Muriel Holder

4.8k total citations
14 papers, 408 citations indexed

About

Muriel Holder is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Muriel Holder has authored 14 papers receiving a total of 408 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Cell Biology. Recurrent topics in Muriel Holder's work include Cellular transport and secretion (3 papers), Blood disorders and treatments (2 papers) and Lysosomal Storage Disorders Research (2 papers). Muriel Holder is often cited by papers focused on Cellular transport and secretion (3 papers), Blood disorders and treatments (2 papers) and Lysosomal Storage Disorders Research (2 papers). Muriel Holder collaborates with scholars based in France, United Kingdom and United States. Muriel Holder's co-authors include Pierre Sarda, M. Durand, Vincent Marion, Sabine Sigaudy, Hélène Dollfus, Christian P. Hamel, Bruno Moulin, Christian Brandt, Corinne Stoetzel and Anne‐Françoise Roux and has published in prestigious journals such as Blood, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Muriel Holder

14 papers receiving 406 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Muriel Holder France	9	283	185	92	26	25	14	408
Tobias Eisenberger Germany	11	437 1.5×	165 0.9×	75 0.8×	66 2.5×	7 0.3×	14	531
Bellinda van den Helm Netherlands	11	320 1.1×	201 1.1×	36 0.4×	31 1.2×	15 0.6×	17	465
Zohreh Fattahi Iran	12	300 1.1×	112 0.6×	158 1.7×	42 1.6×	28 1.1×	36	459
Michael J. Dixon United Kingdom	9	263 0.9×	172 0.9×	92 1.0×	8 0.3×	35 1.4×	11	461
Ali Muhammad Waryah Pakistan	12	191 0.7×	77 0.4×	150 1.6×	38 1.5×	24 1.0×	39	412
Cynthia C. Morton United States	8	178 0.6×	81 0.4×	150 1.6×	26 1.0×	9 0.4×	8	407
Flavia Palombo Italy	10	226 0.8×	155 0.8×	18 0.2×	27 1.0×	18 0.7×	27	416
Joanna Wiszniewska United States	12	348 1.2×	360 1.9×	15 0.2×	27 1.0×	43 1.7×	22	607
Susana Cañón Spain	13	487 1.7×	73 0.4×	81 0.9×	94 3.6×	16 0.6×	18	668
C Bützler Germany	8	511 1.8×	88 0.5×	84 0.9×	37 1.4×	16 0.6×	10	646

Countries citing papers authored by Muriel Holder

Since Specialization

Citations

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

Fields of papers citing papers by Muriel Holder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muriel Holder

This figure shows the co-authorship network connecting the top 25 collaborators of Muriel Holder. A scholar is included among the top collaborators of Muriel Holder 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 Muriel Holder. Muriel Holder 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

1.

Matthew, Jacqueline, Maria Deprez, Alena Uus, et al.. (2019). OC11.08: Syndromic craniofacial dysmorphic feature assessment in utero: potential for a novel imaging methodology with reconstructed 3D fetal MRI models. Ultrasound in Obstetrics and Gynecology. 54(S1). 29–29. 2 indexed citations

2.

Walt, Jon van der, et al.. (2015). Case Report: Congenital Erythroleukemia in a Premature Infant with Dysmorphic Features. Pediatric and Developmental Pathology. 19(4). 334–337. 1 indexed citations

3.

Pepermans, Elise, Vincent Michel, Richard J. Goodyear, et al.. (2014). The CD 2 isoform of protocadherin‐15 is an essential component of the tip‐link complex in mature auditory hair cells. EMBO Molecular Medicine. 6(7). 984–992. 54 indexed citations

4.

Masurel‐Paulet, Alice, Isabelle Drumare, Muriel Holder, et al.. (2014). Further delineation of eye manifestations in homozygous 15q13.3 microdeletions including TRPM1: A differential diagnosis of ceroid lipofuscinosis. American Journal of Medical Genetics Part A. 164(6). 1537–1544. 18 indexed citations

5.

Mention-Mulliez, Karine, et al.. (2013). Five Year Follow-Up of Two Sisters With Type II Sialidosis: Systemic and Ophthalmic Findings Including OCT Analysis. Journal of Pediatric Ophthalmology & Strabismus. 50(6). e33–6. 9 indexed citations

6.

Mau‐Them, Frédéric Tran, Marjolaine Willems, Beate Albrecht, et al.. (2013). Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability. European Journal of Human Genetics. 22(2). 289–292. 30 indexed citations

7.

Rieder, Mark J., Glenn E. Green, Sarah S. Park, et al.. (2012). A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome. The American Journal of Human Genetics. 91(2). 397–397. 6 indexed citations

8.

Rieder, Mark J., Glenn E. Green, Sarah S. Park, et al.. (2012). A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome. The American Journal of Human Genetics. 90(5). 907–914. 67 indexed citations

9.

Trujillo‐Quintero, Juan Pablo, Leonardo Mina, Roser Pujol, et al.. (2012). On the role of FAN1 in Fanconi anemia. Blood. 120(1). 86–89. 27 indexed citations

10.

Moradkhani, Kamran, Michel Bahuau, Muriel Holder, et al.. (2011). Practical approach for characterization of glucose 6‐phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: Description of seven new G6PD mutants. American Journal of Hematology. 87(2). 208–210. 8 indexed citations

11.

Rakza, Thameur, et al.. (2011). Choanal Atresia Associated With Tracheoesophageal Fistula: The Spectrum of Carbimazole Embryopathy. PEDIATRICS. 128(3). e703–e706. 6 indexed citations

12.

Marion, Vincent, Corinne Stoetzel, M. Durand, et al.. (2010). Bardet-Biedl Syndrome. Clinical Journal of the American Society of Nephrology. 6(1). 22–29. 91 indexed citations

13.

Baux, David, Lise Larrieu, Catherine Blanchet, et al.. (2007). Molecular and in silico analyses of the full-length isoform of usherin identify new pathogenic alleles in Usher type II patients. Human Mutation. 28(8). 781–789. 86 indexed citations

14.

Dieux‐Coëslier, Anne, Alexandre Moerman, Muriel Holder, et al.. (2003). Metaphyseal chondrodysplasia with cone‐shaped epiphyses: A specific form involving the lower limbs. American Journal of Medical Genetics Part A. 124A(1). 60–66. 3 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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