Eric Haan

21.3k total citations · 1 hit paper
185 papers, 7.3k citations indexed

About

Eric Haan is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Eric Haan has authored 185 papers receiving a total of 7.3k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Genetics, 61 papers in Molecular Biology and 48 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Eric Haan's work include Prenatal Screening and Diagnostics (22 papers), Genomic variations and chromosomal abnormalities (19 papers) and Metabolism and Genetic Disorders (19 papers). Eric Haan is often cited by papers focused on Prenatal Screening and Diagnostics (22 papers), Genomic variations and chromosomal abnormalities (19 papers) and Metabolism and Genetic Disorders (19 papers). Eric Haan collaborates with scholars based in Australia, United States and United Kingdom. Eric Haan's co-authors include Annabelle Chan, Kevin Priest, Heather Scott, Phillipa van Essen, Alastair H. MacLennan, Vivienne Moore, Michael J. Davies, Kristyn Willson, Catherine Gibson and David F. Callen and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Eric Haan

184 papers receiving 7.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Reproductive Technologies and the Risk of Birth Defects

2012 553 citations Kevin Priest, Heather Scott et al. profile →

Peers

Countries citing papers authored by Eric Haan

Since Specialization

Citations

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

Fields of papers citing papers by Eric Haan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Haan

This figure shows the co-authorship network connecting the top 25 collaborators of Eric Haan. A scholar is included among the top collaborators of Eric 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 Eric Haan. Eric 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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20 of 20 papers shown

#	Work	Indexed citations
1	Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndrome 2015 ·European Journal of Medical Genetics ·Marie Shaw, (unknown), Lyndal Henden, Melanie Bahlo, Alison Gardner, Vera M. Kalscheuer, Eric Haan, Louise Christie, Anna Hackett, Jozef Gécz	13
2	Human Genetics Society of Australasia Position Statement: Population-Based Carrier Screening for Cystic Fibrosis 2014 ·Twin Research and Human Genetics ·Martin B. Delatycki, Jo Burke, Louise Christie, Felicity Collins, Michael T. Gabbett, Peter M. George, Eric Haan, Liane Ioannou, (unknown), Fiona McKenzie, Peter O’Leary, (unknown), Gillian Turner, John Massie	15
3	Non-coding VMA21 deletions cause X-linked Myopathy with Excessive Autophagy 2014 ·Neuromuscular Disorders ·Alessandra Ruggieri, N. Ramachandran, (unknown), Eric Haan, Christopher Kneebone, Jim Manavis, Lucía Morandi, Isabella Moroni, Peter Blumbergs, Marina Mora, Berge A. Minassian	24
4	Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase 2013 ·The American Journal of Human Genetics ·Philippe M. Campeau, Guy M. Lenk, (unknown), Yangjin Bae, Lindsay C. Burrage, Peter D. Turnpenny, Jorge Román Corona‐Rivera, Lucía Morandi, Marina Mora, Heiko Reutter, Anneke T. Vulto-van Silfhout, Laurence Faivre, Eric Haan, Richard A. Gibbs, (unknown), (unknown)	115
5	Lung disease associated with periventricular nodular heterotopia and an FLNA mutation 2010 ·European Journal of Medical Genetics ·Alice Masurel‐Paulet, Eric Haan, Elizabeth M. Thompson, Cyril Goizet, Christel Thauvin‐Robinet, Andrew W. Tai, Declan Kennedy, Greg Smith, T. Yee Khong, Guilhem Solé, (unknown), Isabelle Coupry, Frédéric Huet, Stephen P. Robertson, Laurence Faivre	47
6	Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2 2009 ·The Journal of Pediatrics ·Arash Ghalamkarpour, Christian Debauche, Eric Haan, Nicole Van Regemorter, Yves Sznajer, (unknown), Nicole Revençu, Y. Gillerot, Laurence M. Boon, Miikka Vikkula	29
7	Direct molecular diagnosis of myotonic dystrophy 2008 ·Clinical Genetics ·(unknown), Andrew J. Donnelly, Ági K. Gedeon, Roger W. Byard, Eric Haan, (unknown)	8
8	Association between Apolipoprotein E genotype and cerebral palsy is not confirmed in a Caucasian population 2008 ·Human Genetics ·G. McMichael, Catherine Gibson, Paul N. Goldwater, Eric Haan, Kevin Priest, Gustaaf Dekker, Alastair H. MacLennan	30
9	Associations between fetal inherited thrombophilia and adverse pregnancy outcomes 2006 ·American Journal of Obstetrics and Gynecology ·Catherine Gibson, Alastair H. MacLennan, Nard G. Janssen, Willem J. Kist, William M. Hague, Eric Haan, Paul N. Goldwater, Kevin Priest, Gustaaf Dekker	28
10	FBN1, TGFBR1, and the Marfan‐craniosynostosis/mental retardation disorders revisited 2006 ·American Journal of Medical Genetics Part A ·Lesley C. Adès, Kathleen E. Sullivan, Andrew Biggin, Eric Haan, Maggie Brett, Katherine Holman, Joanne Dixon, Stephen P. Robertson, Anthony D. Holmes, John Rogers, Bruce Bennetts	69
11	Health professionals' knowledge, practice and opinions about fetal alcohol syndrome and alcohol consumption in pregnancy 2005 ·Australian and New Zealand Journal of Public Health ·Jan Payne, Elizabeth Elliott, (unknown), Colleen O’Leary, (unknown), Eric Haan, C Bower	121
12	The prevalence of inherited thrombophilias in a Caucasian Australian population 2005 ·Pathology ·Catherine Gibson, Alastair H. MacLennan, Zbigniew Rudzki, William M. Hague, Eric Haan, (unknown), Kevin Priest, Annabelle Chan, Gustaaf Dekker, Paul N. Goldwater, T. Yee Khong, Mark R. Morton, Enzo Ranieri, Heather Scott, Heather Tapp, G. Casey	21
13	The Risk of Mortality or Cerebral Palsy in Twins: A Collaborative Population-Based Study 2002 ·Pediatric Research ·I Scher, (unknown), Eve Blair, Jonas H. Ellenberg, (unknown), Eric Haan, Dinah Reddihough, Marshalyn Yeargin‐Allsopp, Karin B. Nelson	173
14	Karyotypes found in the population declared at increased risk of Down syndrome following maternal serum screening 2001 ·Prenatal Diagnosis ·Richard Ryall, David F. Callen, (unknown), (unknown), (unknown), (unknown), (unknown), Eric Haan, (unknown), Grant Sutherland, D.W.P. Thomas, F. C. Webb	31
15	Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent 1999 ·Clinical Dysmorphology ·(unknown), Roger P. Davies, Eric Haan, Katherine Holman, (unknown), (unknown), (unknown), Dianna M. Milewicz, John F. Bateman, (unknown), Michael R. Eccles, (unknown), Michael Harbord	15
16	X‐inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation 1999 ·Clinical Genetics ·Hayley Woffendin, (unknown), Monique Jouet, Helen Stewart, Sarah Landy, Eric Haan, Ann Harris, Dian Donnai, Andrew Read, (unknown)	14
17	FIRST-TRIMESTER DIAGNOSIS OF SMITH–LEMLI–OPITZ SYNDROME 1997 ·Prenatal Diagnosis ·P. Sharp, Eric Haan, Janice M. Fletcher, T. Yee Khong, W.F. Carey	30
18	Hydrometrocolpos and segmental colonic dilatation in a girl with megacystis‐microcolon‐intestinal hypoperistalsis syndrome 1995 ·Journal of Paediatrics and Child Health ·(unknown), Nancy J. Brown, (unknown), (unknown), Eric Haan, Roger W. Byard, (unknown)	8
19	Nevoid basal cell carcinoma syndrome: Review of 118 affected individuals 1994 ·American Journal of Medical Genetics ·Susan Shanley, John W. Ratcliffe, Athel Hockey, Eric Haan, Christine Oley, David Ravine, Nicholas G. Martin, Carol Wicking, Georgia Chenevix‐Trench	250
20	New disorders of neurometabolism: When and how to investigate them 1988 ·Journal of Paediatrics and Child Health ·Eric Haan	2

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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