Annick Raas‐Rothschild

6.5k citations

108 papers · 3.8k indexed · h-index 34

Molecular Biology top 5%
Physiology top 2%
Genetics top 2%
Cell Biology top 1%
Physiology top 0.2%

Co-authors: Ruth Bargal Gideon Bach Thomas Braulke Marcia Zeigler Ayala Frumkin Nili Avidan Anthony H. Futerman Edna Ben‐Asher
Topics: Lysosomal Storage Disorders Research (28 papers)Calcium signaling and nucleotide metabolism (16 papers)Cellular transport and secretion (11 papers)
Cited by: Physiology Sensory Systems Cell Biology
Journals: Journal of Biological Chemistry Journal of Clinical Investigation Nature Medicine
Partner nations: Israel United States France

In The Last Decade

Annick Raas‐Rothschild

105 papers receiving 3.7k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	PPP2R1A neurodevelopmental disorder is associated with congenital heart defects 2022 ·American Journal of Medical Genetics Part A ·Elizabeth Baker,(unknown),Ben Pode‐Shakked,Laura Cross,Bonnie Sullivan,Annick Raas‐Rothschild,(unknown),Ortal Barel,Omer Bar‐Yosef,Ammar Husami,Robert J. Hopkin,Carlos E. Prada,Rolf W. Stottmann,K. Nicole Weaver	7
2	Ethical Dilemmas Linked to Fragile X Testing of Minors—a Preliminary Survey Among Professionals 2020 ·Journal of Molecular Neuroscience ·Lidia V. Gabis,Shahar Shefer,Annick Raas‐Rothschild	2
3	Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome) 2019 ·American Journal of Medical Genetics Part A ·Nurit Assia Batzir,Jennifer E. Posey,Xiaofei Song,Zeynep Coban‐Akdemir,Jill A. Rosenfeld,Chester Brown,Emily Chen,(unknown),(unknown),(unknown),Katelyn Payne,Annick Raas‐Rothschild,Richard H. Scott,Hilary J. Vernon,Neda Zadeh,James R. Lupski,V. Reid Sutton	30
4	[FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?] 2018 ·PubMed ·Shai E. Elizur,Michal Berkenstadt,(unknown),Noah Gruber,Orit Pinhas‐Hamiel,Sharon Hassin‐Baer,Annick Raas‐Rothschild,Hila Raanani,Tali Cukierman‐Yaffe,Raoul Orvieto,Yoram Cohen,Lidia V. Gabis	1
5	Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C 2016 ·European Journal of Human Genetics ·Eyal Reinstein,Ana Gutiérrez‐Fernández,Shay Tzur,Concetta Bormans,Shai Marcu,Einav Tayeb-Fligelman,Chana Vinkler,Annick Raas‐Rothschild,(unknown),Meytal Landau,Mordechai Shohat,Xosé S. Puente,Doron M. Behar,Carlos López-Otı́n	33
6	The time-consuming demands of the practice of medical genetics in the era of advanced genomic testing 2015 ·Genetics in Medicine ·Rivka Sukenik‐Halevy,Mark D. Ludman,Shay Ben‐Shachar,Annick Raas‐Rothschild	33
7	Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature 2011 ·The American Journal of Human Genetics ·Rami Abou Jamra,(unknown),Annick Raas‐Rothschild,Sebastian Eck,Elisabeth Graf,Rebecca Buchert,Guntram Borck,Arif B. Ekici,Felix F. Brockschmidt,Markus M. Nöthen,Arnold Münnich,Tim M. Strom,André Reis,Laurence Colleaux	167
8	The clinical spectrum of fetal Niemann–Pick type C 2009 ·American Journal of Medical Genetics Part A ·Ronen Spiegel,Annick Raas‐Rothschild,Orit Reish,(unknown),Vardiella Meiner,Ruth Bargal,(unknown),Karen Meir,Michel Nadjari,Gratiana Hermann,(unknown),Stavit A. Shalev,Marsha Zeigler	68
9	Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications 2008 ·The American Journal of Human Genetics ·Ruth Bargal,Valérie Cormier‐Daire,Ziva Ben‐Neriah,Martine Le Merrer,Jacob Sosna,Judith Melki,David Zangen,Sarah Smithson,Zvi Borochowitz,Ruth Belostotsky,Annick Raas‐Rothschild	82
10	Dental management of a child with trisomy 9 mosaicism: a case report. 2006 ·PubMed ·Moti Moskovitz,(unknown),Annick Raas‐Rothschild	4
11	Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy 2005 ·The American Journal of Human Genetics ·Florence Molinari,Annick Raas‐Rothschild,Marlène Rio,Giuseppe Fiermonte,Férechté Encha‐Razavi,Luigi Palmieri,Ferdinando Palmieri,Ziva Ben‐Neriah,Noman Kadhom,Michel Vekemans,Tania Attié‐Bitach,Arnold Münnich,Pierre Rustin,Laurence Colleaux	115
12	Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization of 11 cases 2005 ·American Journal of Medical Genetics Part A ·Manuela Morleo,Tiziano Pramparo,Lucia Perone,Giuliana Gregato,Cédric Le Caignec,Robert F. Mueller,Tsutomu Ogata,Annick Raas‐Rothschild,(unknown),Louise C. Wilson,Gerald W. Zaidman,Orsetta Zuffardi,Andrea Ballabio,Brunella Franco	26
13	Mucolipidosis II is caused by mutations in GNPTA encoding the α/β GlcNAc-1-phosphotransferase 2005 ·Nature Medicine ·Stephan Tiede,Stephan Storch,Torben Lübke,Bernard Henrissat,Ruth Bargal,Annick Raas‐Rothschild,Thomas Braulke	146
14	Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome 2004 ·The American Journal of Human Genetics ·Nathalie Dagoneau,Déborah Scheffer,Céline Huber,L.I. Al-Gazali,Maja Di Rocco,Anne Godard,Jelena Martinović,Annick Raas‐Rothschild,Sabine Sigaudy,Sheila Unger,Sophie Nicole,Bertrand Fontaine,Jean‐Luc Taupin,Jean-François Moreau,Andrea Superti‐Furga,Martine Le Merrer,Jacky Bonaventure,Arnold Münnich,Laurence Legeai‐Mallet,Valérie Cormier‐Daire	136
15	Glycosphingolipidoses: Beyond the enzymatic defect 2004 ·Glycoconjugate Journal ·Annick Raas‐Rothschild,Irene Pankova-Kholmyansky,(unknown),Anthony H. Futerman	36
16	Mucolipidosis III type C: first‐trimester biochemical and molecular prenatal diagnosis 2003 ·Prenatal Diagnosis ·Tzipora C. Falik‐Zaccai,M. Zeigler,Ruth Bargal,Gideon Bach,(unknown),Annick Raas‐Rothschild	6
17	Rhabdomyoma in the Fetus: Illustration of Tumor Growth During the Second Half of Gestation 2001 ·Pediatric Cardiology ·Amiram Nir,(unknown),M. Nadjari,Annick Raas‐Rothschild,Azaria J.J.T. Rein	20
18	Molecular basis of variant pseudo-Hurler polydystrophy (mucolipidosis IIIC) 2000 ·Journal of Clinical Investigation ·Annick Raas‐Rothschild,Valérie Cormier‐Daire,Ming Bao,Emmanuelle Génin,Rémi Salomon,Kevin Brewer,Marsha Zeigler,Hanna Mandel,(unknown),Bruce A. Roe,Arnold Munnich,William M. Canfield	136
19	Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: A new variant 1993 ·The Journal of Pediatrics ·(unknown),Annick Raas‐Rothschild,Meena Upadhyaya,Moshe Frydman,I Sarova-Pinhàs,(unknown),(unknown)	12
20	Megalocornea, macrocephaly, mental and motor retardation (MMMM) 1990 ·Clinical Genetics ·(unknown),Michal Berkenstadt,Annick Raas‐Rothschild,Richard M. Goodman	16

About Annick Raas‐Rothschild

Annick Raas‐Rothschild is a scholar working on Physiology, Developmental Biology and Genetics, having authored 108 papers that have together received 3.8k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (28 papers), Calcium signaling and nucleotide metabolism (16 papers) and Cellular transport and secretion (11 papers). The work is most often cited by research in Physiology (661 citations), Sensory Systems (290 citations) and Cell Biology (781 citations). Annick Raas‐Rothschild has collaborated with scholars based in Israel, United States and France. Frequent co-authors include Ruth Bargal, Gideon Bach, Thomas Braulke, Marcia Zeigler, Ayala Frumkin, Nili Avidan, Anthony H. Futerman, Edna Ben‐Asher, Gustavo Glusman and Doron Lancet. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Medicine.

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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