Peter van Delft

737 total citations
40 papers, 608 citations indexed

About

Peter van Delft is a scholar working on Genetics, Hematology and Physiology. According to data from OpenAlex, Peter van Delft has authored 40 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Genetics, 25 papers in Hematology and 12 papers in Physiology. Recurrent topics in Peter van Delft's work include Hemoglobinopathies and Related Disorders (37 papers), Iron Metabolism and Disorders (24 papers) and Erythrocyte Function and Pathophysiology (12 papers). Peter van Delft is often cited by papers focused on Hemoglobinopathies and Related Disorders (37 papers), Iron Metabolism and Disorders (24 papers) and Erythrocyte Function and Pathophysiology (12 papers). Peter van Delft collaborates with scholars based in Netherlands, France and United States. Peter van Delft's co-authors include Cornelis L. Harteveld, Paola Giordano, Piero C. Giordano, Luigi F. Bernini, Esther D. Quakkelaar, Majid Yavarian, Marelle J. Bouva, F. G. A. Versteegh, Peter J.M.J. Kok and Pierre W. Wijermans and has published in prestigious journals such as British Journal of Haematology, European Journal of Human Genetics and American Journal of Hematology.

In The Last Decade

Peter van Delft

40 papers receiving 600 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter van Delft Netherlands 14 561 447 112 111 88 40 608
YC Gu United States 6 505 0.9× 387 0.9× 84 0.8× 120 1.1× 96 1.1× 8 546
C Altay United States 12 476 0.8× 375 0.8× 87 0.8× 113 1.0× 121 1.4× 29 561
J. M. Gonzalez‐Redondo United States 13 639 1.1× 479 1.1× 98 0.9× 114 1.0× 131 1.5× 20 702
G. V. Sciarratta Italy 11 292 0.5× 193 0.4× 68 0.6× 88 0.8× 108 1.2× 27 387
A Metaxotou-Mavromati Greece 14 501 0.9× 388 0.9× 68 0.6× 140 1.3× 90 1.0× 28 549
MH Steinberg United States 9 364 0.6× 298 0.7× 49 0.4× 89 0.8× 66 0.8× 10 411
M. B. Coleman United States 10 344 0.6× 258 0.6× 49 0.4× 71 0.6× 62 0.7× 17 377
L. Perseu Italy 12 282 0.5× 207 0.5× 68 0.6× 119 1.1× 56 0.6× 18 334
Konstantinos Varvagiannis Greece 5 309 0.6× 243 0.5× 25 0.2× 96 0.9× 75 0.9× 11 373
PE Nute United States 6 309 0.6× 254 0.6× 146 1.3× 119 1.1× 77 0.9× 8 393

Countries citing papers authored by Peter van Delft

Since Specialization
Citations

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

Fields of papers citing papers by Peter van Delft

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter van Delft. 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 Peter van Delft. The network helps show where Peter van Delft may publish in the future.

Co-authorship network of co-authors of Peter van Delft

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

All Works

20 of 20 papers shown
1.
Phylipsen, Marion, Joanne Traeger‐Synodinos, Peter van Delft, et al.. (2012). A novel α0‐thalassemia deletion in a Greek patient with HbH disease and β‐thalassemia trait. European Journal Of Haematology. 88(4). 356–362. 4 indexed citations
2.
Phylipsen, Marion, et al.. (2010). Hb St. Truiden [α68(E17)Asn→His] and Hb Westeinde [α125(H8)Leu→Gln]: Two New Abnormalities of the α2-Globin Gene. Hemoglobin. 34(5). 439–444. 2 indexed citations
3.
Harteveld, Cornelis L., Peter van Delft, Hans L. Haak, et al.. (2010). Hb Den Haag [β45(CD4)Phe→Tyr]. A New Hemoglobin Variant Observed During Early Pregnancy Diagnostics. Hemoglobin. 34(1). 37–44. 2 indexed citations
4.
Delft, Peter van, et al.. (2009). Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi‐ethnic populations. International Journal of Laboratory Hematology. 31(5). 484–495. 111 indexed citations
5.
Harteveld, Cornelis L., Wytze P. Oosterhuis, Snježana Kos, et al.. (2009). α‐thalassaemia masked by β gene defects and a new polyadenylation site mutation on the α2‐globin gene. European Journal Of Haematology. 84(4). 354–358. 9 indexed citations
6.
Giordano, Piero C., Sonja Zweegman, Peter van Delft, et al.. (2007). The First Case of Hb Groene Hart [α119(H2)Pro→Ser,CCT→TCT (α1)] Homozygosity Confirms That a Thalassemia Phenotype Is Associated with this Abnormal Hemoglobin Variant. Hemoglobin. 31(2). 179–182. 21 indexed citations
7.
Harteveld, Cornelis L., et al.. (2006). α-Thalassemia Phenotype Induced by the New IVS-II-2 (T→A) Splice Donor Site Mutation on the α2-Globin Gene. Hemoglobin. 30(1). 3–7. 6 indexed citations
8.
Harteveld, Cornelis L., et al.. (2006). Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype. Hemoglobin. 30(3). 349–354. 20 indexed citations
9.
10.
Harteveld, Cornelis L., et al.. (2005). Hb Amsterdam [α32(B13)Met→Ile (α2)]: A New Unstable Variant Associated with an α-Thalassemia Phenotype and a New African Polymorphism. Hemoglobin. 29(4). 257–262. 10 indexed citations
11.
Harteveld, Cornelis L., et al.. (2004). Hb Suan‐Dok [α109(G16)Leu→Arg; CTG→CGG (α2)] Described in a Patient of African Ancestry. Hemoglobin. 28(3). 173–176. 5 indexed citations
12.
Harteveld, Cornelis L., Pierre W. Wijermans, Peter van Delft, et al.. (2004). A New Hb Evanston Allele [α14(A12)Trp → Arg] Found Solely, and in the Presence of Common α‐Thalassemia Deletions, in Three Independent Asian Cases. Hemoglobin. 28(1). 1–5. 10 indexed citations
13.
Harteveld, Cornelis L., et al.. (2003). Molecular spectrum of α‐thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects. American Journal of Hematology. 74(2). 99–103. 70 indexed citations
14.
Harteveld, Cornelis L., Peter van Delft, Pierre W. Wijermans, et al.. (2003). A novel 7·9 kb deletion causing α+‐thalassaemia in two independent families of Indian origin. British Journal of Haematology. 120(2). 364–366. 9 indexed citations
15.
Kerkhoffs, Jean‐Louis, Cornelis L. Harteveld, P. Wijermans, et al.. (2000). Very Mild Pathology in a Case of Hb S/β˚-Thalassemia in Combination with a Homozygosity for the α-Thalassemia 3.7 kb Deletion. Hemoglobin. 24(3). 259–263. 4 indexed citations
16.
Berg, H. Marijke van den, Marrie C.A. Bruin, Peter van Delft, et al.. (1999). Hb nijkerk: A new mutation at codons 138/139 of the β-giobin gene inducing severe hemolytic anemia in a dutch girl. Hemoglobin. 23(2). 135–144. 8 indexed citations
17.
Giordano, Paola, Cornelis L. Harteveld, J. J. Michiels, et al.. (1998). Phenotype variability of the dominant β-thalassemia induced in four Dutch families by the rare cd121 (G→T) mutation. Annals of Hematology. 77(6). 249–255. 19 indexed citations
18.
Giordano, Paola, J. J. Michiels, W. J. Terpstra, et al.. (1997). Atypical HbH disease in a Surinamese patient resulting from a combination of the −SEA and −α3.7 deletions with HbC heterozygosity. British Journal of Haematology. 96(4). 801–805. 13 indexed citations
19.
Harteveld, Cornelis L., J. G. A. M. Heister, Paola Giordano, et al.. (1996). An IVS1–116 (A→G) acceptor splice site mutation in the α2 globin gene causing α+ thalassaemia in two Dutch families. British Journal of Haematology. 95(3). 461–466. 23 indexed citations
20.
Harteveld, Cornelis L., Paola Giordano, Monique Losekoot, et al.. (1996). Hb Utrecht [α2 129(H12)Leu → Pro], a new unstable α2‐chain variant associated with a mild α‐thalassaemic phenotype. British Journal of Haematology. 94(3). 483–485. 16 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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