R.C.M. Hennekam

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R.C.M. Hennekam has published from 2000 upto 2015 at (or in association with) the University of Amsterdam (as found in the CRIS of the UvA for the years 2000 upto 2015 ) a total of 350 publications. The above histogram shows the different types and number of publications for this whole publication period at the University of Amsterdam.

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Complete publication type list

A picture is worth a thousand words, but the above histogram can be described by the following words: (not thousand but around 145 words, click 'view' button to show those words).
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In 2000 R.C.M. Hennekam published eleven articles. In 2001 R.C.M. Hennekam published ten articles. In 2002 R.C.M. Hennekam published eleven articles and published one chapter. In 2003 R.C.M. Hennekam published nineteen articles, published one chapter and gave his / her inaugural address. In 2004 R.C.M. Hennekam published sixteen articles. In 2005 R.C.M. Hennekam published thirty-nine articles. In 2006 R.C.M. Hennekam published fifteen articles. In 2007 R.C.M. Hennekam published twenty-one articles. In 2008 R.C.M. Hennekam published eightteen articles. In 2009 R.C.M. Hennekam published twenty-eight articles. In 2010 R.C.M. Hennekam published thirty-one articles and published two chapters. In 2011 R.C.M. Hennekam published twenty-six articles. In 2012 R.C.M. Hennekam published thirty-two articles. In 2013 R.C.M. Hennekam published twenty-two articles. In 2014 R.C.M. Hennekam published twenty-nine articles. In 2015 R.C.M. Hennekam published seventeen articles.

Mentions of publications by R.C.M. Hennekam on altmetric.com

We did find some data on societal impact for R.C.M. Hennekam on altmetric.com.
Data are collected on altmetic.com (September 2015) based on publications found in the CRIS of the UvA (march 2015 update). Only publications in 2013 and 2014 are harvested.

15 mentions of a publication in Lancet Neurology (2014).
The genetic basis of DOORS syndrome: an exome-sequencing study
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6 mentions of a publication in American Journal of Medical Genetics. Part A (2013).
Elements of Morphology: Standard Terminology for the External Genitalia
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5 mentions of a publication in Nature genetics (2014).
Mutations in ZBTB20 cause Primrose syndrome
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4 mentions of a publication in Human Mutation (2013).
Kohlschütter-Tönz syndrome: mutations in ROGDI and evidence of genetic heterogeneity
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4 mentions of a publication in Human Mutation (2013).
Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients
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3 mentions of a publication in Human Molecular Genetics (2014).
Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia
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3 mentions of a publication in Human Genetics (2014).
Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome
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3 mentions of a publication in Journal of Medical Genetics (2013).
High rate of mosaicism in individuals with Cornelia de Lange syndrome
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3 mentions of a publication in Neuropediatrics (2014).
Brain tumors and syndromes in children
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3 mentions of a publication in Journal of Medical Genetics (2013).
Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement
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2 mentions of a publication in American Journal of Medical Genetics. Part A (2014).
Eight Years Experience from a Skeletal Dysplasia Referral Center in a Tertiary Hospital in Southern India: A Model for the Diagnosis and Treatment of Rare Diseases in a Developing Country
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2 mentions of a publication in American Journal of Human Genetics (2013).
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
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2 mentions of a publication in Journal of Medical Genetics (2014).
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism
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2 mentions of a publication in American Journal of Medical Genetics. Part A (2013).
Diagnostic outcomes of 27 children referred by pediatricians to a genetics clinic in the Netherlands with suspicion of fetal alcohol spectrum disorders
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1 mentions of a publication in Circulation. Cardiovascular genetics (2013).
The cardiac phenotype in patients with a CHD7 mutation
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1 mentions of a publication in Journal of Investigative Dermatology (2014).
Retinitis pigmentosa, cutis laxa, and pseudoxanthoma elasticum-like skin manifestations associated with GGCX mutations
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1 mentions of a publication in American Journal of Medical Genetics. Part C: Seminars in Medical Genetics (2014).
Phenotype and genotype in Nicolaides-Baraitser syndrome
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1 mentions of a publication in American Journal of Medical Genetics. Part A (2014).
Growth Charts for Individuals with Rubinstein-Taybi Syndrome
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1 mentions of a publication in Journal of clinical endocrinology and metabolism (2013).
The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients
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1 mentions of a publication in American Journal of Medical Genetics. Part A (2013).
Intellectual disability and hemizygous GPD2 mutation
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Album Academicum profile

Professor Hennekam

First name(-s): Raoul Christiaan Marie
Professor Hennekam obtained his pHd in 1990
( ).

Narcis profile

Prof.dr. R.C.M. (Raoul) Hennekam

Smiley faceProfessor
249 Publications
Clinical genetics; Molecular genetics; Dysmorphology; Natural history syndromes; Congenital anomalies; Skeletal dysplasias; Connective tissue disorders; Mental retardation; Autism
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Journals and co-authors

Complete co-author list

Publishers

Complete publisher list

Write Position

R.C.M. Hennekam published from 2000 upto 2015 a total of 345 UvA-articles with 50 or less co-authors.
1843 unique co-authors in total with an average of 8.77 co-authors per article.

10 number of times sole author
6 number of times first author
14 number of times second author
149 number of times last author
Visualization of the write position of the 345 journal publications by R.C.M. Hennekam
The amount of credits for a certain Author position, also called write position, does differ by discipline. Some journals publish author names in alphabetical order. This is common practice by publications with many authors.

WoS citations

Time span of publications analysed range from 2000 upto 2015.

8906 (WoS) citations to 277 publications
average 32.15 citations per publication
median: 12
max: 404

This functionality is in Alpha phase.

The data shown here are based on the publications of the UvA-CRIS (May 2016) and the citations found in WoS. The citations to articles are ranked by number of citations. Zero times cited publications are not shown in the diagram. Updated September 5th 2016