P H Reitsma

1.2k citations

20 papers · 878 indexed · h-index 10

Hematology top 1%
Internal Medicine top 1%
Genetics top 5%
Cardiology and Cardiovascular Medicine top 10%
Molecular Biology

Co-authors: R M Bertina S R Poort J A Conkie Isobel D. Walker Robert C. Tait S I A M Islam Frances McCall Frances M. Sladek
Topics: Blood Coagulation and Thrombosis Mechanisms (11 papers)Hemophilia Treatment and Research (11 papers)Platelet Disorders and Treatments (5 papers)
Cited by: Internal Medicine Hematology Genetics
Journals: Proceedings of the National Academy of Sciences Nucleic Acids Research FEBS Letters
Partner nations: Netherlands United Kingdom Germany

In The Last Decade

P H Reitsma

20 papers receiving 852 citations

Peers

Replace C Rothschild with:

C Rothschild France

Salvador Grancha Spain

Raúl Teruel‐Montoya Spain

Anne M. Sproul United Kingdom

Elsy Sjörin Sweden

Winifred Trotman United States

Andrew C. Parker United States

Michio Sakai Japan

Giovanna Borrelli Italy

Malcolm A. Cunningham Australia

P H Reitsma relative to C Rothschild France C Rothschild's profile →

Citations per field

00.5×2×4×6×7.5×

C Rothschild · 1×

×0.8 740/983

HEMAT

×7.5 301/40

IM

×1.0 193/193

GENET

×2.2 155/71

CCM

×0.9 143/167

MB

Citations per year

2016

2017

2018

2019

2020

2021

2022

2023

2024

2025

Countries citing papers authored by P H Reitsma

Since Specialization

Citations

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

Fields of papers citing papers by P H Reitsma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P H Reitsma. 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 P H Reitsma. The network helps show where P H Reitsma may publish in the future.

Co-authorship network of co-authors of P H Reitsma

This figure shows the co-authorship network connecting the top 25 collaborators of P H Reitsma. A scholar is included among the top collaborators of P H Reitsma 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 P H Reitsma. P H Reitsma 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

#	Work	Indexed citations
1	Biogenesis of Weibel-Palade bodies in von Willebrand's disease variants with impaired von Willebrand factor intrachain or interchain disulfide bond formation 2011 ·Haematologica ·Jiong‐Wei Wang,Dafna J. Groeneveld,(unknown),Richard Dirven,Karine M. Valentijn,Jan Voorberg,P H Reitsma,Jeroen Eikenboom	28
2	Novel human pathological mutations. Gene symbol: COL7A1. Disease: Epidermolysis Bullosa, Distrophic. 2009 ·PubMed ·(unknown),(unknown),Delphine Borgel,Martine Alhenc‐Gelas,C. Arnold Spek,(unknown),Sophie Gandrille,P H Reitsma,(unknown)	3
3	Factor XIII Val34Leu Is a Genetic Factor Involved in the Aetiology of Venous Thrombosis 1999 ·Thrombosis and Haemostasis ·P H Reitsma,Dayse Maria Lourenço,Francisco Humberto de Abreu Maffei,Vânia M. Morelli,(unknown),Astolfo Gomes de Mello Araújo,Carlos Eli Piccinato,Marco A. Zago,(unknown)	107
4	The usefulness of single-strand DNA conformation polymorphism analysis to detect mutations in protein C deficiency 1997 ·Blood Coagulation & Fibrinolysis ·(unknown),S R Poort,Rogier M. Bertina,P H Reitsma	1
5	Protein C deficiency: summary of the 1995 database update 1996 ·Nucleic Acids Research ·P H Reitsma	30
6	The inheritance and molecular genetics of von Willebrand's disease 1995 ·Haemophilia ·Jeroen Eikenboom,P H Reitsma,(unknown)	5
7	Rapid identification of gene defects in protein C deficiency by temperature gradient gel electrophoresis 1995 ·Blood Coagulation & Fibrinolysis ·Alejandro Hernández,Markus Uhrberg,(unknown),I. Witt,P H Reitsma,Peter Wernet	4
8	Prevalence of Protein C Deficiency in the Healthy Population 1995 ·Thrombosis and Haemostasis ·Robert C. Tait,Isobel D. Walker,P H Reitsma,S I A M Islam,Frances McCall,S R Poort,J A Conkie,R M Bertina	241
9	Identification of Eight Point Mutations in Protein S Deficiency Type I – Analysis of 15 Pedigrees 1995 ·Thrombosis and Haemostasis ·P H Reitsma,E. Gómez,S R Poort,R M Bertina	28
10	Protein C Deficiency: A Database of Mutations, 1995 Update 1995 ·Thrombosis and Haemostasis ·P H Reitsma,Francesca Bernardi,Rowan G. Doig,Sophie Gandrille,J S Greengard,H Ireland,(unknown),Bent Lind,George L. Long,S R Poort,Hidehiko Saito,Núria Sala,I. Witt,D.N. Cooper	201
11	Haemophilia B: database of point mutations and short additions and deletions, fifth edition, 1994 1994 ·Nucleic Acids Research ·F. Giannelli,(unknown),Steve S. Sommer,D Lillicrap,(unknown),(unknown),P H Reitsma,(unknown),(unknown),G. G. Brownlee	38
12	Seeming homozygosity in type-IIB von Willebrand's disease due to a polymorphism within the sequence of a commonly used primer 1994 ·Annals of Hematology ·Jeroen Eikenboom,P H Reitsma,E Briët	4
13	Haemophilia B Leyden: the effect of mutations at position +13 on the liver-specific transcription of the factor IX gene. 1994 ·PubMed ·(unknown),(unknown),R M Bertina,P H Reitsma	6
14	Haemophilia B: database of point mutations and short additions and deletions—fourth edition, 1993 1993 ·Nucleic Acids Research ·F. Giannelli,(unknown),Katherine A. High,(unknown),M.‐C. Poon,Megan Ludwig,R. Schwaab,P H Reitsma,(unknown),(unknown),G. G. Brownlee	35
15	Twelve novel and two recurrent mutations in 14 Austrian families with hereditary protein C deficiency 1993 ·Blood Coagulation & Fibrinolysis ·S R Poort,Ingrid Pabinger-Fasching,Christine Mannhalter,P H Reitsma,R M Bertina	26
16	Double Strand Conformation Polymorphism (DSCP) Detects Two Point Mutations at Codon 280 (AAC→ATC) and at Codon 431 (TAC→AAC) of the Blood Coagulation Factor VIII Gene 1993 ·Thrombosis and Haemostasis ·(unknown),P H Reitsma,E Briët	8
17	Disruption of a binding site for hepatocyte nuclear factor 4 results in hemophilia B Leyden. 1992 ·Proceedings of the National Academy of Sciences ·(unknown),Frances M. Sladek,R M Bertina,P H Reitsma	93
18	Localization of transcription initiation sites in the human coagulation factor IX gene 1990 ·FEBS Letters ·(unknown),Rogier M. Bertina,P H Reitsma	5
19	Application of Two Neutral Mspl DNA Polymorphisms in the Analysis of Hereditary Protein C Deficiency 1990 ·Thrombosis and Haemostasis ·P H Reitsma,(unknown),(unknown),Pieter A. van der Velden,C.F. Allaart,(unknown),S R Poort,R M Bertina	8
20	A Dutch family with moderately severe hemophilia B (Factor IX_Heerde) has a missense mutation identical to that of factor lX_{London 2} 1989 ·Nucleic Acids Research ·S R Poort,E Briët,R M Bertina,P H Reitsma	7

About P H Reitsma

P H Reitsma is a scholar working on Hematology, Genetics and Internal Medicine, having authored 20 papers that have together received 878 indexed citations. Recurring topics across this work include Blood Coagulation and Thrombosis Mechanisms (11 papers), Hemophilia Treatment and Research (11 papers) and Platelet Disorders and Treatments (5 papers). The work is most often cited by research in Internal Medicine (301 citations), Hematology (740 citations) and Genetics (193 citations). P H Reitsma has collaborated with scholars based in Netherlands, United Kingdom and Germany. Frequent co-authors include R M Bertina, S R Poort, J A Conkie, Isobel D. Walker, Robert C. Tait, S I A M Islam, Frances McCall, Frances M. Sladek, I. Witt and Sophie Gandrille. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and FEBS Letters.

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