A citation-based method for searching scientific literature

Nicole I Wolf, Charles Ffrench-Constant, Marjo S van der Knaap. Nat Rev Neurol 2021
Times Cited: 32







List of co-cited articles
239 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Invited article: an MRI-based approach to the diagnosis of white matter disorders.
Raphael Schiffmann, Marjo S van der Knaap. Neurology 2009
342
18

Suppression of proteolipid protein rescues Pelizaeus-Merzbacher disease.
Matthew S Elitt, Lilianne Barbar, H Elizabeth Shick, Berit E Powers, Yuka Maeno-Hikichi, Mayur Madhavan, Kevin C Allan, Baraa S Nawash, Artur S Gevorgyan, Stevephen Hung,[...]. Nature 2020
23
26

Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophy.
Geneviève Bernard, Eliane Chouery, Maria Lisa Putorti, Martine Tétreault, Asako Takanohashi, Giovanni Carosso, Isabelle Clément, Odile Boespflug-Tanguy, Diana Rodriguez, Valérie Delague,[...]. Am J Hum Genet 2011
165
18

Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy.
Marisa I Mendes, Mariana Gutierrez Salazar, Kether Guerrero, Isabelle Thiffault, Gajja S Salomons, Laurence Gauquelin, Luan T Tran, Diane Forget, Marie-Soleil Gauthier, Quinten Waisfisz,[...]. Am J Hum Genet 2018
45
18


Recessive mutations in POLR3B, encoding the second largest subunit of Pol III, cause a rare hypomyelinating leukodystrophy.
Martine Tétreault, Karine Choquet, Simona Orcesi, Davide Tonduti, Umberto Balottin, Martin Teichmann, Sébastien Fribourg, Raphael Schiffmann, Bernard Brais, Adeline Vanderver,[...]. Am J Hum Genet 2011
104
15

Case definition and classification of leukodystrophies and leukoencephalopathies.
Adeline Vanderver, Morgan Prust, Davide Tonduti, Fanny Mochel, Heather M Hussey, Guy Helman, James Garbern, Florian Eichler, Pierre Labauge, Patrick Aubourg,[...]. Mol Genet Metab 2015
140
15


Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity.
Ryan J Taft, Adeline Vanderver, Richard J Leventer, Stephen A Damiani, Cas Simons, Sean M Grimmond, David Miller, Johanna Schmidt, Paul J Lockhart, Kate Pope,[...]. Am J Hum Genet 2013
128
15

Diagnosis, prognosis, and treatment of leukodystrophies.
Marjo S van der Knaap, Raphael Schiffmann, Fanny Mochel, Nicole I Wolf. Lancet Neurol 2019
52
15

The molecular pathogenesis of Pelizaeus-Merzbacher disease.
J Garbern, F Cambi, M Shy, J Kamholz. Arch Neurol 1999
95
15

An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex.
Ye Zhang, Kenian Chen, Steven A Sloan, Mariko L Bennett, Anja R Scholze, Sean O'Keeffe, Hemali P Phatnani, Paolo Guarnieri, Christine Caneda, Nadine Ruderisch,[...]. J Neurosci 2014
15

Lentiviral haemopoietic stem-cell gene therapy in early-onset metachromatic leukodystrophy: an ad-hoc analysis of a non-randomised, open-label, phase 1/2 trial.
Maria Sessa, Laura Lorioli, Francesca Fumagalli, Serena Acquati, Daniela Redaelli, Cristina Baldoli, Sabrina Canale, Ignazio D Lopez, Francesco Morena, Andrea Calabria,[...]. Lancet 2016
290
12

Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients.
Samuel Groeschel, Jörn-Sven Kühl, Annette E Bley, Christiane Kehrer, Bernhard Weschke, Michaela Döring, Judith Böhringer, Johanna Schrum, René Santer, Alfried Kohlschütter,[...]. JAMA Neurol 2016
61
12

Developmental outcomes of cord blood transplantation for Krabbe disease: A 15-year study.
Matthew D Wright, Michele D Poe, Anthony DeRenzo, Shilpa Haldal, Maria L Escolar. Neurology 2017
55
12

Magnetic resonance imaging pattern recognition in hypomyelinating disorders.
Marjan E Steenweg, Adeline Vanderver, Susan Blaser, Alberto Bizzi, Tom J de Koning, Grazia M S Mancini, Wessel N van Wieringen, Frederik Barkhof, Nicole I Wolf, Marjo S van der Knaap. Brain 2010
184
12

Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism.
Hussein Daoud, Martine Tétreault, William Gibson, Kether Guerrero, Ana Cohen, Janina Gburek-Augustat, Matthis Synofzik, Bernard Brais, Cathy A Stevens, Rocio Sanchez-Carpintero,[...]. J Med Genet 2013
74
12

Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations.
Nicole I Wolf, Adeline Vanderver, Rosalina M L van Spaendonk, Raphael Schiffmann, Bernard Brais, Marianna Bugiani, Erik Sistermans, Coriene Catsman-Berrevoets, Johan M Kros, Pedro Soares Pinto,[...]. Neurology 2014
115
12

Assembly of CNS myelin in the absence of proteolipid protein.
M Klugmann, M H Schwab, A Pühlhofer, A Schneider, F Zimmermann, I R Griffiths, K A Nave. Neuron 1997
339
12

The CNS Myelin Proteome: Deep Profile and Persistence After Post-mortem Delay.
Olaf Jahn, Sophie B Siems, Kathrin Kusch, Dörte Hesse, Ramona B Jung, Thomas Liepold, Marina Uecker, Ting Sun, Hauke B Werner. Front Cell Neurosci 2020
27
14

Congenital cardiac anomalies and white matter injury.
Paul D Morton, Nobuyuki Ishibashi, Richard A Jonas, Vittorio Gallo. Trends Neurosci 2015
37
12

Axonal selection and myelin sheath generation in the central nervous system.
Mikael Simons, David A Lyons. Curr Opin Cell Biol 2013
62
12


BIG1/Arfgef1 and Arf1 regulate the initiation of myelination by Schwann cells in mice.
Yuki Miyamoto, Tomohiro Torii, Kenji Tago, Akito Tanoue, Shou Takashima, Junji Yamauchi. Sci Adv 2018
31
12

PP1C and PP2A are p70S6K Phosphatases Whose Inhibition Ameliorates HLD12-Associated Inhibition of Oligodendroglial Cell Morphological Differentiation.
Naoto Matsumoto, Yuki Miyamoto, Kohei Hattori, Akihiro Ito, Hironori Harada, Hiroaki Oizumi, Katsuya Ohbuchi, Kazushige Mizoguchi, Junji Yamauchi. Biomedicines 2020
7
57

The Infantile Leukoencephalopathy-Associated Mutation of C11ORF73/HIKESHI Proteins Generates de novo Interactive Activity with Filamin A, Inhibiting Oligodendroglial Cell Morphological Differentiation.
Kohei Hattori, Kenji Tago, Shiori Memezawa, Arisa Ochiai, Sui Sawaguchi, Yukino Kato, Takanari Sato, Kazuma Tomizuka, Hiroaki Ooizumi, Katsuya Ohbuchi,[...]. Medicines (Basel) 2021
5
80

VCAM1 acts in parallel with CD69 and is required for the initiation of oligodendrocyte myelination.
Yuki Miyamoto, Tomohiro Torii, Akito Tanoue, Junji Yamauchi. Nat Commun 2016
34
12


Myelin dynamics: protecting and shaping neuronal functions.
Aiman S Saab, Klaus-Armin Nave. Curr Opin Neurobiol 2017
104
12

Mutations in POLR3A and POLR3B encoding RNA Polymerase III subunits cause an autosomal-recessive hypomyelinating leukoencephalopathy.
Hirotomo Saitsu, Hitoshi Osaka, Masayuki Sasaki, Jun-Ichi Takanashi, Keisuke Hamada, Akio Yamashita, Hidehiro Shibayama, Masaaki Shiina, Yukiko Kondo, Kiyomi Nishiyama,[...]. Am J Hum Genet 2011
109
9

Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy.
Alessandra Biffi, Eugenio Montini, Laura Lorioli, Martina Cesani, Francesca Fumagalli, Tiziana Plati, Cristina Baldoli, Sabata Martino, Andrea Calabria, Sabrina Canale,[...]. Science 2013
800
9

Long-Term Safety, Immunologic Response, and Imaging Outcomes following Neural Stem Cell Transplantation for Pelizaeus-Merzbacher Disease.
Nalin Gupta, Roland G Henry, Sang-Mo Kang, Jonathan Strober, Daniel A Lim, Tamara Ryan, Rachel Perry, Jody Farrell, Mary Ulman, Raja Rajalingam,[...]. Stem Cell Reports 2019
23
13

Transplantation of umbilical-cord blood in babies with infantile Krabbe's disease.
Maria L Escolar, Michele D Poe, James M Provenzale, Karen C Richards, June Allison, Susan Wood, David A Wenger, Daniel Pietryga, Donna Wall, Martin Champagne,[...]. N Engl J Med 2005
478
9

Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation.
Imen Dorboz, Hélene Dumay-Odelot, Karima Boussaid, Yosra Bouyacoub, Pauline Barreau, Simon Samaan, Haifa Jmel, Eleonore Eymard-Pierre, Claude Cances, Céline Bar,[...]. Neurol Genet 2018
36
9

A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies.
Sumit Parikh, Geneviève Bernard, Richard J Leventer, Marjo S van der Knaap, Johan van Hove, Amy Pizzino, Nathan H McNeill, Guy Helman, Cas Simons, Johanna L Schmidt,[...]. Mol Genet Metab 2015
117
9

Estimating the relative frequency of leukodystrophies and recommendations for carrier screening in the era of next-generation sequencing.
Johanna L Schmidt, Amy Pizzino, Jessica Nicholl, Allison Foley, Yue Wang, Jill A Rosenfeld, Lindsey Mighion, Lora Bean, Cristina da Silva, Megan T Cho,[...]. Am J Med Genet A 2020
12
25


Oligodendroglia metabolically support axons and contribute to neurodegeneration.
Youngjin Lee, Brett M Morrison, Yun Li, Sylvain Lengacher, Mohamed H Farah, Paul N Hoffman, Yiting Liu, Akivaga Tsingalia, Lin Jin, Ping-Wu Zhang,[...]. Nature 2012
984
9

Whole exome sequencing in patients with white matter abnormalities.
Adeline Vanderver, Cas Simons, Guy Helman, Joanna Crawford, Nicole I Wolf, Geneviève Bernard, Amy Pizzino, Johanna L Schmidt, Asako Takanohashi, David Miller,[...]. Ann Neurol 2016
90
9

Mutations in RARS cause hypomyelination.
Nicole I Wolf, Gajja S Salomons, Richard J Rodenburg, Petra J W Pouwels, Jolanda H Schieving, Terry G J Derks, Johanna M Fock, Patrick Rump, Daphne M van Beek, Marjo S van der Knaap,[...]. Ann Neurol 2014
73
9

Neurodevelopmental outcomes of umbilical cord blood transplantation in metachromatic leukodystrophy.
Holly R Martin, Michele D Poe, James M Provenzale, Joanne Kurtzberg, Adam Mendizabal, Maria L Escolar. Biol Blood Marrow Transplant 2013
72
9

Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia.
Julia M Edgar, Mark McLaughlin, Donald Yool, Su-Chun Zhang, Jill H Fowler, Paul Montague, Jennifer A Barrie, Mailis C McCulloch, Ian D Duncan, James Garbern,[...]. J Cell Biol 2004
227
9


Axonal swellings and degeneration in mice lacking the major proteolipid of myelin.
I Griffiths, M Klugmann, T Anderson, D Yool, C Thomson, M H Schwab, A Schneider, F Zimmermann, M McCulloch, N Nadon,[...]. Science 1998
628
9

Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation.
James Y Garbern, Donald A Yool, Gregory J Moore, Ian B Wilds, Michael W Faulk, Matthias Klugmann, Klaus-Amin Nave, Erik A Sistermans, Marjo S van der Knaap, Thomas D Bird,[...]. Brain 2002
203
9

Altered human oligodendrocyte heterogeneity in multiple sclerosis.
Sarah Jäkel, Eneritz Agirre, Ana Mendanha Falcão, David van Bruggen, Ka Wai Lee, Irene Knuesel, Dheeraj Malhotra, Charles Ffrench-Constant, Anna Williams, Gonçalo Castelo-Branco. Nature 2019
290
9

Maintenance of high proteolipid protein level in adult central nervous system myelin is required to preserve the integrity of myelin and axons.
Katja A Lüders, Stefan Nessler, Kathrin Kusch, Julia Patzig, Ramona B Jung, Wiebke Möbius, Klaus-Armin Nave, Hauke B Werner. Glia 2019
20
15

Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity.
Ursula Fünfschilling, Lotti M Supplie, Don Mahad, Susann Boretius, Aiman S Saab, Julia Edgar, Bastian G Brinkmann, Celia M Kassmann, Iva D Tzvetanova, Wiebke Möbius,[...]. Nature 2012
865
9


Genetic dissection of oligodendroglial and neuronal Plp1 function in a novel mouse model of spastic paraplegia type 2.
Katja A Lüders, Julia Patzig, Mikael Simons, Klaus-Armin Nave, Hauke B Werner. Glia 2017
24
12


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.