F. A. Beemer

964 citations

21 papers · 714 indexed · h-index 12

Rheumatology top 5%
- Glycogen Storage Diseases and Myoclonus 2
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 2
Physiology top 10%
- Lysosomal Storage Disorders Research 3
Biochemistry top 10%
Genetics
- Connective tissue disorders research 3
- Genomic variations and chromosomal abnormalities 3
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 3
- Neonatal Health and Biochemistry 2
Cell Biology
- Microtubule and mitosis dynamics 2

Co-authors: 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
Cited by: Rheumatology Clinical Biochemistry Physiology
Journals: The Lancet (1 paper)PEDIATRICS (1 paper)Clinica Chimica Acta (1 paper)
Partner nations: Netherlands Mexico Belgium

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

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

All Works

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20 of 20 papers shown

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

About F. A. Beemer

F. A. Beemer is a scholar working on Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Genetics, having authored 21 papers that have together received 714 indexed citations. Recurring topics across this work include Connective tissue disorders research (3 papers), Prenatal Screening and Diagnostics (3 papers), Lysosomal Storage Disorders Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Neonatal Health and Biochemistry (2 papers), Metabolism and Genetic Disorders (2 papers) and Microtubule and mitosis dynamics (2 papers). The work is most often cited by research in Rheumatology (248 citations), Clinical Biochemistry (106 citations) and Physiology (293 citations). F. A. Beemer has collaborated with scholars based in Netherlands, Mexico and Belgium. Frequent 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. Their work appears in journals such as The Lancet, PEDIATRICS and Clinica Chimica Acta.

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