Marianne Till

4.9k total citations
61 papers, 1.2k citations indexed

About

Marianne Till is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marianne Till has authored 61 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 25 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marianne Till's work include Genomic variations and chromosomal abnormalities (31 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Prenatal Screening and Diagnostics (12 papers). Marianne Till is often cited by papers focused on Genomic variations and chromosomal abnormalities (31 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Prenatal Screening and Diagnostics (12 papers). Marianne Till collaborates with scholars based in France, United States and Germany. Marianne Till's co-authors include Patrick Edery, Damien Sanlaville, Audrey Labalme, Arnold Münnich, Stanislas Lyonnet, Gaëtan Lesca, Caroline Schluth‐Bolard, Anna Pelet, Jeanne Amiel and Tania Attié‐Bitach and has published in prestigious journals such as Environmental Health Perspectives, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Marianne Till

57 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marianne Till France 17 659 556 223 194 97 61 1.2k
Emmanuelle Lemyre Canada 22 879 1.3× 550 1.0× 129 0.6× 276 1.4× 61 0.6× 52 1.3k
Séverine Drunat France 21 443 0.7× 581 1.0× 150 0.7× 144 0.7× 160 1.6× 57 1.1k
Patricia I. Bader United States 18 584 0.9× 619 1.1× 94 0.4× 180 0.9× 49 0.5× 32 1.1k
Rita Genesio Italy 19 463 0.7× 496 0.9× 92 0.4× 204 1.1× 52 0.5× 52 998
Alice Goldenberg France 20 565 0.9× 678 1.2× 100 0.4× 91 0.5× 75 0.8× 49 1.1k
Daniela del Gaudio United States 18 1.0k 1.5× 854 1.5× 254 1.1× 388 2.0× 55 0.6× 47 1.8k
Katrin Õunap Estonia 25 857 1.3× 1.0k 1.8× 75 0.3× 264 1.4× 126 1.3× 106 1.8k
Anna Lindstrand Sweden 22 827 1.3× 882 1.6× 89 0.4× 135 0.7× 134 1.4× 84 1.5k
Elisabetta Lapi Italy 18 477 0.7× 534 1.0× 70 0.3× 131 0.7× 43 0.4× 48 957
Annalisa Vetro Italy 20 552 0.8× 524 0.9× 73 0.3× 203 1.0× 43 0.4× 51 1.0k

Countries citing papers authored by Marianne Till

Since Specialization
Citations

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

Fields of papers citing papers by Marianne Till

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marianne Till

This figure shows the co-authorship network connecting the top 25 collaborators of Marianne Till. A scholar is included among the top collaborators of Marianne Till 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 Marianne Till. Marianne Till 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.
Hanna, Nadine, Sophie Dupuis‐Girod, Marianne Till, et al.. (2020). A Case of Trisomy 13 Mosaicism Presenting with a Severe Aortic Root Dilatation and Marfanoid Habitus due to an Unpredictable Cytogenetic Mechanism. Cytogenetic and Genome Research. 160(2). 72–79.
2.
Poulat, Anne‐Lise, Nicolas Chatron, Audrey Labalme, et al.. (2019). Asparagine synthetase deficiency: A novel case with an unusual molecular mechanism. Molecular Genetics and Metabolism Reports. 21. 100509–100509. 6 indexed citations
3.
Labalme, Audrey, Marianne Till, Gérald Bussy, et al.. (2018). Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations. Clinical Case Reports. 6(5). 827–834. 3 indexed citations
4.
Alix, Eudéline, et al.. (2017). Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric Sequences. Cytogenetic and Genome Research. 153(3). 117–124. 2 indexed citations
5.
Louvrier, Camille, Audrey Labalme, Vincent des Portes, et al.. (2015). Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7. Cytogenetic and Genome Research. 147(2-3). 111–117. 14 indexed citations
6.
Plotton, Ingrid, et al.. (2014). Normal Value of Steroids in Amniotic Fluid by LC-MS/MS Method. 82. 1 indexed citations
7.
Pons, Linda, Audrey Labalme, Marianne Till, et al.. (2014). A new syndrome of intellectual disability with dysmorphism due to TBL1XR1 deletion. American Journal of Medical Genetics Part A. 167(1). 164–168. 35 indexed citations
8.
Boutry‐Kryza, Nadia, Audrey Labalme, Dorothée Ville, et al.. (2014). Molecular characterization of a cohort of 73 patients with infantile spasms syndrome. European Journal of Medical Genetics. 58(2). 51–58. 51 indexed citations
9.
Putoux, Audrey, Audrey Labalme, Jean‐Marie André, et al.. (2013). Jacobsen and Beckwith–Wiedemann syndromes in a child with mosaicism for partial 11pter trisomy and partial 11qter monosomy. American Journal of Medical Genetics Part A. 161(2). 331–337. 13 indexed citations
10.
Redin, Claire, Stéphanie Le Gras, Véronique Geoffroy, et al.. (2012). Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes. Journal of Medical Genetics. 49(8). 502–512. 81 indexed citations
11.
Rossi, Massimiliano, Audrey Labalme, Marie‐Pierre Cordier, et al.. (2012). Mosaic 18q21.2 deletions including the TCF4 gene: A clinical report. American Journal of Medical Genetics Part A. 158A(12). 3174–3181. 10 indexed citations
12.
Boutry‐Kryza, Nadia, Audrey Labalme, Marianne Till, et al.. (2011). An 800 kb deletion at 17q23.2 including the MED13 (THRAP1) gene, revealed by aCGH in a patient with a SMC 17p. American Journal of Medical Genetics Part A. 158A(2). 400–405. 16 indexed citations
13.
Lesca, Gaëtan, Marianne Till, Audrey Labalme, et al.. (2011). De novo Xq11.11 microdeletion including ARHGEF9 in a boy with mental retardation, epilepsy, macrosomia, and dysmorphic features. American Journal of Medical Genetics Part A. 155(7). 1706–1711. 32 indexed citations
14.
Schluth‐Bolard, Caroline, Damien Sanlaville, Audrey Labalme, et al.. (2010). 17p13.1 microdeletion involving the TP53 gene in a boy presenting with mental retardation but no tumor. American Journal of Medical Genetics Part A. 152A(5). 1278–1282. 29 indexed citations
15.
Schluth‐Bolard, Caroline, Marianne Till, Patrick Edery, & Damien Sanlaville. (2008). Syndromes chromosomiques émergents. Pathologie Biologie. 56(6). 380–387. 3 indexed citations
16.
André, Emmanuel, Marianne Till, Pascal Descargues, et al.. (2005). Le syndrome de Netherton : une ectodermatose du petit nourrisson avec retard de croissance, déficit immunitaire et rachitisme. À propos de 3 cas. Archives de Pédiatrie. 12(9). 1364–1367. 6 indexed citations
17.
18.
Amiel, Jeanne, Yolanda Espinosa‐Parrilla, Julie Steffann, et al.. (2001). Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures. The American Journal of Human Genetics. 69(6). 1370–1377. 79 indexed citations
19.
Guffon, Nathalie, Christine Vianey‐Saban, Marianne Till, et al.. (1993). [Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings].. PubMed. 48(5). 365–71. 1 indexed citations
20.
Till, Marianne, et al.. (1991). Duplication of chromosome 11 centromere in fetal and maternal karyotypes: A new variant?. Prenatal Diagnosis. 11(7). 481–482. 2 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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