F. A. Beemer

964 total citations
21 papers, 714 citations indexed

About

F. A. Beemer is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, F. A. Beemer has authored 21 papers receiving a total of 714 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in F. A. Beemer's work include Connective tissue disorders research (3 papers), Prenatal Screening and Diagnostics (3 papers) and Lysosomal Storage Disorders Research (3 papers). F. A. Beemer is often cited by papers focused on Connective tissue disorders research (3 papers), Prenatal Screening and Diagnostics (3 papers) and Lysosomal Storage Disorders Research (3 papers). F. A. Beemer collaborates with scholars based in Netherlands, Mexico and Belgium. F. A. Beemer's co-authors include L. Sandkuijl, A. J. J. Reuser, M.G.E.M. Ausems, A. van der Ploeg, J.H.J. Wokke, Ralph J. B. Sakkers, Ruud A. Bank, Raoul Engelbert, P. J. M. Helders and Cuno S.P.M. Uiterwaal and has published in prestigious journals such as The Lancet, PEDIATRICS and Clinica Chimica Acta.

In The Last Decade

F. A. Beemer

21 papers receiving 691 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. A. Beemer Netherlands	12	293	248	232	167	106	21	714
C B Whitley United States	17	556 1.9×	209 0.8×	287 1.2×	138 0.8×	122 1.2×	30	970
Shuan-Pei Lin Taiwan	19	371 1.3×	206 0.8×	239 1.0×	158 0.9×	122 1.2×	39	793
Esmée Oussoren Netherlands	15	383 1.3×	166 0.7×	245 1.1×	106 0.6×	89 0.8×	32	768
I Maire France	17	785 2.7×	287 1.2×	341 1.5×	146 0.9×	82 0.8×	85	1.2k
David Kronn United States	15	195 0.7×	274 1.1×	362 1.6×	270 1.6×	147 1.4×	35	1.0k
Shu-Chuan Chiang Taiwan	10	426 1.5×	197 0.8×	208 0.9×	70 0.4×	113 1.1×	20	721
Hélène Ogier France	13	292 1.0×	113 0.5×	443 1.9×	86 0.5×	415 3.9×	16	877
Joyce A. Kobori United States	11	329 1.1×	178 0.7×	277 1.2×	93 0.6×	234 2.2×	14	686
M. F. Niermeijer Netherlands	18	299 1.0×	87 0.4×	300 1.3×	212 1.3×	50 0.5×	44	902
Moeenaldeen AlSayed Saudi Arabia	15	333 1.1×	130 0.5×	254 1.1×	183 1.1×	86 0.8×	49	737

Countries citing papers authored by F. A. Beemer

Since Specialization

Citations

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

Fields of papers citing papers by F. A. Beemer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. A. Beemer. 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 F. A. Beemer. The network helps show where F. A. Beemer may publish in the future.

Co-authorship network of co-authors of F. A. Beemer

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

All Works

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

20 of 20 papers shown

Koning, T. de, et al.. (2004). Prenatal and early postnatal treatment in 3-phosphoglycerate-dehydrogenase deficiency. The Lancet. 364(9452). 2221–2222. 87 indexed citations

Engelbert, Raoul, Ruud A. Bank, Ralph J. B. Sakkers, et al.. (2003). Pediatric Generalized Joint Hypermobility With and Without Musculoskeletal Complaints: A Localized or Systemic Disorder?. PEDIATRICS. 111(3). e248–e254. 80 indexed citations

Henneman, Lidewij, et al.. (2002). Community Genetics in the Netherlands: past and future. European Journal of Human Genetics. 10. 194–194. 1 indexed citations

Mulder, E, et al.. (2001). Restrictive dermopathy and fetal behaviour. Prenatal Diagnosis. 21(7). 581–585. 7 indexed citations

Marcelis, Carlo, C. T. R. M. Schrander‐Stumpel, A.H. Willemse, et al.. (2001). Wolf-Hirschhorn (4P-) syndrome in adults.. PubMed. 12(1). 35–48. 9 indexed citations

Schelhaas, Helenius J., P.F. Ippel, F. A. Beemer, & Gregory S. Hageman. (2000). Similarities and differences in the phenotype, genotype and pathogenesis of different spinocerebellar ataxias. European Journal of Neurology. 7(3). 309–314. 19 indexed citations

Christiaens, G. C. M. L., et al.. (2000). First trimester nuchal anomalies as a prenatal sign of Zellweger syndrome. Prenatal Diagnosis. 20(6). 520–521. 8 indexed citations

Ausems, Margreet G.E.M., O. P. van Diggelen, Ron A. Wevers, et al.. (1999). Glycogen Storage Disease Type II: Birth Prevalence Agrees with Predicted Genotype Frequency. Public Health Genomics. 2(2-3). 91–96. 54 indexed citations

Ausems, M.G.E.M., F. A. Beemer, J.H.J. Wokke, et al.. (1999). Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling. European Journal of Human Genetics. 7(6). 713–716. 229 indexed citations

10.

Delft, Peter van, et al.. (1999). A complex haemoglobinopathy diagnosis in a family with both βo- and αo/+-thalassaemia homozygosity. European Journal of Human Genetics. 7(2). 163–168. 14 indexed citations

11.

Bresters, Dorine, et al.. (1999). Clinical, pathological and molecular genetic findings in a case of neonatal Marfan syndrome. Acta Paediatrica. 88(1). 98–101. 19 indexed citations

12.

Nesselrooij, Bernadette P. M. van, Wim G.M. Spliet, & F. A. Beemer. (1998). Unusual association of congenital malformations. Clinical Dysmorphology. 7(1). 51???54–51???54. 3 indexed citations

13.

Janse, H.C., et al.. (1992). Prenatal diagnosis of Niemann-Pick disease type C. Clinica Chimica Acta. 208(3). 173–181. 11 indexed citations

14.

Mancini, Grazia M.S., F.W. Verheijen, O. P. van Diggelen, et al.. (1992). Salla disease variant in a Dutch patient. European Journal of Pediatrics. 151(8). 590–595. 20 indexed citations

15.

Giltay, Jacques C., et al.. (1991). [Molecular genetic aspects of phenylketonuria (PKU)].. PubMed. 59(3). 77–80. 1 indexed citations

16.

Jaeken, Jaak, S. K. Wadman, M. Durán, et al.. (1988). Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis. European Journal of Pediatrics. 148(2). 126–131. 103 indexed citations

17.

Slootweg, Piet J. & F. A. Beemer. (1987). Gingival fibrinoid deposits in Ehlers‐Danlos syndrome. Journal of Oral Pathology and Medicine. 16(3). 150–152. 13 indexed citations

18.

Beemer, F. A., et al.. (1985). Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21 → q25) and del(1)(q41 → q43). Clinical Genetics. 27(5). 515–519. 14 indexed citations

19.

Wladimiroff, J. W., et al.. (1985). Failure to detect fetal obstructive uropathy by second trimester ultrasound. Prenatal Diagnosis. 5(1). 41–46. 6 indexed citations

20.

France, H. F. de, et al.. (1985). Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome. Clinical Genetics. 27(1). 92–96. 14 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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