Marie-Odile Rolland

1.8k citations

39 papers · 1.3k indexed · h-index 20

Molecular Biology top 10%
Clinical Biochemistry top 1%
Pulmonary and Respiratory Medicine top 10%
Physiology top 10%
Pediatrics, Perinatology and Child Health top 5%

Co-authors: Pierre Cochat Stéphane Blanche Alain Fischer Sonia Fargue P. Divry A. Liutkus Jean‐Louis Chaussain C Griscelli
Topics: Metabolism and Genetic Disorders (19 papers)Diet and metabolism studies (6 papers)Kidney Stones and Urolithiasis Treatments (5 papers)
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: New England Journal of Medicine JNCI Journal of the National Cancer Institute Annals of Neurology
Partner nations: France United States Japan

In The Last Decade

Marie-Odile Rolland

39 papers receiving 1.2k citations

Peers

Countries citing papers authored by Marie-Odile Rolland

Since Specialization

Citations

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

Fields of papers citing papers by Marie-Odile Rolland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie-Odile Rolland. 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 Marie-Odile Rolland. The network helps show where Marie-Odile Rolland may publish in the future.

Co-authorship network of co-authors of Marie-Odile Rolland

This figure shows the co-authorship network connecting the top 25 collaborators of Marie-Odile Rolland. A scholar is included among the top collaborators of Marie-Odile Rolland 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 Marie-Odile Rolland. Marie-Odile Rolland 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	Muscle phosphorylase b kinase deficiency revisited 2010 ·Neuromuscular Disorders ·Andoni Echaniz‐Laguna,Hasan O. Akman,Michel Mohr,Christine Tranchant,(unknown),Marie-Odile Rolland,Salvatore DiMauro	25
2	Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1 2009 ·Kidney International ·Sonia Fargue,Jérôme Harambat,Marie‐France Gagnadoux,Michel Tsimaratos,Françoise Janssen,Brigitte Llanas,(unknown),B. Boudailliez,Gérard Champion,C. Guyot,Marie‐Alice Macher,Hubert Nivet,Bruno Ranchin,Rémi Salomon,Sophie Taque,Marie-Odile Rolland,Pierre Cochat	51
3	Déficit en 3-HMG-CoA lyase à révélation tardive : savoir reconnaître une maladie rare mais traitable 2009 ·Archives de Pédiatrie ·(unknown),(unknown),(unknown),(unknown),Guy Touati,(unknown),Marie-Odile Rolland,Cécile Acquaviva	5
4	Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome 2009 ·Kidney International ·Jérôme Harambat,Sonia Fargue,Cécile Acquaviva,Marie‐France Gagnadoux,Françoise Janssen,A. Liutkus,Chebl Mourani,Marie‐Alice Macher,Daniel Abramowicz,Christophe Legendre,Antoine Dürrbach,Michel Tsimaratos,Hubert Nivet,Éric Girardin,Anne‐Marie Schott,Marie-Odile Rolland,Pierre Cochat	109
5	Primary hyperoxaluria type 1: still challenging! 2006 ·Pediatric Nephrology ·Pierre Cochat,A. Liutkus,Sonia Fargue,(unknown),Bruno Ranchin,Marie-Odile Rolland	91
6	A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency 2006 ·Molecular Genetics and Metabolism ·Toshiyuki Fukao,(unknown),Marie-Odile Rolland,M. T. Zabot,Andreas Schulze,Keitaro Yamada,Naomi Kondo	18
7	A case of pyruvate carboxylase deficiency with atypical clinical and neuroradiological presentation 2005 ·Molecular Genetics and Metabolism ·Melissa A. Schiff,Virginie Levrat,Cécile Acquaviva,Christine Vianey‐Saban,Marie-Odile Rolland,Nathalie Guffon	15
8	Mitochondrial Acetoacetyl-CoA Thiolase (T2) Deficiency: T2-Deficient Patients with “Mild” Mutation(s) Were Previously Misinterpreted as Normal by the Coupled Assay with Tiglyl-CoA 2004 ·Pediatric Research ·(unknown),Toshiyuki Fukao,Marie-Odile Rolland,M. T. Zabot,(unknown),(unknown),Masashi Kondo,Naoki Matsuo,Naomi Kondo	29
9	The E37X is a common HMGCL mutation in Portuguese patients with 3-hydroxy-3-methylglutaric CoA lyase deficiency 2004 ·Molecular Genetics and Metabolism ·Maria Luı́s Cardoso,(unknown),Elisa Leão Teles,Esmeralda Martins,Luísa Diogo,Esmeralda Rodrigues,Paula Garcia,Marie-Odile Rolland,Laura Vilarinho	24
10	Randomized Controlled Trial of Once- Versus Thrice-Daily Tobramycin in Febrile Neutropenic Children Undergoing Stem Cell Transplantation 2003 ·JNCI Journal of the National Cancer Institute ·Lillian Sung,L. Lee Dupuis,B P Bliss,Anna Taddio,Mohamed Abdolell,Upton Allen,Marie-Odile Rolland,Allison Tong,Tracey Taylor,John Doyle	18
11	Seventeen novel mutations that cause profound biotinidase deficiency 2002 ·Molecular Genetics and Metabolism ·Barry Wolf,Kevin P. Jensen,(unknown),Mübeccel Demirkol,T. Baykal,P. Divry,Marie-Odile Rolland,Celia Pérez‐Cerdá,Magdalena Ugarte,Rachel Straussberg,Lina Basel‐Vanagaite,E. R. Baumgartner,Terttu Suormala,Sabine Scholl,Anibh M. Das,S. Schweitzer,Ewa Pronicka,Jolanta Sykut‐Cegielska	31
12	Primary hyperoxaluria in infants: Medical, ethical, and economic issues 1999 ·The Journal of Pediatrics ·Pierre Cochat,Paulo César Koch Nogueira,(unknown),Neville V. Jamieson,Jon I. Scheinman,Marie-Odile Rolland	55
13	Combined liver-kidney transplantation in primary hyperoxaluria type 1 1999 ·European Journal of Pediatrics ·Pierre Cochat,Jean‐Michel Gaulier,Paulo César Koch Nogueira,Janusz Feber,Neville V. Jamieson,Marie-Odile Rolland,P. Divry,Dominique Bozon,Laurence Dubourg	59
14	Clinical approach to inherited peroxisomal disorders: A series of 27 patients 1998 ·Annals of Neurology ·Matthias R. Baumgartner,Bwee Tien Poll‐The,Nanda M. Verhoeven,C. Jakobs,Marc Espeel,Frank Roels,Daniel Rabier,Thierry Levade,Marie-Odile Rolland,Maria Carmen Martínez,R. J. A. Wanders,Jean Marie Saudubray	41
15	Two Missense Point Mutations in Different Alleles in the 3-Hydroxy-3-methylglutaryl Coenzyme A Lyase Gene Produce 3-Hydroxy-3-methylglutaric Aciduria in a French Patient 1998 ·Archives of Biochemistry and Biophysics ·(unknown),Juan Pié,Jorge Lloberas,Marie-Odile Rolland,B. Leroux,M. Vidailhet,P. Divry,Fausto G. Hegardt,Núria Casals	11
16	Mutations in the pterin-4α-carbinolamine dehydratase ( PCBD ) gene cause a benign form of hyperphenylalaninemia 1998 ·Human Genetics ·Beat Thöny,(unknown),L. Kierat,Marie-Odile Rolland,P Guibaud,(unknown),(unknown),Randall A. Heidenreich,M. Durán,J. B. C. de Klerk,June E. Ayling,Nenad Blau	30
17	A 13-bp deletion (1952 del 13) in the methylmalonyl CoA mutase gene of an affected patient 1995 ·Human Mutation ·(unknown),Marie-Odile Rolland,P. Divry,Monique Mathieu,P Guibaud,Dominique Bozon	5
18	Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear family 1995 ·Human Molecular Genetics ·Nathalie Nadal,Marie-Odile Rolland,Christine Tranchant,Laurence Reutenauer,Gàbor Gyapay,Jean‐Marie Warter,Jean‐Louis Mandel,M. Kœnig	17
19	Mevalonic aciduria in 3 siblings: A new recognizable metabolic encephalopathy 1993 ·Pediatric Neurology ·Josette Mancini,Nicole Philip,B. Chabrol,P. Divry,Marie-Odile Rolland,N Pinsard	19
20	Comparison of Red Cell Transfusion and Polyethylene Glycol-Modified Adenosine Deaminase Therapy in an Adenosine Deaminase-Deficient Child: Measurement of Erythrocyte Deoxyadenosine Triphosphate as a Useful Tool 1990 ·Pediatric Research ·C. Bory,Roselyne Boulieu,G Souillet,(unknown),Marie-Odile Rolland,M. Mathieu,Michael S. Hershfield	16

About Marie-Odile Rolland

Marie-Odile Rolland is a scholar working on Clinical Biochemistry, Biochemistry and Pediatrics, Perinatology and Child Health, having authored 39 papers that have together received 1.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (19 papers), Diet and metabolism studies (6 papers) and Kidney Stones and Urolithiasis Treatments (5 papers). The work is most often cited by research in Clinical Biochemistry (385 citations), Biochemistry (89 citations) and Molecular Biology (756 citations). Marie-Odile Rolland has collaborated with scholars based in France, United States and Japan. Frequent co-authors include Pierre Cochat, Stéphane Blanche, Alain Fischer, Sonia Fargue, P. Divry, A. Liutkus, Jean‐Louis Chaussain, C Griscelli, Isabelle Jambaqué and G. Kalifa. Their work appears in journals such as New England Journal of Medicine, JNCI Journal of the National Cancer Institute and Annals of Neurology.

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