Mariëlle Alders

9.9k total citations
114 papers, 4.0k citations indexed

About

Mariëlle Alders is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Mariëlle Alders has authored 114 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 47 papers in Genetics and 35 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Mariëlle Alders's work include Cardiac electrophysiology and arrhythmias (29 papers), Genetic Syndromes and Imprinting (21 papers) and Epigenetics and DNA Methylation (20 papers). Mariëlle Alders is often cited by papers focused on Cardiac electrophysiology and arrhythmias (29 papers), Genetic Syndromes and Imprinting (21 papers) and Epigenetics and DNA Methylation (20 papers). Mariëlle Alders collaborates with scholars based in Netherlands, United States and United Kingdom. Mariëlle Alders's co-authors include Arthur A.M. Wilde, Marcel M. A. M. Mannens, Irene M. van Langen, Raoul C. M. Hennekam, Jet Bliek, Nynke Hofman, Michael J. Ackerman, David J. Tester, Benjamin A. Salisbury and Hanno L. Tan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and Nature Genetics.

In The Last Decade

Mariëlle Alders

110 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mariëlle Alders Netherlands	36	2.1k	1.6k	1.2k	494	364	114	4.0k
Amy E. Roberts United States	33	3.2k 1.5×	979 0.6×	797 0.7×	227 0.5×	461 1.3×	87	4.6k
Mary Ella Pierpont United States	36	3.9k 1.8×	726 0.5×	1.6k 1.3×	507 1.0×	1.2k 3.3×	98	6.0k
Stephanie M. Ware United States	35	3.1k 1.4×	1.4k 0.9×	1.1k 0.9×	294 0.6×	900 2.5×	141	4.9k
M. Cristina Digilio Italy	43	3.9k 1.8×	530 0.3×	2.1k 1.7×	344 0.7×	721 2.0×	248	5.9k
Edward Blair United Kingdom	27	1.6k 0.8×	1.4k 0.9×	1.2k 1.0×	259 0.5×	348 1.0×	47	3.5k
Cecilia Camacho‐Hübner United Kingdom	38	1.8k 0.8×	592 0.4×	1.5k 1.3×	791 1.6×	627 1.7×	103	5.0k
Alexander A.L. Jorge Brazil	36	2.0k 1.0×	330 0.2×	1.7k 1.4×	330 0.7×	467 1.3×	185	3.8k
Kim L. McBride United States	30	1.3k 0.6×	563 0.4×	807 0.7×	209 0.4×	267 0.7×	108	2.7k
Sally Ann Lynch Ireland	34	1.6k 0.8×	177 0.1×	1.4k 1.2×	379 0.8×	744 2.0×	146	3.7k
Patricia A. Ward United States	25	1.0k 0.5×	233 0.1×	1.2k 1.0×	627 1.3×	161 0.4×	65	2.5k

Countries citing papers authored by Mariëlle Alders

Since Specialization

Citations

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

Fields of papers citing papers by Mariëlle Alders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mariëlle Alders

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Elinck, Ellen, Jasper J. van der Smagt, Mariëlle Alders, et al.. (2024). Loss-of-function of activity-dependent neuroprotective protein (ADNP) by a splice-acceptor site mutation causes Helsmoortel–Van der Aa syndrome. European Journal of Human Genetics. 32(6). 630–638. 4 indexed citations

Postma, Alex V., Christina Rapp, Katrin Knoflach, et al.. (2023). Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension. SHILAP Revista de lepidopterología. 1(1). 100811–100811. 1 indexed citations

Rooney, Kathleen, Sadegheh Haghshenas, Haley McConkey, et al.. (2023). Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature. International Journal of Molecular Sciences. 24(18). 14240–14240. 3 indexed citations

Henneman, Peter, et al.. (2022). Prenatal Neun+ Neurons of Down Syndrome Display Aberrant Integrative DNA Methylation and Gene Expression Profiles. Epigenomics. 14(7). 375–390.

Sparago, Angela, Andrea Freschi, Saskia M. Maas, et al.. (2019). Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus. Genetics in Medicine. 21(8). 1808–1820. 32 indexed citations

Ivanovski, Ivan, Marzia Pollazzon, Stefano Giuseppe Caraffi, et al.. (2018). Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes. American Journal of Medical Genetics Part A. 176(5). 1166–1174. 13 indexed citations

Sollis, Elliot, Pelagia Derizioti, Hirotomo Saitsu, et al.. (2017). Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders. Human Mutation. 38(11). 1542–1554. 30 indexed citations

Chatzispyrou, Iliana A., Mariëlle Alders, Sergio Guerrero‐Castillo, et al.. (2017). A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome. Human Molecular Genetics. 26(13). 2541–2550. 56 indexed citations

Alders, Mariëlle, Hennie Bikker, & Imke Christiaans. (2015). Long QT Syndrome. 13 indexed citations

10.

Alders, Mariëlle, Saskia M. Maas, D.J. Kadouch, et al.. (2014). Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood. European Journal of Medical Genetics. 57(6). 293–297. 20 indexed citations

11.

Matthijs, Gert, Mariëlle Alders, Peter Bauer, et al.. (2014). EuroGentest guidelines for diagnostic next generation sequencing. European Journal of Human Genetics. 22. 566–566. 3 indexed citations

12.

Spaendonck‐Zwarts, Karin Y. van, Maarten P. van den Berg, Denise Hilfiker‐Kleiner, et al.. (2014). Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy. European Heart Journal. 35(32). 2165–2173. 126 indexed citations

13.

Hersmus, Remko, Yvonne G. van der Zwan, Hans Stoop, et al.. (2012). A 46,XY Female DSD Patient with Bilateral Gonadoblastoma, a Novel SRY Missense Mutation Combined with a WT1 KTS Splice-Site Mutation. PLoS ONE. 7(7). e40858–e40858. 27 indexed citations

14.

Giudicessi, John R., Jamie D. Kapplinger, David J. Tester, et al.. (2012). Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-QT Syndrome. Circulation Cardiovascular Genetics. 5(5). 519–528. 44 indexed citations

15.

Etheridge, Susan P., Neil E. Bowles, Cammon B. Arrington, et al.. (2011). Somatic mosaicism contributes to phenotypic variation in Timothy syndrome. American Journal of Medical Genetics Part A. 155(10). 2578–2583. 43 indexed citations

16.

Hollink, Iris H.I.M., Marry M. van den Heuvel‐Eibrink, Martin Zimmermann, et al.. (2009). Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia. Blood. 113(23). 5951–5960. 80 indexed citations

17.

Postema, Pieter G., Irene M. van Langen, Eline A. Nannenberg, et al.. (2007). Genetische identificatie van patiënten en families met lange-QT-syndroom: Grote regionale verschillen in de resultaten van 10 jaar. Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank. 151(11). 644–648. 3 indexed citations

18.

Alders, Mariëlle, Andy Ryan, Matt Hodges, et al.. (2000). Disruption of a Novel Imprinted Zinc-Finger Gene, ZNF215, in Beckwith-Wiedemann Syndrome. The American Journal of Human Genetics. 66(5). 1473–1484. 40 indexed citations

19.

Oudejans, Cees B.M., Bart A. Westerman, Andrea A.M. Könst, et al.. (1997). Growth regulation of extraembryonic tissues. European Journal of Obstetrics & Gynecology and Reproductive Biology. 75(1). 29–32. 2 indexed citations

20.

Alders, Mariëlle, Matt Hodges, Anna‐Katerina Hadjantonakis, et al.. (1997). The Human Achaete-Scute Homologue 2 (ASCL2, HASH2) Maps to Chromosome 11p15.5, Close to IGF2 and is Expressed in Extravillus Trophoblasts. Human Molecular Genetics. 6(6). 859–867. 69 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.

Explore authors with similar magnitude of impact