A citation-based method for searching scientific literature

D Cristopher Bragg, Kotchaphorn Mangkalaphiban, Christine A Vaine, Nichita J Kulkarni, David Shin, Rachita Yadav, Jyotsna Dhakal, Mai-Linh Ton, Anne Cheng, Christopher T Russo, Mark Ang, Patrick Acuña, Criscely Go, Taylor N Franceour, Trisha Multhaupt-Buell, Naoto Ito, Ulrich Müller, William T Hendriks, Xandra O Breakefield, Nutan Sharma, Laurie J Ozelius. Proc Natl Acad Sci U S A 2017
Times Cited: 73







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



Times Cited
  Times     Co-cited
Similarity


Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly.
Tatsiana Aneichyk, William T Hendriks, Rachita Yadav, David Shin, Dadi Gao, Christine A Vaine, Ryan L Collins, Aloysius Domingo, Benjamin Currall, Alexei Stortchevoi,[...]. Cell 2018
103
61

Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism.
Satoshi Makino, Ryuji Kaji, Satoshi Ando, Maiko Tomizawa, Katsuhito Yasuno, Satoshi Goto, Shinnichi Matsumoto, Maria Daisy Tabuena, Elma Maranon, Marita Dantes,[...]. Am J Hum Genet 2007
154
52

A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism.
Ana Westenberger, Charles Jourdan Reyes, Gerard Saranza, Valerija Dobricic, Henrike Hanssen, Aloysius Domingo, Björn-Hergen Laabs, Susen Schaake, Jelena Pozojevic, Aleksandar Rakovic,[...]. Ann Neurol 2019
36
77

The unique phenomenology of sex-linked dystonia parkinsonism (XDP, DYT3, "Lubag").
Lillian V Lee, Corazon Rivera, Rosalia A Teleg, Marita B Dantes, Paul Matthew D Pasco, Roland Dominic G Jamora, Jose Arancillo, Rodelyn F Villareal-Jordan, Raymond L Rosales, Cynthia Demaisip,[...]. Int J Neurosci 2011
72
31

New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).
Aloysius Domingo, Ana Westenberger, Lillian V Lee, Ingrid Brænne, Tian Liu, Inga Vater, Raymond Rosales, Roland Dominic Jamora, Paul Matthew Pasco, Eva Maria Cutiongco-Dela Paz,[...]. Eur J Hum Genet 2015
49
42

Functional anatomy of the basal ganglia in X-linked recessive dystonia-parkinsonism.
Satoshi Goto, Lillian V Lee, Edwin L Munoz, Ikuo Tooyama, Gen Tamiya, Satoshi Makino, Satoshi Ando, Marita B Dantes, Kazumichi Yamada, Sadayuki Matsumoto,[...]. Ann Neurol 2005
120
24

Genome editing in induced pluripotent stem cells rescues TAF1 levels in X-linked dystonia-parkinsonism.
Aleksandar Rakovic, Aloysius Domingo, Karen Grütz, Leonora Kulikovskaja, Philipp Capetian, Sally A Cowley, Insa Lenz, Norbert Brüggemann, Raymond Rosales, Dominic Jamora,[...]. Mov Disord 2018
19
89

Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism.
Dagmar Nolte, Stephan Niemann, Ulrich Müller. Proc Natl Acad Sci U S A 2003
78
21

Decreased N-TAF1 expression in X-linked dystonia-parkinsonism patient-specific neural stem cells.
Naoto Ito, William T Hendriks, Jyotsna Dhakal, Christine A Vaine, Christina Liu, David Shin, Kyle Shin, Noriko Wakabayashi-Ito, Marisela Dy, Trisha Multhaupt-Buell,[...]. Dis Model Mech 2016
24
62

Basal ganglia and cerebellar pathology in X-linked dystonia-parkinsonism.
Henrike Hanssen, Marcus Heldmann, Jannik Prasuhn, Volker Tronnier, Dirk Rasche, Cid C Diesta, Aloysius Domingo, Raymond L Rosales, Roland D Jamora, Christine Klein,[...]. Brain 2018
25
60

Roles for retrotransposon insertions in human disease.
Dustin C Hancks, Haig H Kazazian. Mob DNA 2016
312
19

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations.
Jason A O'Rawe, Yiyang Wu, Max J Dörfel, Alan F Rope, P Y Billie Au, Jillian S Parboosingh, Sungjin Moon, Maria Kousi, Konstantina Kosma, Christopher S Smith,[...]. Am J Hum Genet 2015
71
18

The natural history of sex-linked recessive dystonia parkinsonism of Panay, Philippines (XDP).
Lillian V Lee, Elma Maranon, Cynthia Demaisip, Olivia Peralta, Ruth Borres-Icasiano, Jose Arancillo, Corazon Rivera, Edwin Munoz, Kenneth Tan, Marita T Reyes. Parkinsonism Relat Disord 2002
65
20

Defects in the striatal neuropeptide Y system in X-linked dystonia-parkinsonism.
Satoshi Goto, Toshitaka Kawarai, Ryoma Morigaki, Shinya Okita, Hidetaka Koizumi, Shinji Nagahiro, Edwin L Munoz, Lillian V Lee, Ryuji Kaji. Brain 2013
43
27

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
16

Neuroanatomical changes extend beyond striatal atrophy in X-linked dystonia parkinsonism.
Norbert Brüggemann, Marcus Heldmann, Christine Klein, Aloysius Domingo, Dirk Rasche, Volker Tronnier, Raymond L Rosales, Roland Dominic G Jamora, Lillian V Lee, Thomas F Münte. Parkinsonism Relat Disord 2016
27
44

Evidence of TAF1 dysfunction in peripheral models of X-linked dystonia-parkinsonism.
Aloysius Domingo, David Amar, Karen Grütz, Lillian V Lee, Raymond Rosales, Norbert Brüggemann, Roland Dominic Jamora, Eva Cutiongco-Dela Paz, Arndt Rolfs, Dirk Dressler,[...]. Cell Mol Life Sci 2016
26
42

Striatal dysfunction in X-linked dystonia-parkinsonism is associated with disease progression.
N Brüggemann, R L Rosales, J L Waugh, A J Blood, A Domingo, M Heldmann, R D Jamora, A Münchau, T F Münte, L V Lee,[...]. Eur J Neurol 2017
21
52

Phenomenology of "Lubag" or X-linked dystonia-parkinsonism.
Virgilio Gerald H Evidente, Joel Advincula, Raymund Esteban, Paul Pasco, Jhoe Anthony Alfon, Filipinas F Natividad, Joven Cuanang, Amado San Luis, Katrina Gwinn-Hardy, John Hardy,[...]. Mov Disord 2002
59
18


SVA elements: a hominid-specific retroposon family.
Hui Wang, Jinchuan Xing, Deepak Grover, Dale J Hedges, Kyudong Han, Jerilyn A Walker, Mark A Batzer. J Mol Biol 2005
230
12

Increased insula-putamen connectivity in X-linked dystonia-parkinsonism.
Anne J Blood, Jeff L Waugh, Thomas F Münte, Marcus Heldmann, Aloysius Domingo, Christine Klein, Hans C Breiter, Lillian V Lee, Raymond L Rosales, Norbert Brüggemann. Neuroimage Clin 2017
16
56

An integrated map of structural variation in 2,504 human genomes.
Peter H Sudmant, Tobias Rausch, Eugene J Gardner, Robert E Handsaker, Alexej Abyzov, John Huddleston, Yan Zhang, Kai Ye, Goo Jun, Markus Hsi-Yang Fritz,[...]. Nature 2015
12

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
12

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
12

Association of Pallidal Neurostimulation and Outcome Predictors With X-linked Dystonia Parkinsonism.
Norbert Brüggemann, Aloysius Domingo, Dirk Rasche, Christian K E Moll, Raymond L Rosales, Roland Dominic G Jamora, Henrike Hanssen, Alexander Münchau, Julia Graf, Anne Weissbach,[...]. JAMA Neurol 2019
19
47

Characterisation of the potential function of SVA retrotransposons to modulate gene expression patterns.
Abigail L Savage, Vivien J Bubb, Gerome Breen, John P Quinn. BMC Evol Biol 2013
33
27

Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy.
Mariko Taniguchi-Ikeda, Kazuhiro Kobayashi, Motoi Kanagawa, Chih-chieh Yu, Kouhei Mori, Tetsuya Oda, Atsushi Kuga, Hiroki Kurahashi, Hasan O Akman, Salvatore DiMauro,[...]. Nature 2011
111
10

Hot L1s account for the bulk of retrotransposition in the human population.
Brook Brouha, Joshua Schustak, Richard M Badge, Sheila Lutz-Prigge, Alexander H Farley, John V Moran, Haig H Kazazian. Proc Natl Acad Sci U S A 2003
682
10

Retrotransposition of marked SVA elements by human L1s in cultured cells.
Dustin C Hancks, John L Goodier, Prabhat K Mandal, Ling E Cheung, Haig H Kazazian. Hum Mol Genet 2011
139
10

Long-term outcomes of pallidal deep brain stimulation in X-linked dystonia parkinsonism (XDP): Up to 84 months follow-up and review of literature.
Joshua Emmanuel E Abejero, Roland Dominic G Jamora, Theodor S Vesagas, Rosalia A Teleg, Raymond L Rosales, Joseph P Anlacan, Monserrat S Velasquez, Jose A Aguilar. Parkinsonism Relat Disord 2019
18
44

Torsion dystonia in Panay, Philippines.
L V Lee, F M Pascasio, F D Fuentes, G H Viterbo. Adv Neurol 1976
93
10

X-Linked Dystonia-Parkinsonism: recent advances.
D Cristopher Bragg, Nutan Sharma, Laurie J Ozelius. Curr Opin Neurol 2019
12
66

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
H T Orr, M Y Chung, S Banfi, T J Kwiatkowski, A Servadio, A L Beaudet, A E McCall, L A Duvick, L P Ranum, H Y Zoghbi. Nat Genet 1993
10

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.
S E Holmes, E E O'Hearn, M G McInnis, D A Gorelick-Feldman, J J Kleiderlein, C Callahan, N G Kwak, R G Ingersoll-Ashworth, M Sherr, A J Sumner,[...]. Nat Genet 1999
332
10

Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.
Andrea Cortese, Roberto Simone, Roisin Sullivan, Jana Vandrovcova, Huma Tariq, Wai Yan Yau, Jack Humphrey, Zane Jaunmuktane, Prasanth Sivakumar, James Polke,[...]. Nat Genet 2019
167
10

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.
M Mahadevan, C Tsilfidis, L Sabourin, G Shutler, C Amemiya, G Jansen, C Neville, M Narang, J Barceló, K O'Hoy. Science 1992
10

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.
Hiroyuki Ishiura, Koichiro Doi, Jun Mitsui, Jun Yoshimura, Miho Kawabe Matsukawa, Asao Fujiyama, Yasuko Toyoshima, Akiyoshi Kakita, Hitoshi Takahashi, Yutaka Suzuki,[...]. Nat Genet 2018
137
10

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
V Campuzano, L Montermini, M D Moltò, L Pianese, M Cossée, F Cavalcanti, E Monros, F Rodius, F Duclos, A Monticelli,[...]. Science 1996
10

The impact of retrotransposons on human genome evolution.
Richard Cordaux, Mark A Batzer. Nat Rev Genet 2009
993
10

An evaluation of a SVA retrotransposon in the FUS promoter as a transcriptional regulator and its association to ALS.
Abigail L Savage, Thomas P Wilm, Kejhal Khursheed, Aleksey Shatunov, Karen E Morrison, Pamela J Shaw, Christopher E Shaw, Bradley Smith, Gerome Breen, Ammar Al-Chalabi,[...]. PLoS One 2014
25
32

Imaging gradual neurodegeneration in a basal ganglia model disease.
Henrike Hanssen, Jannik Prasuhn, Marcus Heldmann, Cid C Diesta, Aloysius Domingo, Martin Göttlich, Anne J Blood, Raymond L Rosales, Roland D G Jamora, Thomas F Münte,[...]. Ann Neurol 2019
12
66

Expanding Data Collection for the MDSGene Database: X-linked Dystonia-Parkinsonism as Use Case Example.
Martje G Pauly, Marta Ruiz López, Ana Westenberger, Gerard Saranza, Norbert Brüggemann, Anne Weissbach, Raymond L Rosales, Cid C Diesta, Roland D G Jamora, Charles J Reyes,[...]. Mov Disord 2020
15
53

Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man.
H H Kazazian, C Wong, H Youssoufian, A F Scott, D G Phillips, S E Antonarakis. Nature 1988
663
9

Neuropathology of lubag (x-linked dystonia parkinsonism).
C H Waters, P L Faust, J Powers, H Vinters, C Moskowitz, T Nygaard, A L Hunt, S Fahn. Mov Disord 1993
85
9

Nonmotor features in sex-linked dystonia parkinsonism.
Roland Dominic G Jamora, Lourdes K Ledesma, Aloysius Domingo, Alvin Rae F Cenina, Lillian V Lee. Neurodegener Dis Manag 2014
17
41

A comprehensive map of mobile element insertion polymorphisms in humans.
Chip Stewart, Deniz Kural, Michael P Strömberg, Jerilyn A Walker, Miriam K Konkel, Adrian M Stütz, Alexander E Urban, Fabian Grubert, Hugo Y K Lam, Wan-Ping Lee,[...]. PLoS Genet 2011
205
9

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
T Matsuura, T Yamagata, D L Burgess, A Rasmussen, R P Grewal, K Watase, M Khajavi, A E McCall, C F Davis, L Zu,[...]. Nat Genet 2000
357
9

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.
Nozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, Shuichi Asakawa, Taro Ishiguro, Taiji Tsunemi, Makoto Takahashi, Tohru Matsuura, Kevin M Flanigan, Sawa Iwasaki,[...]. Am J Hum Genet 2009
181
9

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
C L Liquori, K Ricker, M L Moseley, J F Jacobsen, W Kress, S L Naylor, J W Day, L P Ranum. Science 2001
840
9


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.