Fred Petrij

760 total citations
18 papers, 412 citations indexed

About

Fred Petrij is a scholar working on Developmental Biology, Molecular Biology and Surgery. According to data from OpenAlex, Fred Petrij has authored 18 papers receiving a total of 412 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Developmental Biology, 7 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Fred Petrij's work include Congenital limb and hand anomalies (8 papers), Genomics and Chromatin Dynamics (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Fred Petrij is often cited by papers focused on Congenital limb and hand anomalies (8 papers), Genomics and Chromatin Dynamics (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Fred Petrij collaborates with scholars based in Netherlands, United States and Australia. Fred Petrij's co-authors include Rachel H. Giles, Hans G. Dauwerse, Martijn H. Breuning, Dorien J.M. Peters, Ruthann I. Blough, Jack H. Rubinstein, Lester Weiss, Johannes G. Dauwerse, Howard M. Saal and Tamara Lushnikova and has published in prestigious journals such as Blood, Biochemical and Biophysical Research Communications and Thrombosis and Haemostasis.

In The Last Decade

Fred Petrij

18 papers receiving 399 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fred Petrij Netherlands	11	228	153	135	101	67	18	412
Isabelle Gicquel France	13	312 1.4×	29 0.2×	236 1.7×	26 0.3×	62 0.9×	21	453
Farooq Ahmad Pakistan	12	272 1.2×	108 0.7×	227 1.7×	25 0.2×	3 0.0×	38	421
Maria Luigia Cavaliere Italy	13	257 1.1×	21 0.1×	171 1.3×	34 0.3×	4 0.1×	19	372
Satoshi Ishikiriyama Japan	10	289 1.3×	26 0.2×	283 2.1×	20 0.2×	7 0.1×	21	472
Q. Tian Wang United States	10	427 1.9×	15 0.1×	134 1.0×	19 0.2×	15 0.2×	13	484
Sylvie Odent France	9	298 1.3×	29 0.2×	276 2.0×	55 0.5×	5 0.1×	15	512
A Baxová Czechia	10	243 1.1×	21 0.1×	246 1.8×	39 0.4×	3 0.0×	40	416
Josephine Wincent Sweden	12	243 1.1×	16 0.1×	214 1.6×	51 0.5×	5 0.1×	19	467
Hugo Vega Colombia	6	477 2.1×	19 0.1×	149 1.1×	10 0.1×	11 0.2×	10	583
Andreas Hehr Germany	6	490 2.1×	36 0.2×	568 4.2×	56 0.6×	6 0.1×	12	747

Countries citing papers authored by Fred Petrij

Since Specialization

Citations

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

Fields of papers citing papers by Fred Petrij

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fred Petrij. 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 Fred Petrij. The network helps show where Fred Petrij may publish in the future.

Co-authorship network of co-authors of Fred Petrij

This figure shows the co-authorship network connecting the top 25 collaborators of Fred Petrij. A scholar is included among the top collaborators of Fred Petrij 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 Fred Petrij. Fred Petrij 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:

18 of 18 papers shown

Rijneveld, Anita W., et al.. (2015). Value-Based Health Care (VBHC) in Sickle Cell Disease: A Dutch Initiative. Blood. 126(23). 5572–5572. 2 indexed citations

Huang, Lan, et al.. (2014). Nephrocalcinosis as adult presentation of Bartter syndrome type II.. PubMed. 72(2). 91–3. 22 indexed citations

Sanders, Yvonne, Fred Petrij, Marjon H. Cnossen, et al.. (2013). Response to desmopressin is strongly dependent on F8 gene mutation type in mild and moderate haemophilia A. Thrombosis and Haemostasis. 109(3). 440–449. 22 indexed citations

Krapels, Ingrid P.C., Renate C. Zekveld-Vroon, Jan C. Oosterwijk, et al.. (2013). After the Introduction into the National Newborn Screening Program: Who Is Receiving Genetic Counseling for Hemoglobinopathies in The Netherlands?. Public Health Genomics. 17(1). 16–22. 6 indexed citations

Sanders, Yvonne, et al.. (2011). Relation Between Mutations in FVIII Gene and Response to Desmopressin in Patients with Hemophilia A. Blood. 118(21). 29–29. 1 indexed citations

Wagner, Anja, et al.. (2007). FAP: Challenges in Testing Children. Nursing and Health Sciences. 9(3). 237–237. 1 indexed citations

Petrij, Fred, et al.. (2006). Recessive yellow in the Mongolian gerbil (Meriones unguiculatus). Data Archiving and Networked Services (DANS). 43(4). 319–327. 1 indexed citations

Petrij, Fred. (2001). A Second Acromelanistic Allelomorph at the Albino Locus of the Mongolian Gerbil (Meriones unguiculatus). Journal of Heredity. 92(1). 74–78. 10 indexed citations

Blough, Ruthann I., Fred Petrij, Johannes G. Dauwerse, et al.. (2000). Variation in microdeletions of the cyclic AMP-responsive element-binding protein gene at chromosome band 16p13.3 in the Rubinstein-Taybi syndrome. American Journal of Medical Genetics. 90(1). 29–34. 42 indexed citations

10.

Petrij, Fred, et al.. (2000). Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations. Journal of Medical Genetics. 37(3). 168–176. 81 indexed citations

11.

Petrij, Fred, Josephine C. Dorsman, Hans G. Dauwerse, et al.. (2000). Rubinstein-Taybi syndrome caused by a de novo reciprocal translocation t(2;16)(q36.3;p13.3). American Journal of Medical Genetics. 92(1). 47–52. 28 indexed citations

12.

Taine, Laurence, Cyril Goizet, Fred Petrij, et al.. (1998). Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein‐Taybi syndrome. American Journal of Medical Genetics. 78(3). 267–270. 3 indexed citations

13.

Taine, Laurence, Cyril Goizet, Fred Petrij, et al.. (1998). Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein-Taybi syndrome. American Journal of Medical Genetics. 78(3). 267–270. 20 indexed citations

14.

Giles, Rachel H., Fred Petrij, Hans G. Dauwerse, et al.. (1997). Construction of a 1.2-Mb Contig Surrounding, and Molecular Analysis of, the Human CREB-Binding Protein (CBP/CREBBP) Gene on Chromosome 16p13.3. Genomics. 42(1). 96–114. 56 indexed citations

15.

Giles, Rachel H., Fred Petrij, J. Wessels, et al.. (1997). Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16). Leukemia. 11(12). 2087–2096. 55 indexed citations

16.

McGaughran, Julie, Lorraine Gaunt, J. F. Doré, et al.. (1996). Rubinstein-Taybi syndrome with deletions of FISH probe RT1 at 16p13.3: two UK patients.. Journal of Medical Genetics. 33(1). 82–83. 12 indexed citations

17.

Masuno, Mitsuo, et al.. (1994). Submicroscopic deletion of chromosome region 16p13.3 in a Japanese patient with Rubinstein‐Taybi syndrome. American Journal of Medical Genetics. 53(4). 352–354. 18 indexed citations

18.

Petrij, Fred, et al.. (1993). The Mouse Low-Density Lipoprotein Receptor Gene: cDNA Sequence and Exon-Intron Structure. Biochemical and Biophysical Research Communications. 191(3). 880–886. 32 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.

Explore authors with similar magnitude of impact