A citation-based method for searching scientific literature

Huijie Feng, Suad Khalil, Richard R Neubig, Christos Sidiropoulos. Neurobiol Dis 2018
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Movement disorder in GNAO1 encephalopathy associated with gain-of-function mutations.
Huijie Feng, Benita Sjögren, Behirda Karaj, Vincent Shaw, Aysegul Gezer, Richard R Neubig. Neurology 2017
34
71

Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay.
Hirotomo Saitsu, Ryoko Fukai, Bruria Ben-Zeev, Yasunari Sakai, Masakazu Mimaki, Nobuhiko Okamoto, Yasuhiro Suzuki, Yukifumi Monden, Hiroshi Saito, Barak Tziperman,[...]. Eur J Hum Genet 2016
63
57

GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.
Federica Rachele Danti, Serena Galosi, Marta Romani, Martino Montomoli, Keren J Carss, F Lucy Raymond, Elena Parrini, Claudia Bianchini, Tony McShane, Russell C Dale,[...]. Neurol Genet 2017
37
57

Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
Amitha L Ananth, Amy Robichaux-Viehoever, Young-Min Kim, Andrea Hanson-Kahn, Rachel Cox, Gregory M Enns, Jonathan Strober, Marcia Willing, Bradley L Schlaggar, Yvonne W Wu,[...]. Pediatr Neurol 2016
46
57

De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy.
Kazuyuki Nakamura, Hirofumi Kodera, Tenpei Akita, Masaaki Shiina, Mitsuhiro Kato, Hideki Hoshino, Hiroshi Terashima, Hitoshi Osaka, Shinichi Nakamura, Jun Tohyama,[...]. Am J Hum Genet 2013
118
57

Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of Literature.
David C Schorling, Tobias Dietel, Christina Evers, Katrin Hinderhofer, Rudolf Korinthenberg, Daniel Ezzo, Carsten G Bönnemann, Janbernd Kirschner. Neuropediatrics 2017
18
42

GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS.
Michaela Waak, Shekeeb S Mohammad, David Coman, Kate Sinclair, Lisa Copeland, Peter Silburn, Terry Coyne, Jim McGill, Mary O'Regan, Richard Selway,[...]. J Neurol Neurosurg Psychiatry 2018
30
42

Recurrent GNAO1 Mutations Associated With Developmental Delay and a Movement Disorder.
Leonie A Menke, Marc Engelen, Mariel Alders, Vincent J J Odekerken, Frank Baas, Jan M Cobben. J Child Neurol 2016
24
42

Progressive Movement Disorder in Brothers Carrying a GNAO1 Mutation Responsive to Deep Brain Stimulation.
Neil Kulkarni, Sha Tang, Ratan Bhardwaj, Saunder Bernes, Theresa A Grebe. J Child Neurol 2016
40
42

GNAO1-associated epileptic encephalopathy and movement disorders: c.607G>A variant represents a probable mutation hotspot with a distinct phenotype.
Ravindra Arya, Christine Spaeth, Donald L Gilbert, James L Leach, Katherine D Holland. Epileptic Disord 2017
17
35

Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review.
Tommaso Schirinzi, Giacomo Garone, Lorena Travaglini, Gessica Vasco, Serena Galosi, Loreto Rios, Claudia Castiglioni, Claudia Barassi, Domenica Battaglia, Maria Luigia Gambardella,[...]. Parkinsonism Relat Disord 2019
19
35

Excellent response to deep brain stimulation in a young girl with GNAO1-related progressive choreoathetosis.
Sanem Yilmaz, Tuncer Turhan, Serdar Ceylaner, Sarenur Gökben, Hasan Tekgul, Gul Serdaroglu. Childs Nerv Syst 2016
24
28

GNAO1 encephalopathy: further delineation of a severe neurodevelopmental syndrome affecting females.
Anna Marcé-Grau, James Dalton, Javier López-Pisón, María Concepción García-Jiménez, Lorena Monge-Galindo, Ester Cuenca-León, Jesús Giraldo, Alfons Macaya. Orphanet J Rare Dis 2016
21
28

GNAO1-Associated Movement Disorder.
Radhika Dhamija, Jonathan W Mink, Binit B Shah, Howard P Goodkin. Mov Disord Clin Pract 2016
12
33

Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy.
Christine P Diggle, Stacey J Sukoff Rizzo, Michael Popiolek, Reetta Hinttala, Jan-Philip Schülke, Manju A Kurian, Ian M Carr, Alexander F Markham, David T Bonthron, Christopher Watson,[...]. Am J Hum Genet 2016
40
28

Multiple neurological abnormalities in mice deficient in the G protein Go.
M Jiang, M S Gold, G Boulay, K Spicher, M Peyton, P Brabet, Y Srinivasan, U Rudolph, G Ellison, L Birnbaumer. Proc Natl Acad Sci U S A 1998
162
28

Clinical Phenotype of De Novo GNAO1 Mutation: Case Report and Review of Literature.
Inga Talvik, Rikke S Møller, Merilin Vaher, Ulvi Vaher, Line Hg Larsen, Hans A Dahl, Pilvi Ilves, Tiina Talvik. Child Neurol Open 2015
17
21

A case of severe movement disorder with GNAO1 mutation responsive to topiramate.
Saori Sakamoto, Yukifumi Monden, Ryoko Fukai, Noriko Miyake, Hiroshi Saito, Akihiko Miyauchi, Ayumi Matsumoto, Masako Nagashima, Hitoshi Osaka, Naomichi Matsumoto,[...]. Brain Dev 2017
15
21

PEHO Syndrome May Represent Phenotypic Expansion at the Severe End of the Early-Onset Encephalopathies.
Pawel Gawlinski, Renata Posmyk, Tomasz Gambin, Danuta Sielicka, Monika Chorazy, Beata Nowakowska, Shalini N Jhangiani, Donna M Muzny, Monika Bekiesinska-Figatowska, Jerzy Bal,[...]. Pediatr Neurol 2016
19
21

Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
Xiaolin Zhu, Slavé Petrovski, Pingxing Xie, Elizabeth K Ruzzo, Yi-Fan Lu, K Melodi McSweeney, Bruria Ben-Zeev, Andreea Nissenkorn, Yair Anikster, Danit Oz-Levi,[...]. Genet Med 2015
191
21


Molecular mechanisms of go signaling.
Meisheng Jiang, Neil S Bajpayee. Neurosignals 2009
65
21

Deep brain stimulation is effective in pediatric patients with GNAO1 associated severe hyperkinesia.
Anne Koy, Sebahattin Cirak, Victoria Gonzalez, Kerstin Becker, Thomas Roujeau, Christophe Milesi, Julien Baleine, Gilles Cambonie, Alain Boularan, Frederic Greco,[...]. J Neurol Sci 2018
22
21

ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.
Miryam Carecchio, Niccolò E Mencacci, Alessandro Iodice, Roser Pons, Celeste Panteghini, Giovanna Zorzi, Federica Zibordi, Anastasios Bonakis, Argyris Dinopoulos, Joseph Jankovic,[...]. Parkinsonism Relat Disord 2017
42
21

Phenotypic insights into ADCY5-associated disease.
Florence C F Chang, Ana Westenberger, Russell C Dale, Martin Smith, Hardev S Pall, Belen Perez-Dueñas, Padraic Grattan-Smith, Robert A Ouvrier, Neil Mahant, Bernadette C Hanna,[...]. Mov Disord 2016
70
21

Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region.
McKenna Kelly, Meredith Park, Ivana Mihalek, Anne Rochtus, Marie Gramm, Eduardo Pérez-Palma, Erika Takle Axeen, Christina Y Hung, Heather Olson, Lindsay Swanson,[...]. Epilepsia 2019
17
21

A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary chorea.
Vincenzo Salpietro, Belen Perez-Dueñas, Kosuke Nakashima, Victoria San Antonio-Arce, Andreea Manole, Stephanie Efthymiou, Jana Vandrovcova, Conceicao Bettencourt, Niccolò E Mencacci, Christine Klein,[...]. Mov Disord 2018
23
21


PDE10A and ADCY5 mutations linked to molecular and microstructural basal ganglia pathology.
Flavia Niccolini, Niccolo E Mencacci, Tayyabah Yousaf, Eugenii A Rabiner, Vincenzo Salpietro, Gennaro Pagano, Bettina Balint, Stephanie Efthymiou, Henry Houlden, Roger N Gunn,[...]. Mov Disord 2018
17
21

Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia.
Ying-Zhang Chen, Jennifer R Friedman, Dong-Hui Chen, Guy C-K Chan, Cinnamon S Bloss, Fuki M Hisama, Sarah E Topol, Andrew R Carson, Phillip H Pham, Emily S Bonkowski,[...]. Ann Neurol 2014
76
21

De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions.
Niccolò E Mencacci, Erik-Jan Kamsteeg, Kosuke Nakashima, Lea R'Bibo, David S Lynch, Bettina Balint, Michèl A A P Willemsen, Matthew E Adams, Sarah Wiethoff, Kazunori Suzuki,[...]. Am J Hum Genet 2016
62
21

ADCY5 mutations are another cause of benign hereditary chorea.
Niccolo E Mencacci, Roberto Erro, Sarah Wiethoff, Joshua Hersheson, Mina Ryten, Bettina Balint, Christos Ganos, Maria Stamelou, Niall Quinn, Henry Houlden,[...]. Neurology 2015
50
21

Mouse models of GNAO1-associated movement disorder: Allele- and sex-specific differences in phenotypes.
Huijie Feng, Casandra L Larrivee, Elena Y Demireva, Huirong Xie, Jeff R Leipprandt, Richard R Neubig. PLoS One 2019
7
42

Emerging Monogenic Complex Hyperkinetic Disorders.
Miryam Carecchio, Niccolò E Mencacci. Curr Neurol Neurosci Rep 2017
31
14

Genomic analysis identifies masqueraders of full-term cerebral palsy.
Yusuke Takezawa, Atsuo Kikuchi, Kazuhiro Haginoya, Tetsuya Niihori, Yurika Numata-Uematsu, Takehiko Inui, Saeko Yamamura-Suzuki, Takuya Miyabayashi, Mai Anzai, Sato Suzuki-Muromoto,[...]. Ann Clin Transl Neurol 2018
37
14

Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy.
Chun-Yiu Law, Sharon Tzu-Lun Chang, Sun Young Cho, Eric Kin-Cheong Yau, Grace Sui-Fun Ng, Nai-Chung Fong, Ching-Wan Lam. Clin Chim Acta 2015
23
14

GNAO1 Mutation-Induced Pediatric Dystonic Storm Rescue With Pallidal Deep Brain Stimulation.
C Michael Honey, Armaan K Malhotra, Maja Tarailo-Graovac, Clara D M van Karnebeek, Gabriella Horvath, Adi Sulistyanto. J Child Neurol 2018
10
20

Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing.
Theodora U J Bruun, Caro-Lyne DesRoches, Diane Wilson, Vann Chau, Tadashi Nakagawa, Masahiro Yamasaki, Shinya Hasegawa, Toshiyuki Fukao, Christian Marshall, Saadet Mercimek-Andrews. Genet Med 2018
22
14

Gαo (GNAO1) encephalopathies: plasma membrane vs. Golgi functions.
Gonzalo P Solis, Vladimir L Katanaev. Oncotarget 2017
6
33


Regulator of G protein signaling protein suppression of Galphao protein-mediated alpha2A adrenergic receptor inhibition of mouse hippocampal CA3 epileptiform activity.
Brianna L Goldenstein, Brian W Nelson, Ke Xu, Elizabeth J Luger, Jacquline A Pribula, Jenna M Wald, Lorraine A O'Shea, David Weinshenker, Raelene A Charbeneau, Xinyan Huang,[...]. Mol Pharmacol 2009
24
14

Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.
Michèl A Willemsen, Marcel M Verbeek, Erik-Jan Kamsteeg, Johanneke F de Rijk-van Andel, Alec Aeby, Nenad Blau, Alberto Burlina, Maria A Donati, Ben Geurtz, Padraic J Grattan-Smith,[...]. Brain 2010
115
14


Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series.
Marisela E Dy, Florence C F Chang, Sol De Jesus, Irina Anselm, Neil Mahant, Pamela Zeilman, Lance H Rodan, Kelly D Foote, Wen-Hann Tan, Emad Eskandar,[...]. J Child Neurol 2016
26
14

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
Arvid Suls, Peter Dedeken, Karolien Goffin, Hilde Van Esch, Patrick Dupont, David Cassiman, Judith Kempfle, Thomas V Wuttke, Yvonne Weber, Holger Lerche,[...]. Brain 2008
207
14

Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder.
Noa Lipstein, Nanda M Verhoeven-Duif, Francesco E Michelassi, Nathaniel Calloway, Peter M van Hasselt, Katarzyna Pienkowska, Gijs van Haaften, Mieke M van Haelst, Ron van Empelen, Inge Cuppen,[...]. J Clin Invest 2017
50
14

The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Alice R Gardiner, Fatima Jaffer, Russell C Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, Maria Stamelou, Matthew Walker, Dimitri Kullmann,[...]. Brain 2015
78
14

Beyond dystonia and ataxia: Expanding the phenotype of SQSTM1 mutations.
Carlos Zúñiga-Ramírez, Lais Machado de Oliveira, Mirelle Kramis-Hollands, Musleh Algarni, Alberto Soto-Escageda, Michel Sáenz-Farret, Héctor Alberto González-Usigli, Alfonso Fasano. Parkinsonism Relat Disord 2019
7
28

Triheptanoin dramatically reduces paroxysmal motor disorder in patients with GLUT1 deficiency.
Fanny Mochel, Elodie Hainque, Domitille Gras, Isaac M Adanyeguh, Samantha Caillet, Bénédicte Héron, Agathe Roubertie, Elsa Kaphan, Romain Valabregue, Daisy Rinaldi,[...]. J Neurol Neurosurg Psychiatry 2016
55
14

The spectrum of movement disorders in Glut-1 deficiency.
Roser Pons, Abbie Collins, Michael Rotstein, Kristin Engelstad, Darryl C De Vivo. Mov Disord 2010
94
14


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.