Lia Spruit

696 total citations
8 papers, 516 citations indexed

About

Lia Spruit is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lia Spruit has authored 8 papers receiving a total of 516 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Lia Spruit's work include Genetic and Kidney Cyst Diseases (7 papers), Renal and related cancers (6 papers) and Genetic Syndromes and Imprinting (5 papers). Lia Spruit is often cited by papers focused on Genetic and Kidney Cyst Diseases (7 papers), Renal and related cancers (6 papers) and Genetic Syndromes and Imprinting (5 papers). Lia Spruit collaborates with scholars based in Netherlands, United Kingdom and Australia. Lia Spruit's co-authors include Dorien J.M. Peters, Jasper J. Saris, Martijn H. Breuning, Hans G. Dauwerse, David Ravine, M.H. Breuning, Emile de Heer, Jan A. Bruijn, Constantinos Deltas and Barbera Veldhuisen and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and The Journal of Pathology.

In The Last Decade

Lia Spruit

8 papers receiving 502 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lia Spruit Netherlands	7	432	339	81	50	49	8	516
Patrick G. Starremans United States	9	349 0.8×	438 1.3×	141 1.7×		28 0.6×	10	547
Georgia I. Anyatonwu United States	8	396 0.9×	336 1.0×	212 2.6×		27 0.6×	10	526
Qian Feng China	2	475 1.1×	404 1.2×	182 2.2×		38 0.8×	6	557
Sekiya Shibazaki United States	3	450 1.0×	381 1.1×	145 1.8×		32 0.7×	5	491
Seema Kapoor India	11	62 0.1×	157 0.5×	26 0.3×	5 0.1×	37 0.8×	40	283
Sharon Mulroy United Kingdom	5	275 0.6×	244 0.7×	79 1.0×		26 0.5×	6	353
Sandesh C. Sreenath Nagamani United States	6	218 0.5×	194 0.6×	12 0.1×	3 0.1×	70 1.4×	8	349
Eva Sammels Belgium	8	127 0.3×	273 0.8×	85 1.0×		9 0.2×	10	442
Gabriela Stangoni Italy	9	166 0.4×	122 0.4×	7 0.1×	4 0.1×	35 0.7×	24	257
Daniel R. Carvalho Brazil	11	84 0.2×	164 0.5×	12 0.1×	6 0.1×	43 0.9×	31	343

Countries citing papers authored by Lia Spruit

Since Specialization

Citations

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

Fields of papers citing papers by Lia Spruit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lia Spruit

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

All Works

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8 of 8 papers shown

1.

Ariyürek, Yavuz, et al.. (2003). Large deletions in the polycystic kidney disease 1 (PKD1) gene. Human Mutation. 23(1). 99–99. 26 indexed citations

2.

Peters, Dorien J.M., Lia Spruit, Jasper J. Saris, et al.. (1999). Cellular localization and tissue distribution of polycystin-1. The Journal of Pathology. 188(4). 439–446. 69 indexed citations

3.

Veldhuisen, Barbera, Lia Spruit, Hans G. Dauwerse, Martijn H. Breuning, & Dorien J.M. Peters. (1999). Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2). European Journal of Human Genetics. 7(8). 860–872. 63 indexed citations

4.

Roelfsema, Jeroen, Lia Spruit, Jasper J. Saris, et al.. (1997). Mutation Detection in the Repeated Part of the PKD1 Gene. The American Journal of Human Genetics. 61(5). 1044–1052. 35 indexed citations

5.

Peters, Dorien J.M., Lia Spruit, Reinhard Klingel, et al.. (1996). Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene product.. PubMed. 75(2). 221–30. 46 indexed citations

6.

Roelfsema, Jeroen, Lia Spruit, & G.J.B. van Ommen. (1994). Screening for mutations in the PKD1 gene. The American Journal of Human Genetics. 55. 1 indexed citations

7.

Peters, Dorien J.M., Lia Spruit, Jasper J. Saris, et al.. (1993). Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease. Nature Genetics. 5(4). 359–362. 192 indexed citations

8.

Breuning, M.H., Hans G. Dauwerse, G Fugazza, et al.. (1993). Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3.. PubMed. 52(2). 249–54. 84 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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