Peter van Delft

737 citations

40 papers · 608 · h-index 14

Impact in

Genetics top 2%
- Hemoglobinopathies and Related Disorders
- Genomics and Rare Diseases
Hematology top 2%
- Iron Metabolism and Disorders
- Blood groups and transfusion

Papers in

Genetics 37
- Hemoglobinopathies and Related Disorders 37
Hematology 25
- Iron Metabolism and Disorders 24
- Blood groups and transfusion 6

Co-authors: Cornelis L. Harteveld (36 shared papers)Paola Giordano (10 shared papers)Piero C. Giordano (29 shared papers)Luigi F. Bernini (8 shared papers)Majid Yavarian (1 shared paper)Esther D. Quakkelaar (1 shared paper)Marelle J. Bouva (3 shared papers)F. G. A. Versteegh (5 shared papers)
Journals: British Journal of Haematology (5 papers)Hemoglobin (26 papers)European Journal Of Haematology (2 papers)European Journal of Human Genetics (1 paper)American Journal of Hematology (1 paper)
Partner nations: Netherlands France Tunisia

In The Last Decade

Peter van Delft

40 papers receiving 600 citations

Peers

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-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi‐ethnic populations International Journal of Laboratory Hematology ·Peter van Delft, Egbert Lenters, Margreet Bakker‐Verweij, Michael de Korte, U. BAYLAN, Cornelis L. Harteveld, Paola Giordano	2009	111
2	Molecular spectrum of α‐thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects American Journal of Hematology ·Cornelis L. Harteveld, Majid Yavarian, Amine Zoraï, Esther D. Quakkelaar, Peter van Delft, Paola Giordano	2003	70
3	Known and new delta globin gene mutations and their diagnostic significance. PubMed ·Marelle J. Bouva, Cornelis L. Harteveld, Peter van Delft, Piero C. Giordano	2006	38
4	MOLECULAR SPECTRUM OFα-THALASSEMIA IN TUNISIA: EPIDEMIOLOGY AND DETECTION AT BIRTH Hemoglobin ·Amine Zoraï, Cornelis L. Harteveld, Achech Bakir, Peter van Delft, A. Falfoul, Koussay Dellagi, Salem Abbès, Piero C. Giordano	2002	31
5	Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method Clinical & Laboratory Haematology ·Paola Giordano, Peter van Delft, D. Batelaan, C. L. Harteveld, Luigi F. Bernini	1999	30
6	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 ·Cornelis L. Harteveld, J. G. A. M. Heister, Paola Giordano, D. Batelaan, Peter van Delft, H. L. Haak, P. Wijermans, Monique Losekoot, Luigi F. Bernini	1996	23
7	Hb GROENE HART: A NEW Pro→Ser AMINO ACID SUBSTITUTION AT POSITION 119 OF THEα1-GLOBIN CHAIN IS ASSOCIATED WITH A MILDα-THALASSEMIA PHENOTYPE Hemoglobin ·Cornelis L. Harteveld, Peter van Delft, Rob Plug, F. G. A. Versteegh, Balt Hagen, Irene van Rooijen, Peter J.M.J. Kok, Henri Wajcman, J. Kister, Piero C. Giordano	2002	23
8	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 ·Piero C. Giordano, Sonja Zweegman, Nicole Akkermans, Sandra G.J. Arkesteijn, Peter van Delft, F. G. A. Versteegh, Henri Wajcman, Cornelis L. Harteveld	2007	21
9	Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype Hemoglobin ·Cornelis L. Harteveld, F. G. A. Versteegh, Peter J.M.J. Kok, Irene H. van Rooijen-Nijdam, Peter van Delft, Piero C. Giordano	2006	20
10	Phenotype variability of the dominant β-thalassemia induced in four Dutch families by the rare cd121 (G→T) mutation Annals of Hematology ·Paola Giordano, Cornelis L. Harteveld, J. J. Michiels, W. J. Terpstra, Lodewijk J. D. M. Schelfhout, Inge M. Appel, D. Batelaan, Peter van Delft, Robert J. Plug, Luigi F. Bernini	1998	19
11	α‐Thalassaemia as a result of a novel splice donor site mutation of the α₁‐globin gene British Journal of Haematology ·Cornelis L. Harteveld, C. Beijer, Peter van Delft, Roberta Zanardini, Luigi F. Bernini, Paola Giordano	2000	19
12	Hb Lepore-Leiden: A New δ/β Rearrangement Associated with a β-Thalassemia Minor Phenotype Hemoglobin ·Cornelis L. Harteveld, Pierre W. Wijermans, Sandra G.J. Arkesteijn, Peter van Delft, Jean‐Louis Kerkhoffs, Piero C. Giordano	2008	17
13	Hb Utrecht [α₂ 129(H12)Leu → Pro], a new unstable α2‐chain variant associated with a mild α‐thalassaemic phenotype British Journal of Haematology ·Cornelis L. Harteveld, Paola Giordano, Monique Losekoot, J. G. A. M. Heister, D. Batelaan, Peter van Delft, Marrie C.A. Bruin, Luigi F. Bernini	1996	16
14	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
15	Atypical HbH disease in a Surinamese patient resulting from a combination of the −SEA and −α^3.7 deletions with HbC heterozygosity British Journal of Haematology ·Paola Giordano, C. L. Harteveld, J. J. Michiels, W. J. Terpstra, D. Batelaan, Peter van Delft, Robert J. Plug, M. J. R. VAN DER WIELEN, Monique Losekoot, Luigi F. Bernini	1997	13
16	An α‐Thalassemia Phenotype in a Dutch Hindustani, Caused by a New Point Mutation that Creates an Alternative Splice Donor Site in the First Exon of the α2‐Globin Gene Hemoglobin ·Cornelis L. Harteveld, Pierre W. Wijermans, Peter van Delft, Ellen Rasp, Hans L. Haak, Piero C. Giordano	2004	12
17	Hb Oegstgeest [α104(G11)Cys → Ser (α1)]. A New Hemoglobin Variant Associated with a Mild α-Thalassemia Phenotype Hemoglobin ·Cornelis L. Harteveld, Lieke Rozendaal, Nico A. Blom, Shirley Lo-A-Njoe, Nicole Akkerman, Sandra Arkestijn, Peter van Delft, Piero C. Giordano	2005	12
18	Hb Amsterdam [α32(B13)Met→Ile (α2)]: A New Unstable Variant Associated with an α-Thalassemia Phenotype and a New African Polymorphism Hemoglobin ·Cornelis L. Harteveld, Marc Vervloet, Sonja Zweegman, Peter van Delft, Nicole Akkermans, Sandra Arkestijn, Piero C. Giordano	2005	10
19	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 ·Cornelis L. Harteveld, Pierre W. Wijermans, Juliette E. L. M. de Ree, Pauline Ter Hal, Peter van Delft, Irene H. van Rooijen-Nijdam, Ellen Rasp, Peter J.M.J. Kok, John H. M. Souverijn, F. G. A. Versteegh, Piero C. Giordano	2004	10
20	α‐thalassaemia masked by β gene defects and a new polyadenylation site mutation on the α2‐globin gene European Journal Of Haematology ·Cornelis L. Harteveld, Wytze P. Oosterhuis, Christian H.H. Schoenmakers, Hardjawardhama Ananta, Snježana Kos, Margaretha Bakker Verweij, Peter van Delft, Sandra G.J. Arkesteijn, Marion Phylipsen, Piero C. Giordano	2009	9

About Peter van Delft

Peter van Delft is a scholar working on Genetics, Hematology, Physiology, Cell Biology and Molecular Biology, having authored 40 papers that have together received 608 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (37 papers), Iron Metabolism and Disorders (24 papers), Erythrocyte Function and Pathophysiology (12 papers), Blood groups and transfusion (6 papers), Hemoglobin structure and function (6 papers), Machine Learning in Bioinformatics (2 papers), Pancreatic function and diabetes (2 papers) and RNA and protein synthesis mechanisms (2 papers). The work is most often cited by research in Genetics (561 citations), Hematology (447 citations), Pediatrics, Perinatology and Child Health (111 citations), Physiology (112 citations) and Cell Biology (44 citations). Peter van Delft has collaborated with scholars based in Netherlands, France and Tunisia. Frequent co-authors include Cornelis L. Harteveld, Paola Giordano, Piero C. Giordano, Luigi F. Bernini, Majid Yavarian, Esther D. Quakkelaar, Marelle J. Bouva, F. G. A. Versteegh, Monique Losekoot and Pierre W. Wijermans. Their work appears in journals such as British Journal of Haematology, Hemoglobin, European Journal Of Haematology, European Journal of Human Genetics and American Journal of Hematology.

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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