N. Knoers

687 total citations
14 papers, 454 citations indexed

About

N. Knoers is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Nephrology. According to data from OpenAlex, N. Knoers has authored 14 papers receiving a total of 454 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Pulmonary and Respiratory Medicine and 2 papers in Nephrology. Recurrent topics in N. Knoers's work include Electrolyte and hormonal disorders (7 papers), Ion Transport and Channel Regulation (7 papers) and Magnesium in Health and Disease (2 papers). N. Knoers is often cited by papers focused on Electrolyte and hormonal disorders (7 papers), Ion Transport and Channel Regulation (7 papers) and Magnesium in Health and Disease (2 papers). N. Knoers collaborates with scholars based in Netherlands, Belgium and Germany. N. Knoers's co-authors include A.F. van Lieburg, L.A.H. Monnens, Peter M.T. Deen, B. A. J. Veldman, Peter Praamstra, M.W.I.M. Horstink, Olivier Devuyst, L.A.H. Monnens, Uwe Querfeld and Thomas E. Willnow and has published in prestigious journals such as International Journal of Molecular Sciences, Journal of the American Society of Nephrology and The American Journal of Human Genetics.

In The Last Decade

N. Knoers

14 papers receiving 447 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
N. Knoers Netherlands	9	235	147	135	69	65	14	454
Pernille Bøttger Denmark	10	259 1.1×	77 0.5×	43 0.3×	122 1.8×	21 0.3×	11	490
José Ponce‐Coria Mexico	11	463 2.0×	131 0.9×	126 0.9×	72 1.0×	14 0.2×	11	570
Michelle Boone Netherlands	9	525 2.2×	302 2.1×	25 0.2×	50 0.7×	15 0.2×	11	705
Steven C. Hebert United States	10	847 3.6×	234 1.6×	94 0.7×	101 1.5×	19 0.3×	10	963
Haruki Fujisawa Japan	11	232 1.0×	115 0.8×	32 0.2×	16 0.2×	6 0.1×	37	475
Chantal Poujeol France	16	476 2.0×	129 0.9×	38 0.3×	22 0.3×	9 0.1×	27	674
Mingdao Mu China	12	113 0.5×	37 0.3×	103 0.8×	4 0.1×	23 0.4×	26	480
Nabila Boukelmoune United States	11	294 1.3×	116 0.8×	42 0.3×	18 0.3×	4 0.1×	15	500
Jin-Rui Chang China	14	152 0.6×	54 0.4×	39 0.3×	66 1.0×	5 0.1×	22	481
Vladimir A. Kashkin Russia	11	288 1.2×	67 0.5×	77 0.6×	35 0.5×	6 0.1×	28	547

Countries citing papers authored by N. Knoers

Since Specialization

Citations

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

Fields of papers citing papers by N. Knoers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N. Knoers

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

All Works

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14 of 14 papers shown

Boer, Eddy N. de, Dennis Hendriksen, Bart Charbon, et al.. (2025). Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological Disorders. International Journal of Molecular Sciences. 26(7). 2850–2850. 1 indexed citations

Boer, Eddy N. de, Nicole Corsten‐Janssen, Theo Bijma, et al.. (2025). Limitations of Semi-Automated Immunomagnetic Separation of HLA-G-Positive Trophoblasts from Papanicolaou Smears for Prenatal Genetic Diagnostics. Diagnostics. 15(3). 386–386. 1 indexed citations

Levtchenko, Elena, Gema Ariceta, Daniel G. Bichet, et al.. (2024). International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance). Nature Reviews Nephrology. 21(2). 83–96. 7 indexed citations

Knoers, N. & Albertien M. van Eerde. (2024). The Role of Genetic Testing in Adult CKD. Journal of the American Society of Nephrology. 35(8). 1107–1118. 5 indexed citations

Lange, Iris, Patrick Rump, Rinze F. Neuteboom, et al.. (2017). Male patients affected by mosaic PCDH19 mutations: five new cases. Neurogenetics. 18(3). 147–153. 36 indexed citations

Stuiver, Marchel, Sergio Laínez, Sara Terryn, et al.. (2011). CNNM2, Encoding a Basolateral Protein Required for Renal Mg2+ Handling, Is Mutated in Dominant Hypomagnesemia. The American Journal of Human Genetics. 88(3). 333–343. 150 indexed citations

Riveira‐Muñoz, Eva, Olivier Devuyst, Hendrica Belge, et al.. (2008). Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome. Nephrology Dialysis Transplantation. 23(10). 3120–3125. 12 indexed citations

Shalev, Hadar, et al.. (2004). Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus. Nephrology Dialysis Transplantation. 19(3). 608–613. 24 indexed citations

Lieburg, A.F. van, N. Knoers, & L.A.H. Monnens. (1999). Clinical Presentation and Follow-Up of 30 Patients with Congenital Nephrogenic Diabetes Insipidus. Journal of the American Society of Nephrology. 10(9). 1958–1964. 82 indexed citations

10.

Veldman, B. A. J., et al.. (1998). Genetic and environmental risk factors in Parkinson’s disease. Clinical Neurology and Neurosurgery. 100(1). 15–26. 66 indexed citations

11.

Deen, Peter M.T. & N. Knoers. (1998). Vasopressin Type-2 Receptor and Aquaporin-2 Water Channel Mutants in Nephrogenic Diabetes Insipidus. The American Journal of the Medical Sciences. 316(5). 300–309. 28 indexed citations

12.

Knoers, N., et al.. (1996). Aquaporins: from physiology to nephrogenic diabetes insipidus.. PubMed. 25. 257–73. 2 indexed citations

13.

Heuvel, Lambert P.W.J. van den, Pieter J. Westenend, Jacob van den Born, et al.. (1995). Aberrant proteoglycan composition of the glomerular basement membrane in a patient with Denys-Drash syndrome. Nephrology Dialysis Transplantation. 10(12). 2205–2211. 11 indexed citations

14.

Lieburg, A.F. van, N. Knoers, L.A.H. Monnens, & Paul Smits. (1995). Effects of arginine vasopressin and 1-desamino-8-D arginine vasopressin on forearm vasculature of healthy subjects and patients with a V2 receptor defect. Journal of Hypertension. 13(12). 1695???1700–1695???1700. 29 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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