B. G. A. ter Haar

531 citations

20 papers · 423 indexed · h-index 15

Developmental Biology top 10%
- Congenital limb and hand anomalies 2
Genetics
- Genomic variations and chromosomal abnormalities 4
Nephrology
Cancer Research
- Carcinogens and Genotoxicity Assessment 2
Genetics
- Genomic variations and chromosomal abnormalities 4
Molecular Biology
- DNA Repair Mechanisms 3
- Molecular Biology Techniques and Applications 3
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 3
- Fetal and Pediatric Neurological Disorders 2
Plant Science
- Chromosomal and Genetic Variations 2

Co-authors: T. W. J. Hustinx J. M. J. C. Scheres Corry M.R. Weemaes F.J.M. Gabreëls W.O. Renier Renate Burgemeister T. L. Oei C. H. M. M. de Bruyn
Cited by: Developmental Biology Genetics Nephrology
Journals: Acta Neuropathologica (1 paper)Journal of Medical Genetics (1 paper)Human Genetics (3 papers)
Partner nations: Netherlands Germany United States

In The Last Decade

B. G. A. ter Haar

20 papers receiving 388 citations

Peers

Countries citing papers authored by B. G. A. ter Haar

Since Specialization

Citations

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

Fields of papers citing papers by B. G. A. ter Haar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by B. G. A. ter Haar. 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 B. G. A. ter Haar. The network helps show where B. G. A. ter Haar may publish in the future.

Co-authorship network

The 25 scholars most cited alongside B. G. A. ter Haar, 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 B. G. A. ter Haar Line = papers co-authored together B. G. A. ter Haar links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Regional heterogeneity of EGFR gene amplification and nuclear morphology in glioblastomas. An investigation using laser microdissection and pressure catapulting. PubMed ·Reinhold Nafe,Wolfgang Glienke,Renate Burgemeister,Rainer Gangnus,B. G. A. ter Haar,Antje Pries,W. Schlote	2004	7
2	Laser Microdissection and Pressure Catapulting (LMPC) in Paraffin Sections Mounted on Glass Slides. A Methodological Report Pathology - Research and Practice ·Reinhold Nafe,Rainer Gangnus,Wolfgang Glienke,Renate Burgemeister,B. G. A. ter Haar,Antje Pries,W. Schlote	2003	3
3	High Quality RNA Retrieved from Samples Obtained by Using LMPC (Laser Microdissection and Pressure Catapulting) Technology Pathology - Research and Practice ·Renate Burgemeister,Rainer Gangnus,B. G. A. ter Haar,Karin Schütze,Ulrich Sauer	2003	32
4	Orbital cyst in addition to congenital cerebral and focal dermal malformations: a new entity Clinical Genetics ·J.W. Delleman,J. W. E. Oorthuys,E. M. Bleeker‐Wagemakers,B. G. A. ter Haar,J. W. Ferguson	1984	33
5	Progressive Idiopathic Strio-Pallido-Dentate Calcinosis (Fahr’s Disease) with Autosomal Recessive Inheritance European Neurology ·Minke Smits,F.J.M. Gabreëls,H.O.M. Thijssen,Ryan Lam,S. L. H. Notermans,B. G. A. ter Haar,J J G Prick	1983	36
6	Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibs Clinical Genetics ·W.O. Renier,F. A. E. Nabben,T. W. J. Hustinx,J.H. Veerkamp,B.J. Otten,H. J. ter Laak,B. G. A. ter Haar,F.J.M. Gabreëls	1983	37
7	Autosomal dominant idiopathic hypoparathyroidism and nervous system dysfunction: report of three cases and review of the literature Journal of Neurology ·Minke Smits,F. Gabreëls,P. Froeling,H.O.M. Thijssen,E. J. Colon,B. G. A. ter Haar,C. Ruland,Renita Lam	1982	21
8	X-Linked congenital hydrocephalus Clinical Neurology and Neurosurgery ·W.O. Renier,B. G. A. ter Haar,J.L. Slooff,T. W. J. Hustinx,F.J.M. Gabreëls	1982	16
9	Connatal Pelizaeus-Merzbacher Disease with congenital stridor in two maternal cousins Acta Neuropathologica ·W.O. Renier,F.J.M. Gabreëls,T. W. J. Hustinx,H. H. J. Jaspar,J.A.G. Geelen,U.J.G. van Haelst,E. J. P. Lommen,B. G. A. ter Haar	1981	23
10	Epidemiology of alpha1-antitrypsin deficiency in the Netherlands Human Genetics ·Joop H. Dijkman,T J Penders,J. A. Kramps,H. J. A. Sonderkamp,W. G. M. van den Broek,B. G. A. ter Haar	1980	14
11	Karyotype instability with multiple 7/14 and 7/7 rearrangements Human Genetics ·T. W. J. Hustinx,J. M. J. C. Scheres,Corry M.R. Weemaes,B. G. A. ter Haar,Annelli Janssen	1979	31
12	Immune responses in four patients with Bloom syndrome Clinical Immunology and Immunopathology ·Corry M.R. Weemaes,J. A. J. M. Bakkeren,B. G. A. ter Haar,T. W. J. Hustinx,P.J.J. Van Munster	1979	28
13	2:2 and 3:1 Meiotic disjunctions in a carrier of a reciprocal 10/14 translocation Clinical Genetics ·J. M. J. C. Scheres,T. W. J. Hustinx,B. G. A. ter Haar,F. J. Rutten,H. H. A. M van der Mee‐Wienen	1978	1
14	Bloom's syndrome in two Dutch families Clinical Genetics ·T. W. J. Hustinx,B. G. A. ter Haar,J. M. J. C. Scheres,F. J. Rutten,(unknown),Rainer L. E. Hoppe,Annelli Janssen	1977	17
15	The Nathalie syndrome. A new hereditary syndrome Clinical Genetics ·Cor W. R. J. Cremers,B. G. A. ter Haar,Th. J. G. van Rens	1975	9
16	Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution. PubMed ·T. W. J. Hustinx,B. G. A. ter Haar,J. M. J. C. Scheres,F. J. Rutten	1974	6
17	Trisomy for the short arm of chromosome No. 10 Clinical Genetics ·T. W. J. Hustinx,B. G. A. ter Haar,J. M. J. C. Scheres,F. J. Rutten	1974	26
18	The Trismus-Pseudocampylodactyly Syndrome Journal of Medical Genetics ·B. G. A. ter Haar,R.F. van Hoof	1974	25
19	A presumptive tetrasomy for the short arm of chromosome 9 Human Genetics ·F. J. Rutten,J. M. J. C. Scheres,T. W. J. Hustinx,B. G. A. ter Haar	1974	33
20	Studies on hair roots for carrier detection in hypoxanthine‐guanine phosphoribosyl transferase deficiency Clinical Genetics ·C. H. M. M. de Bruyn,T. L. Oei,B. G. A. ter Haar	1974	25

About B. G. A. ter Haar

B. G. A. ter Haar is a scholar working on Developmental Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 20 papers that have together received 423 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), DNA Repair Mechanisms (3 papers), Molecular Biology Techniques and Applications (3 papers), Prenatal Screening and Diagnostics (3 papers), Congenital limb and hand anomalies (2 papers), Carcinogens and Genotoxicity Assessment (2 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Developmental Biology (16 citations), Genetics (160 citations) and Nephrology (29 citations). B. G. A. ter Haar has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include T. W. J. Hustinx, J. M. J. C. Scheres, Corry M.R. Weemaes, F.J.M. Gabreëls, W.O. Renier, J. M. J. C. Scheres, Renate Burgemeister, T. L. Oei, C. H. M. M. de Bruyn and H.O.M. Thijssen. Their work appears in journals such as Acta Neuropathologica, Journal of Medical Genetics and Human Genetics.

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.

Explore authors with similar magnitude of impact