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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Prenatal and early postnatal treatment in 3-phosphoglycerate-dehydrogenase deficiency 2004 ·The Lancet ·T. de Koning, (unknown), (unknown), F. A. Beemer, L. Dorland, (unknown), Ruud Berger	87
2	Pediatric Generalized Joint Hypermobility With and Without Musculoskeletal Complaints: A Localized or Systemic Disorder? 2003 ·PEDIATRICS ·Raoul Engelbert, Ruud A. Bank, Ralph J. B. Sakkers, P. J. M. Helders, F. A. Beemer, Cuno S.P.M. Uiterwaal	80
3	Community Genetics in the Netherlands: past and future 2002 ·European Journal of Human Genetics ·(unknown), Lidewij Henneman, (unknown), F. A. Beemer, (unknown), (unknown), (unknown)	1
4	Restrictive dermopathy and fetal behaviour 2001 ·Prenatal Diagnosis ·E Mulder, F. A. Beemer, (unknown)	7
5	Wolf-Hirschhorn (4P-) syndrome in adults. 2001 ·PubMed ·Carlo Marcelis, C. T. R. M. Schrander‐Stumpel, (unknown), (unknown), A.H. Willemse, F. A. Beemer, Sabine Sigaudy, Chantal Missirian, N. Philip, Jean‐Pierre Fryns	9
6	Similarities and differences in the phenotype, genotype and pathogenesis of different spinocerebellar ataxias 2000 ·European Journal of Neurology ·Helenius J. Schelhaas, P.F. Ippel, F. A. Beemer, Gregory S. Hageman	19
7	First trimester nuchal anomalies as a prenatal sign of Zellweger syndrome 2000 ·Prenatal Diagnosis ·G. C. M. L. Christiaens, Jennie M. Pater, (unknown), (unknown), R. J. A. Wanders, F. A. Beemer	8
8	Glycogen Storage Disease Type II: Birth Prevalence Agrees with Predicted Genotype Frequency 1999 ·Public Health Genomics ·Margreet G.E.M. Ausems, (unknown), (unknown), O. P. van Diggelen, Ron A. Wevers, Ben J. H. M. Poorthuis, Klary E. Niezen‐Koning, Ans T. van der Ploeg, F. A. Beemer, Arnold Reuser, L. Sandkuijl, John H. J. Wokke	54
9	Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling 1999 ·European Journal of Human Genetics ·M.G.E.M. Ausems, (unknown), (unknown), (unknown), F. A. Beemer, J.H.J. Wokke, L. Sandkuijl, A. J. J. Reuser, A. van der Ploeg	229
10	A complex haemoglobinopathy diagnosis in a family with both βo- and αo/+-thalassaemia homozygosity 1999 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Peter van Delft, (unknown), F. A. Beemer, (unknown)	14
11	Clinical, pathological and molecular genetic findings in a case of neonatal Marfan syndrome 1999 ·Acta Paediatrica ·Dorine Bresters, (unknown), (unknown), (unknown), Gerard Pals, F. A. Beemer	19
12	Unusual association of congenital malformations 1998 ·Clinical Dysmorphology ·Bernadette P. M. van Nesselrooij, Wim G.M. Spliet, F. A. Beemer	3
13	Prenatal diagnosis of Niemann-Pick disease type C 1992 ·Clinica Chimica Acta ·(unknown), H.C. Janse, O. P. van Diggelen, Frans J. Los, F. A. Beemer, Wim J. Kleijer	11
14	Salla disease variant in a Dutch patient 1992 ·European Journal of Pediatrics ·Grazia M.S. Mancini, (unknown), F.W. Verheijen, O. P. van Diggelen, H.C. Janse, Wim J. Kleijer, F. A. Beemer, F.G.I. Jennekens	20
15	[Molecular genetic aspects of phenylketonuria (PKU)]. 1991 ·PubMed ·Jacques C. Giltay, (unknown), Roel de Weger, M. Durán, R. Berger, F. A. Beemer	1
16	Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis 1988 ·European Journal of Pediatrics ·Jaak Jaeken, S. K. Wadman, M. Durán, (unknown), F. A. Beemer, (unknown), (unknown), Peter de Cock, Françoise Van den Bergh, Marie Vincent, Greet Van den Berghe	103
17	Gingival fibrinoid deposits in Ehlers‐Danlos syndrome 1987 ·Journal of Oral Pathology and Medicine ·Piet J. Slootweg, F. A. Beemer	13
18	Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21 → q25) and del(1)(q41 → q43) 1985 ·Clinical Genetics ·F. A. Beemer, (unknown), (unknown), Bert Janssen	14
19	Failure to detect fetal obstructive uropathy by second trimester ultrasound 1985 ·Prenatal Diagnosis ·J. W. Wladimiroff, F. A. Beemer, (unknown), Patricia A. Stewart, (unknown), Eric D. Wolff	6
20	Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome 1985 ·Clinical Genetics ·H. F. de France, F. A. Beemer, (unknown), (unknown)	14

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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