Miriam Goedbloed

2.2k total citations
19 papers, 1.3k citations indexed

About

Miriam Goedbloed is a scholar working on Molecular Biology, Physiology and Oncology. According to data from OpenAlex, Miriam Goedbloed has authored 19 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Physiology and 7 papers in Oncology. Recurrent topics in Miriam Goedbloed's work include Tuberous Sclerosis Complex Research (10 papers), Histiocytic Disorders and Treatments (6 papers) and Polyomavirus and related diseases (6 papers). Miriam Goedbloed is often cited by papers focused on Tuberous Sclerosis Complex Research (10 papers), Histiocytic Disorders and Treatments (6 papers) and Polyomavirus and related diseases (6 papers). Miriam Goedbloed collaborates with scholars based in Netherlands, United States and Germany. Miriam Goedbloed's co-authors include Mark Nellist, Dicky Halley, Őzgür Sancak, Ans M.W. van den Ouweland, Anneke Maat‐Kievit, Ans van den Ouweland, Senno Verhoef, Carine Wouters, Bernard A. Zonnenberg and Peter Elfferich and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Neurology.

In The Last Decade

Miriam Goedbloed

19 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Miriam Goedbloed Netherlands 15 609 600 326 254 97 19 1.3k
Annika E. Wallberg Sweden 20 225 0.4× 1.4k 2.4× 288 0.9× 202 0.8× 58 0.6× 29 1.8k
Tazuko Hirai United States 8 394 0.6× 848 1.4× 97 0.3× 177 0.7× 20 0.2× 8 1.1k
Taegun Kwon United States 12 332 0.5× 616 1.0× 62 0.2× 74 0.3× 29 0.3× 18 959
Anwaar Ahmad United States 9 174 0.3× 811 1.4× 111 0.3× 154 0.6× 82 0.8× 13 1.1k
Antonia Tomás‐Loba Spain 7 386 0.6× 805 1.3× 60 0.2× 300 1.2× 21 0.2× 9 1.1k
Anthony Vertino United States 9 65 0.1× 476 0.8× 274 0.8× 140 0.6× 79 0.8× 11 762
J. A. Rillema United States 16 78 0.1× 509 0.8× 226 0.7× 231 0.9× 38 0.4× 72 973
Linda J. Swanson United States 14 322 0.5× 300 0.5× 48 0.1× 183 0.7× 34 0.4× 20 906
Karin Kroboth United Kingdom 14 203 0.3× 465 0.8× 93 0.3× 131 0.5× 86 0.9× 17 1.4k
Ningling Kang‐Decker United States 7 104 0.2× 573 1.0× 156 0.5× 117 0.5× 36 0.4× 7 970

Countries citing papers authored by Miriam Goedbloed

Since Specialization
Citations

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

Fields of papers citing papers by Miriam Goedbloed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miriam Goedbloed

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

All Works

19 of 19 papers shown
1.
Cankar, Katarina, Adèle van Houwelingen, Miriam Goedbloed, et al.. (2014). Valencene oxidase CYP706M1 from Alaska cedar (Callitropsis nootkatensis). FEBS Letters. 588(6). 1001–1007. 47 indexed citations
2.
Dong, Lemeng, Karel Miettinen, Miriam Goedbloed, et al.. (2013). Characterization of two geraniol synthases from Valeriana officinalis and Lippia dulcis: Similar activity but difference in subcellular localization. Metabolic Engineering. 20. 198–211. 72 indexed citations
3.
Liu, Qing, Mohammad Majdi, Katarina Cankar, et al.. (2011). Reconstitution of the Costunolide Biosynthetic Pathway in Yeast and Nicotiana benthamiana. PLoS ONE. 6(8). e23255–e23255. 108 indexed citations
4.
Goedbloed, Miriam, Mark Vermeulen, Rixun Fang, et al.. (2009). Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit. International Journal of Legal Medicine. 123(6). 471–482. 110 indexed citations
5.
Corach, Daniel, Óscar Lao, Cecilia Bobillo, et al.. (2009). Inferring Continental Ancestry of Argentineans from Autosomal, Y‐Chromosomal and Mitochondrial DNA. Annals of Human Genetics. 74(1). 65–76. 128 indexed citations
6.
Nellist, Mark, Őzgür Sancak, Miriam Goedbloed, et al.. (2008). Functional characterisation of the TSC1–TSC2 complex to assess multiple TSC2 variants identified in single families affected by tuberous sclerosis complex. BMC Medical Genetics. 9(1). 10–10. 16 indexed citations
7.
Nellist, Mark, Diana van den Heuvel, Miriam Goedbloed, et al.. (2008). Missense mutations to the TSC1 gene cause tuberous sclerosis complex. European Journal of Human Genetics. 17(3). 319–328. 21 indexed citations
8.
Nellist, Mark, Őzgür Sancak, Miriam Goedbloed, et al.. (2005). Large Deletion at the TSC1 Locus in a Family with Tuberous Sclerosis Complex. Genetic Testing. 9(3). 226–230. 8 indexed citations
9.
Sancak, Őzgür, Mark Nellist, Miriam Goedbloed, et al.. (2005). Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype – phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex. European Journal of Human Genetics. 13(6). 731–741. 344 indexed citations
10.
Nellist, Mark, Őzgür Sancak, Miriam Goedbloed, et al.. (2004). Distinct effects of single amino-acid changes to tuberin on the function of the tuberin–hamartin complex. European Journal of Human Genetics. 13(1). 59–68. 65 indexed citations
11.
Mayer, Karin, et al.. (2004). Characterisation of a novel TSC2 missense mutation in the GAP related domain associated with minimal clinical manifestations of tuberous sclerosis. Journal of Medical Genetics. 41(5). e64–e64. 36 indexed citations
12.
Jansen, Floor E., Robbert G. E. Notenboom, Mark Nellist, et al.. (2004). Differential localization of hamartin and tuberin and increased S6 phosphorylation in a tuber. Neurology. 63(7). 1293–1295. 21 indexed citations
13.
Nellist, Mark, Miriam Goedbloed, & D. J. J. Halley. (2003). Regulation of tuberous sclerosis complex (TSC) function by 14-3-3 proteins. Biochemical Society Transactions. 31(3). 587–591. 23 indexed citations
14.
Nellist, Mark, Miriam Goedbloed, Brenda Verhaaf, et al.. (2002). Identification and Characterization of the Interaction between Tuberin and 14-3-3ζ. Journal of Biological Chemistry. 277(42). 39417–39424. 64 indexed citations
15.
Goedbloed, Miriam, Mark Nellist, Brenda Verhaaf, et al.. (2001). Analysis of TSC2 stop codon variants found in tuberous sclerosis patients. European Journal of Human Genetics. 9(11). 823–828. 7 indexed citations
16.
Nauta, Jeroen, et al.. (2000). Immunological detection of polycystin-1 in human kidney. Histochemistry and Cell Biology. 113(4). 303–311. 12 indexed citations
17.
Nauta, Jeroen, Miriam Goedbloed, H. van Herck, et al.. (2000). New Rat Model that Phenotypically Resembles Autosomal Recessive Polycystic Kidney Disease. Journal of the American Society of Nephrology. 11(12). 2272–2284. 26 indexed citations
18.
Nellist, Mark, Marjon A. van Slegtenhorst, Miriam Goedbloed, et al.. (1999). Characterization of the Cytosolic Tuberin-Hamartin Complex. Journal of Biological Chemistry. 274(50). 35647–35652. 148 indexed citations
19.
Goedbloed, Miriam, et al.. (1997). The Han:SPRD rat is not a genetic model of human autosomal dominant polycystic kidney disease type 1. Laboratory Animals. 31(3). 241–247. 7 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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