×	252 1.1×	143 0.6×	110 1.0×	156 2.0×	44	977
Stuart W. Tinker United States	15	298 0.7×	283 1.2×	302 1.3×	58 0.5×	33 0.4×	15	776
J. P. Fryns Belgium	18	444 1.1×	377 1.6×	265 1.1×	44 0.4×	18 0.2×	69	1.3k
Tim Donlon United States	18	672 1.6×	607 2.6×	254 1.1×	80 0.7×	4 0.1×	26	1.3k
Harold Chen United States	19	514 1.2×	351 1.5×	203 0.9×	118 1.1×	9 0.1×	57	921
R. Douglas Wilson Canada	19	517 1.2×	259 1.1×	1.1k 4.6×	34 0.3×	197 2.6×	50	1.4k
E.J.T. Winsor Canada	20	450 1.1×	283 1.2×	596 2.5×	147 1.4×	87 1.1×	46	1.2k
Jon M. Aase United States	17	373 0.9×	205 0.9×	404 1.7×	39 0.4×	136 1.8×	27	1.1k
Mandakini Pradhan India	15	109 0.3×	81 0.3×	204 0.9×	14 0.1×	46 0.6×	71	722
Kristin M. May United States	13	461 1.1×	674 2.9×	359 1.5×	76 0.7×	9 0.1×	18	1.2k

Countries citing papers authored by E Haan

Since Specialization

Citations

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

Fields of papers citing papers by E Haan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E Haan

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

All Works

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17 of 17 papers shown

Hynes, Kim, Patrick Tarpey, Leanne M. Dibbens, et al.. (2009). Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families. Journal of Medical Genetics. 47(3). 211–216. 59 indexed citations

Talseth‐Palmer, Bente A., Nikola A. Bowden, Cliff Meldrum, et al.. (2009). A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology. Cytogenetic and Genome Research. 124(1). 94–101. 6 indexed citations

Haan, E, et al.. (2008). Fetal exposure to herpesviruses may be associated with pregnancy‐induced hypertensive disorders and preterm birth in a Caucasian population*. BJOG An International Journal of Obstetrics & Gynaecology. 115(4). 492–500. 51 indexed citations

Elliott, Elizabeth, Janet M Payne, Anne Morris, E Haan, & Carol Bower. (2007). Fetal alcohol syndrome: a prospective national surveillance study. Archives of Disease in Childhood. 93(9). 732–737. 94 indexed citations

Hasler, Carol, et al.. (2005). A South Australian population‐based study of congenital talipes equinovarus. Paediatric and Perinatal Epidemiology. 19(3). 227–237. 54 indexed citations

Yu, Shuancang, Elizabeth Baker, H.J. Eyre, et al.. (2005). Frequency of truly cryptic subtelomere abnormalities – a study of 534 patients and literature review. Clinical Genetics. 68(5). 436–441. 12 indexed citations

White, Susan M., Elizabeth M. Thompson, Alexa Kidd, et al.. (2004). Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa–Kuroki) syndrome. American Journal of Medical Genetics Part A. 127A(2). 118–127. 66 indexed citations

DuPont, Barbara R., et al.. (2004). The Hunter–McAlpine syndrome results from duplication 5q35–qter. Clinical Genetics. 67(1). 53–60. 11 indexed citations

Baker, Elizabeth, et al.. (2002). A familial cryptic subtelomeric deletion 12p with variable phenotypic effect. Clinical Genetics. 61(3). 198–201. 29 indexed citations

10.

Gécz, Jozef, B. A. Oostra, Athel Hockey, et al.. (1997). FMR2 Expression in Families with Fraxe Mental Retardation. Human Molecular Genetics. 6(3). 435–441. 45 indexed citations

11.

Lüdecke, H.-J., M.J. Wagner, Julia Parrish, et al.. (1995). Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer--Giedion syndrome. Human Molecular Genetics. 4(1). 31–36. 95 indexed citations

12.

Callen, David F., et al.. (1992). Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes. American Journal of Medical Genetics. 43(4). 709–715. 109 indexed citations

13.

Robertson, E. F., et al.. (1991). A maternal serum screen for trisomy 18: an extension of maternal serum screening for Down syndrome.. PubMed. 49(5). 1025–33. 33 indexed citations

14.

Staples, Alan, et al.. (1991). Epidemiology of Down syndrome in South Australia, 1960-89.. PubMed. 49(5). 1014–24. 32 indexed citations

15.

Trent, Ronald J., Francesca Volpato, Arabella Smith, et al.. (1991). Molecular and cytogenetic studies of the Prader-Willi syndrome.. Journal of Medical Genetics. 28(10). 649–654. 19 indexed citations

16.

Sutherland, G.R., et al.. (1988). Linkage studies with the gene for an X‐linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2). American Journal of Medical Genetics. 30(1-2). 493–508. 46 indexed citations

17.

Haan, E, et al.. (1988). Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.. PubMed. 24 Suppl 1. 92–7. 1 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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