Annick Raas‐Rothschild

6.5k total citations
108 papers, 3.8k citations indexed

About

Annick Raas‐Rothschild is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Annick Raas‐Rothschild has authored 108 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 36 papers in Genetics and 33 papers in Physiology. Recurrent topics in Annick Raas‐Rothschild's work include Lysosomal Storage Disorders Research (28 papers), Calcium signaling and nucleotide metabolism (16 papers) and Cellular transport and secretion (11 papers). Annick Raas‐Rothschild is often cited by papers focused on Lysosomal Storage Disorders Research (28 papers), Calcium signaling and nucleotide metabolism (16 papers) and Cellular transport and secretion (11 papers). Annick Raas‐Rothschild collaborates with scholars based in Israel, United States and France. Annick Raas‐Rothschild's co-authors include Ruth Bargal, Gideon Bach, Thomas Braulke, Marcia Zeigler, Ayala Frumkin, Nili Avidan, Anthony H. Futerman, Gustavo Glusman, Doron Lancet and Edna Ben‐Asher and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Medicine.

In The Last Decade

Annick Raas‐Rothschild

105 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Annick Raas‐Rothschild Israel 34 1.7k 982 898 781 661 108 3.8k
Anna‐Elina Lehesjoki Finland 39 2.1k 1.3× 1.4k 1.4× 1.6k 1.7× 943 1.2× 226 0.3× 126 4.9k
Ingo Kurth Germany 31 1.6k 1.0× 486 0.5× 399 0.4× 838 1.1× 167 0.3× 110 3.5k
Cynthia J. Tifft United States 30 1.9k 1.1× 1.5k 1.5× 1.2k 1.4× 724 0.9× 250 0.4× 111 4.0k
Yoji Hakamata Japan 30 1.9k 1.1× 198 0.2× 666 0.7× 182 0.2× 295 0.4× 129 3.5k
Catherine Caillaud France 32 1.5k 0.9× 2.1k 2.1× 789 0.9× 803 1.0× 163 0.2× 107 3.6k
Laurie Erb United States 43 1.8k 1.1× 818 0.8× 264 0.3× 147 0.2× 3.1k 4.7× 69 4.4k
Claudio Bruno Italy 37 3.3k 2.0× 588 0.6× 426 0.5× 697 0.9× 77 0.1× 146 4.6k
Kinga Szigeti United States 24 933 0.6× 450 0.5× 239 0.3× 427 0.5× 95 0.1× 64 2.9k
Marwan Shinawi United States 32 2.4k 1.4× 751 0.8× 1.5k 1.7× 257 0.3× 54 0.1× 137 4.3k
Gheona Altarescu Israel 29 795 0.5× 2.1k 2.1× 361 0.4× 848 1.1× 220 0.3× 126 3.4k

Countries citing papers authored by Annick Raas‐Rothschild

Since Specialization
Citations

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

Fields of papers citing papers by Annick Raas‐Rothschild

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Annick Raas‐Rothschild. 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 Annick Raas‐Rothschild. The network helps show where Annick Raas‐Rothschild may publish in the future.

Co-authorship network of co-authors of Annick Raas‐Rothschild

This figure shows the co-authorship network connecting the top 25 collaborators of Annick Raas‐Rothschild. A scholar is included among the top collaborators of Annick Raas‐Rothschild 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 Annick Raas‐Rothschild. Annick Raas‐Rothschild 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.
Baker, Elizabeth, Ben Pode‐Shakked, Laura Cross, et al.. (2022). PPP2R1A neurodevelopmental disorder is associated with congenital heart defects. American Journal of Medical Genetics Part A. 188(11). 3262–3277. 7 indexed citations
2.
Gabis, Lidia V., Shahar Shefer, & Annick Raas‐Rothschild. (2020). Ethical Dilemmas Linked to Fragile X Testing of Minors—a Preliminary Survey Among Professionals. Journal of Molecular Neuroscience. 70(2). 254–259. 2 indexed citations
3.
Pode‐Shakked, Ben, et al.. (2020). Shared facial phenotype of patients with mucolipidosis type IV: A clinical observation reaffirmed by next generation phenotyping. European Journal of Medical Genetics. 63(7). 103927–103927. 9 indexed citations
4.
Batzir, Nurit Assia, Jennifer E. Posey, Xiaofei Song, et al.. (2019). Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome). American Journal of Medical Genetics Part A. 182(1). 38–52. 30 indexed citations
5.
Elizur, Shai E., Michal Berkenstadt, Noah Gruber, et al.. (2018). [FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?]. PubMed. 157(4). 241–244. 1 indexed citations
6.
Vivante, Asaf, Hadas Ityel, Ben Pode‐Shakked, et al.. (2017). Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases. Pediatric Nephrology. 32(12). 2273–2282. 27 indexed citations
7.
Kämpe, Anders, Alice Costantini, Yael Levy‐Shraga, et al.. (2017). PLS3 Deletions Lead to Severe Spinal Osteoporosis and Disturbed Bone Matrix Mineralization. Journal of Bone and Mineral Research. 32(12). 2394–2404. 36 indexed citations
8.
Reinstein, Eyal, Ana Gutiérrez‐Fernández, Shay Tzur, et al.. (2016). Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C. European Journal of Human Genetics. 24(12). 1792–1796. 33 indexed citations
9.
Sukenik‐Halevy, Rivka, Mark D. Ludman, Shay Ben‐Shachar, & Annick Raas‐Rothschild. (2015). The time-consuming demands of the practice of medical genetics in the era of advanced genomic testing. Genetics in Medicine. 18(4). 372–377. 33 indexed citations
10.
Jamra, Rami Abou, Annick Raas‐Rothschild, Sebastian Eck, et al.. (2011). Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature. The American Journal of Human Genetics. 88(6). 788–795. 167 indexed citations
11.
Kohn, Yoav, et al.. (2010). Psychiatric and cognitive profile in Anderson‐Fabry patients: a preliminary study. Journal of Inherited Metabolic Disease. 33(4). 429–436. 20 indexed citations
12.
Moskovitz, Moti, et al.. (2006). Dental management of a child with trisomy 9 mosaicism: a case report.. PubMed. 28(3). 265–8. 4 indexed citations
13.
14.
Molinari, Florence, Annick Raas‐Rothschild, Marlène Rio, et al.. (2005). Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy. The American Journal of Human Genetics. 76(2). 334–339. 115 indexed citations
15.
Dagoneau, Nathalie, Déborah Scheffer, Céline Huber, et al.. (2004). Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome. The American Journal of Human Genetics. 74(2). 298–305. 136 indexed citations
16.
Perles, Zeev, Amiram Nir, M. Nadjari, et al.. (2003). Absent Ductus venosus in the Fetus: Review of the Literature and First Report of Direct Umbilical Venous Drainage to the Coronary Sinus. Fetal Diagnosis and Therapy. 18(4). 247–251. 24 indexed citations
17.
Falik‐Zaccai, Tzipora C., et al.. (2003). Mucolipidosis III type C: first‐trimester biochemical and molecular prenatal diagnosis. Prenatal Diagnosis. 23(3). 211–214. 6 indexed citations
18.
Nir, Amiram, et al.. (2001). Rhabdomyoma in the Fetus: Illustration of Tumor Growth During the Second Half of Gestation. Pediatric Cardiology. 22(6). 515–518. 20 indexed citations
19.
Raas‐Rothschild, Annick, Valérie Cormier‐Daire, Ming Bao, et al.. (2000). Molecular basis of variant pseudo-Hurler polydystrophy (mucolipidosis IIIC). Journal of Clinical Investigation. 105(5). 673–681. 136 indexed citations
20.
Berkenstadt, Michal, et al.. (1990). Megalocornea, macrocephaly, mental and motor retardation (MMMM). Clinical Genetics. 38(2). 149–154. 16 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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