Nine Knoers

6.5k total citations
66 papers, 2.4k citations indexed

About

Nine Knoers is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Nine Knoers has authored 66 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 35 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Nine Knoers's work include Genomics and Rare Diseases (16 papers), Ion Transport and Channel Regulation (12 papers) and Renal and related cancers (12 papers). Nine Knoers is often cited by papers focused on Genomics and Rare Diseases (16 papers), Ion Transport and Channel Regulation (12 papers) and Renal and related cancers (12 papers). Nine Knoers collaborates with scholars based in Netherlands, United States and United Kingdom. Nine Knoers's co-authors include Gijs van Haaften, Mieke M. van Haelst, L.A.H. Monnens, Helen I. Roessler, Heleen H. Arts, Marian Verdijk, Eva H. Brilstra, Ans M.W. van den Ouweland, Bernard A. van Oost and Isaäc J. Nijman and has published in prestigious journals such as Nature Genetics, Blood and PEDIATRICS.

In The Last Decade

Nine Knoers

64 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nine Knoers Netherlands 31 1.3k 830 336 331 263 66 2.4k
Kathleen Freson Belgium 34 1.3k 1.0× 705 0.8× 282 0.8× 435 1.3× 208 0.8× 143 3.6k
Marwan Shinawi United States 32 2.4k 1.8× 1.5k 1.8× 226 0.7× 375 1.1× 176 0.7× 137 4.3k
Vassili Valayannopoulos France 39 1.5k 1.1× 562 0.7× 173 0.5× 595 1.8× 117 0.4× 125 4.7k
Emil Kakkis United States 37 1.1k 0.8× 582 0.7× 169 0.5× 184 0.6× 124 0.5× 73 5.0k
Rossella Parini Italy 38 1.5k 1.1× 533 0.6× 137 0.4× 299 0.9× 113 0.4× 179 5.1k
Nathalie Guffon France 35 1.2k 0.9× 348 0.4× 214 0.6× 296 0.9× 89 0.3× 138 6.5k
Chester B. Whitley United States 39 1.6k 1.2× 894 1.1× 132 0.4× 352 1.1× 74 0.3× 201 5.1k
Bruno Bembi Italy 43 1.4k 1.0× 313 0.4× 140 0.4× 162 0.5× 210 0.8× 133 5.4k
Ni‐Chung Lee Taiwan 33 1.7k 1.3× 798 1.0× 129 0.4× 373 1.1× 274 1.0× 218 4.3k
Brendan J. Keating United States 28 909 0.7× 823 1.0× 107 0.3× 234 0.7× 95 0.4× 102 2.8k

Countries citing papers authored by Nine Knoers

Since Specialization
Citations

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

Fields of papers citing papers by Nine Knoers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nine Knoers

This figure shows the co-authorship network connecting the top 25 collaborators of Nine Knoers. A scholar is included among the top collaborators of Nine 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 Nine Knoers. Nine Knoers 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.
Tibben, Aad, et al.. (2024). Hope, but never expect? Comparing parents' pre‐ and post‐disclosure attitudes toward return of results from diagnostic exome sequencing for their child. Molecular Genetics & Genomic Medicine. 12(3). e2341–e2341. 1 indexed citations
2.
Snoek, Rozemarijn, Rieke van der Graaf, Kitty W.M. Bloemenkamp, et al.. (2020). Pregnancy in Advanced Kidney Disease: Clinical Practice Considerations on a Challenging Combination. ˜The œNephron journals/Nephron journals. 144(4). 185–189. 10 indexed citations
3.
Lochmüller, Hanns, Rachel Thompson, Nine Knoers, et al.. (2018). RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases. European Journal of Human Genetics. 26(6). 778–785. 37 indexed citations
4.
Baas, Annette F., Wilko Spiering, Frans L. Moll, et al.. (2016). Six uneventful pregnancy outcomes in an extended vascular Ehlers–Danlos syndrome family. American Journal of Medical Genetics Part A. 173(2). 519–523. 5 indexed citations
5.
Monroe, Glen R., G. W. J. Frederix, Sanne M. C. Savelberg, et al.. (2016). Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability. Genetics in Medicine. 18(9). 949–956. 125 indexed citations
6.
Knoers, Nine, et al.. (2016). Phenotypic familial aggregation in chronic chilblains. Family Practice. 33(5). 461–465. 3 indexed citations
7.
Baaij, Jeroen H. F. de, Eiske M. Dorresteijn, Eric A. M. Hennekam, et al.. (2015). Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia. Nephrology Dialysis Transplantation. 30(6). 952–957. 41 indexed citations
8.
Munnik, Sonja A. de, Jolt Roukema, Jeroen Schoots, et al.. (2015). Meier-Gorlin syndrome. Orphanet Journal of Rare Diseases. 10(1). 114–114. 58 indexed citations
9.
Boers, Sarah N., Johannes J. M. van Delden, Nine Knoers, & Annelien L. Bredenoord. (2015). Postmortem disclosure of genetic information to family members: active or passive?. Trends in Molecular Medicine. 21(3). 148–153. 13 indexed citations
10.
Kroes, Hester Y., Glen R. Monroe, Bert van der Zwaag, et al.. (2015). Joubert syndrome: genotyping a Northern European patient cohort. European Journal of Human Genetics. 24(2). 214–220. 50 indexed citations
11.
Donker, Albertine E., Reinier Raymakers, Natasja Dors, et al.. (2014). Practice guidelines for the diagnosis and management of microcytic anemias due to genetic disorders of iron metabolism or heme synthesis. Blood. 123(25). 3873–3886. 49 indexed citations
12.
Hussain, Sofia, Naomi Issler, Nicholas Lench, et al.. (2013). KCNJ10 Mutations Display Differential Sensitivity to Heteromerisation with KCNJ16. Nephron Physiology. 123(3-4). 7–14. 31 indexed citations
13.
Munnik, Sonja A. de, Sixto García‐Miñáur, Alexander Hoischen, et al.. (2013). A de novo non-sense mutation in ZBTB18 in a patient with features of the 1q43q44 microdeletion syndrome. European Journal of Human Genetics. 22(6). 844–846. 36 indexed citations
14.
Lichtenbelt, Klaske D., Nine Knoers, & G. Heleen Schuring‐Blom. (2011). From Karyotyping to Array-CGH in Prenatal Diagnosis. Cytogenetic and Genome Research. 135(3-4). 241–250. 49 indexed citations
15.
Vermeer, Sascha, Rowdy Meijer, Janneke Timmermans, et al.. (2008). ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia. Neurogenetics. 9(3). 207–214. 105 indexed citations
16.
Robben, Joris H., Mozes Sze, Nine Knoers, & Peter M.T. Deen. (2005). Rescue of Vasopressin V2 Receptor Mutants by Chemical Chaperones: Specificity and Mechanism. Molecular Biology of the Cell. 17(1). 379–386. 77 indexed citations
17.
Weber, Stefanie, Katrin Hoffmann, Nikola Jeck, et al.. (2000). Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene. European Journal of Human Genetics. 8(6). 414–422. 78 indexed citations
18.
Knoers, Nine & P.M.T. Deen. (1998). Aquaporin molecular biology and clinical abnormalities of the water transport channels. Current Opinion in Pediatrics. 10(4). 428–434. 6 indexed citations
19.
Odermatt, Alex, Peter E.M. Taschner, Stephen W. Scherer, et al.. (1997). Characterization of the Gene Encoding Human Sarcolipin (SLN), a Proteolipid Associated with SERCA1: Absence of Structural Mutations in Five Patients with Brody Disease. Genomics. 45(3). 541–553. 125 indexed citations
20.
Knoers, Nine, Ans M.W. van den Ouweland, Marian Verdijk, L.A.H. Monnens, & Bernard A. van Oost. (1994). Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidus. Kidney International. 46(1). 170–176. 45 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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