TH Huisman

672 total citations
17 papers, 540 citations indexed

About

TH Huisman is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, TH Huisman has authored 17 papers receiving a total of 540 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Hematology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in TH Huisman's work include Hemoglobinopathies and Related Disorders (13 papers), Iron Metabolism and Disorders (9 papers) and Erythrocyte Function and Pathophysiology (4 papers). TH Huisman is often cited by papers focused on Hemoglobinopathies and Related Disorders (13 papers), Iron Metabolism and Disorders (9 papers) and Erythrocyte Function and Pathophysiology (4 papers). TH Huisman collaborates with scholars based in United States, Switzerland and Netherlands. TH Huisman's co-authors include KD Lanclos, Aleksandar Dimovski, J. G. Gilman, YC Gu, C. Öner, F. Kutlar, J. B. Wilson, Aytemiz Gürgey, Çiğdem Altay and T. A. Stoming and has published in prestigious journals such as Blood, American Journal of Physiology-Legacy Content and Wetlands Ecology and Management.

In The Last Decade

TH Huisman

17 papers receiving 530 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
TH Huisman United States	12	433	301	157	149	84	17	540
J. M. Gonzalez‐Redondo United States	13	639 1.5×	479 1.6×	131 0.8×	114 0.8×	98 1.2×	20	702
YC Gu United States	6	505 1.2×	387 1.3×	96 0.6×	120 0.8×	84 1.0×	8	546
M Patterson Canada	12	359 0.8×	262 0.9×	148 0.9×	90 0.6×	163 1.9×	27	505
John F. Prior Australia	10	347 0.8×	285 0.9×	124 0.8×	124 0.8×	46 0.5×	16	557
P. K. Sukumaran India	13	416 1.0×	289 1.0×	93 0.6×	153 1.0×	64 0.8×	34	525
John G. Gilman United States	11	251 0.6×	151 0.5×	169 1.1×	64 0.4×	109 1.3×	21	464
Nicholas C. Bethlenfalvay United States	10	165 0.4×	91 0.3×	153 1.0×	88 0.6×	90 1.1×	28	451
CD Boehm United States	8	261 0.6×	184 0.6×	139 0.9×	65 0.4×	44 0.5×	10	378
J.M. Kooter Netherlands	5	280 0.6×	143 0.5×	248 1.6×	50 0.3×	31 0.4×	5	445
FF Chehab United States	9	261 0.6×	208 0.7×	97 0.6×	96 0.6×	32 0.4×	10	399

Countries citing papers authored by TH Huisman

Since Specialization

Citations

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

Fields of papers citing papers by TH Huisman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of TH Huisman

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

All Works

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17 of 17 papers shown

Huisman, TH, Frank van Langevelde, & Willem F. de Boer. (2009). Local positive feedback and the persistence and recovery of fringe Avicennia marina (Forssk.) vierh. mangroves. Wetlands Ecology and Management. 17(6). 601–611. 8 indexed citations

Huisman, TH, et al.. (1999). [Characteristics of pedigree cat breeding in the Netherlands: breeds, population increase and litter size].. PubMed. 124(5). 145–8. 3 indexed citations

Dimovski, Aleksandar, et al.. (1994). A novel deletion of approximately 27 kb including the beta-globin gene and the locus control region 3'HS-1 regulatory sequence: beta zero- thalassemia or hereditary persistence of fetal hemoglobin?. Blood. 83(3). 822–827. 21 indexed citations

Öner, C., Aleksandar Dimovski, Çiğdem Altay, et al.. (1992). Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes. Blood. 79(3). 813–819. 87 indexed citations

Plaseska‐Karanfilska, Dijana, et al.. (1991). Hemoglobin Montreal: a new variant with an extended beta chain due to a deletion of Asp, Gly, Leu at positions 73, 74, and 75, and an insertion of Ala, Arg, Cys, Gln at the same location. Blood. 77(1). 178–181. 11 indexed citations

Lanclos, KD, C. Öner, Aleksandar Dimovski, YC Gu, & TH Huisman. (1991). Sequence variations in the 5' flanking and IVS-II regions of the G gamma- and A gamma-globin genes of beta S chromosomes with five different haplotypes. Blood. 77(11). 2488–2496. 87 indexed citations

Öner, R., et al.. (1991). The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C---T mutation at nucleotide-114 of the A gamma-globin gene [letter]. Blood. 77(5). 1124–1125. 22 indexed citations

Zago, M A, et al.. (1990). The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C---- G substitution at nucleotide -195 of the A gamma-globin gene. Blood. 76(9). 1896–1897. 29 indexed citations

Stoming, T. A., et al.. (1989). An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene. Blood. 73(1). 329–333. 41 indexed citations

10.

Han, IS, et al.. (1989). Identical nucleotide sequences of the 3'A gamma globin gene enhancer elements from four different chromosomes. Blood. 73(3). 845–848. 2 indexed citations

11.

Mishima, N., et al.. (1988). Upstream promoter mutation associated with a modest elevation of fetal hemoglobin expression in human adults. Blood. 72(1). 78–81. 1 indexed citations

12.

Beris, P, JC Diaz-Chico, IS Han, et al.. (1988). Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114. Blood. 72(2). 801–805. 48 indexed citations

13.

Mishima, N., et al.. (1988). Upstream promoter mutation associated with a modest elevation of fetal hemoglobin expression in human adults. Blood. 72(1). 78–81. 40 indexed citations

14.

Gilman, J. G. & TH Huisman. (1984). Two independent genetic factors in the beta-globin gene cluster are associated with high G gamma-levels in the HbF of SS patients. Blood. 64(2). 452–457. 61 indexed citations

15.

Wilson, J. B., et al.. (1976). Hb Leslie, an unstable hemoglobin due to deletion of glutaminyl residue beta 131 (H9) occurring in association with beta0-thalassemia, HbC, and HbS. Blood. 47(1). 99–112. 21 indexed citations

16.

Vella, Francis, et al.. (1974). Hemoglobin St. Claude or α2127 (H10) Lys → Thrβ2. Biochimica et Biophysica Acta (BBA) - Protein Structure. 365(2). 318–322. 17 indexed citations

17.

Huisman, TH, et al.. (1968). Oxygen equilibria studies of the hemoglobins from normal and anemic sheep and goats. American Journal of Physiology-Legacy Content. 215(1). 140–146. 41 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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