E Haan

1.3k citations

17 papers · 762 indexed · h-index 13

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics
- Prenatal Substance Exposure Effects

Papers in ⓘ

Genetics 11
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 2
Obstetrics and Gynecology 2

Co-authors: David F. Callen (2 shared papers)Helen J. Eyre (1 shared paper)Elizabeth Elliott (1 shared paper)Janet M Payne (1 shared paper)Anne Morris (1 shared paper)Carol Bower (1 shared paper)G.R. Sutherland (2 shared papers)J.C. Mulley (1 shared paper)
Journals: Clinical Genetics (3 papers)Human Molecular Genetics (2 papers)Journal of Medical Genetics (2 papers)Archives of Disease in Childhood (1 paper)Paediatric and Perinatal Epidemiology (1 paper)
Partner nations: Australia United States Slovakia

In The Last Decade

E Haan

17 papers receiving 730 citations

Peers

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-authors

The 25 scholars most cited alongside E Haan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with E Haan Line = papers co-authored together E Haan links everyone, so they are left out of the graph.

All Works

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17 of 17 papers shown

#	Work
1	Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes American Journal of Medical Genetics ·David F. Callen, Helen J. Eyre, M‐Y Yip, J.B. Freemantle, E Haan	1992	109
2	Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer--Giedion syndrome Human Molecular Genetics ·H.-J. Lüdecke, M.J. Wagner, J. Nardmann, Biagio La Pillo, Julia Parrish, Patrick J. Willems, E Haan, Moshe Frydman, Guus Hamers, D. E.Weils, Bernhard Horsthemke	1995	95
3	Fetal alcohol syndrome: a prospective national surveillance study Archives of Disease in Childhood ·Elizabeth Elliott, Janet M Payne, Anne Morris, E Haan, Carol Bower	2007	94
4	Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa–Kuroki) syndrome American Journal of Medical Genetics Part A ·Susan M. White, Elizabeth M. Thompson, Alexa Kidd, Ravi Savarirayan, Anne Turner, David J. Amor, M. B. Delatycki, Michael Fahey, Anne Baxendale, (unknown), (unknown), E Haan, Kate Gibson, Jane Halliday, Agnes Bankier	2004	66
5	Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families Journal of Medical Genetics ·Kim Hynes, Patrick Tarpey, Leanne M. Dibbens, Marta A. Bayly, Samuel F. Berkovic, Roger Smith, Z. A. Raisi, Samantha J. Turner, Natasha J. Brown, Tarishi Desai, E Haan, G Turner, John Christodoulou, Helen Leonard, Deepak Gill, Michael R. Stratton, Jozef Gécz, Ingrid E. Scheffer	2009	59
6	A South Australian population‐based study of congenital talipes equinovarus Paediatric and Perinatal Epidemiology ·Rosemary Byron‐Scott, Phillipa Sharpe, Carol Hasler, Peter J. Cundy, Craig Hirte, Annabelle Chan, H. C. F. Scott, Peter Baghurst, E Haan	2005	54
7	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 ·C.F. Gibson, P N Goldwater, AH MacLennan, E Haan, Kevin Priest, GA Dekker	2008	51
8	Linkage studies with the gene for an X‐linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2) American Journal of Medical Genetics ·G.R. Sutherland, Ági K. Gedeon, E Haan, P. Woodroffe, J.C. Mulley	1988	46
9	FMR2 Expression in Families with Fraxe Mental Retardation Human Molecular Genetics ·Jozef Gécz, B. A. Oostra, Athel Hockey, Pablo Carbonell, Gillian Turner, E Haan, G.R. Sutherland, John C. Mulley	1997	45
10	A maternal serum screen for trisomy 18: an extension of maternal serum screening for Down syndrome. PubMed ·A J Staples, E. F. Robertson, Enzo Ranieri, Richard Ryall, E Haan	1991	33
11	Epidemiology of Down syndrome in South Australia, 1960-89. PubMed ·Alan Staples, G. R. Sutherland, E Haan, Suzanne Clisby	1991	32
12	A familial cryptic subtelomeric deletion 12p with variable phenotypic effect Clinical Genetics ·Elizabeth Baker, Lyn Hinton, David F. Callen, E Haan, Angus Dobbie, GR Sutherland	2002	29
13	Molecular and cytogenetic studies of the Prader-Willi syndrome. Journal of Medical Genetics ·Ronald J. Trent, Francesca Volpato, Arabella Smith, Robert W. Lindeman, Marty Kwok‐Shing Wong, Garry L. Warne, E Haan	1991	19
14	Frequency of truly cryptic subtelomere abnormalities – a study of 534 patients and literature review Clinical Genetics ·Shuancang Yu, Elizabeth Baker, Lyn Hinton, H.J. Eyre, Wendy Waters, Sarah J. Higgins, GR Sutherland, E Haan	2005	12
15	The Hunter–McAlpine syndrome results from duplication 5q35–qter Clinical Genetics ·AGW Hunter, Barbara R. DuPont, Margaret E. McLaughlin, Lyn Hinton, Elizabeth Baker, Lesley C. Adès, E Haan, CE Schwartz	2004	11
16	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 ·Bente A. Talseth‐Palmer, Nikola A. Bowden, Cliff Meldrum, J. Nicholl, Elizabeth Thompson, Kathryn Friend, Jan Liebelt, Drago Bratkovic, E Haan, S. Yu, Rodney J. Scott	2009	6
17	Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy. PubMed ·JC Mulley, Ak Gedeon, E Haan, Sheffield Lj, White Sj, Bates Lj, Robertson Ef, Sutherland Gr	1988	1

About E Haan

E Haan is a scholar working on Genetics, Obstetrics and Gynecology, Pediatrics, Perinatology and Child Health, Rehabilitation and Orthopedics and Sports Medicine, having authored 17 papers that have together received 762 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (3 papers), Parvovirus B19 Infection Studies (2 papers), Autism Spectrum Disorder Research (2 papers), Genomics and Chromatin Dynamics (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Genetics (419 citations), Pediatrics, Perinatology and Child Health (234 citations), Obstetrics and Gynecology (77 citations), Developmental Biology (16 citations) and Orthopedics and Sports Medicine (43 citations). E Haan has collaborated with scholars based in Australia, United States and Slovakia. Frequent co-authors include David F. Callen, Helen J. Eyre, Elizabeth Elliott, Janet M Payne, Anne Morris, Carol Bower, G.R. Sutherland, J.C. Mulley, Guus Hamers and Bernhard Horsthemke. Their work appears in journals such as Clinical Genetics, Human Molecular Genetics, Journal of Medical Genetics, Archives of Disease in Childhood and Paediatric and Perinatal Epidemiology.

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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