A citation-based method for searching scientific literature

M G Butler. J Intellect Disabil Res 2017
Times Cited: 39







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



Times Cited
  Times     Co-cited
Similarity



Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Rachel Soemedi, Ian J Wilson, Jamie Bentham, Rebecca Darlay, Ana Töpf, Diana Zelenika, Catherine Cosgrove, Kerry Setchfield, Chris Thornborough, Javier Granados-Riveron,[...]. Am J Hum Genet 2012
180
7

The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling.
Hilda T H Tsang, Thomas L Edwards, Xinnan Wang, James W Connell, Rachel J Davies, Hannah J Durrington, Cahir J O'Kane, J Paul Luzio, Evan Reid. Hum Mol Genet 2009
89
7

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
389
7

The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
194
7

Structure and control of the actin regulatory WAVE complex.
Zhucheng Chen, Dominika Borek, Shae B Padrick, Timothy S Gomez, Zoltan Metlagel, Ayman M Ismail, Junko Umetani, Daniel D Billadeau, Zbyszek Otwinowski, Michael K Rosen. Nature 2010
289
7

New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.
Sabiha Abekhoukh, H Bahar Sahin, Mauro Grossi, Samantha Zongaro, Thomas Maurin, Irene Madrigal, Daniele Kazue-Sugioka, Annick Raas-Rothschild, Mohamed Doulazmi, Pilar Carrera,[...]. Dis Model Mech 2017
33
9

Fragile X spectrum disorders.
Reymundo Lozano, Carolina Alba Rosero, Randi J Hagerman. Intractable Rare Dis Res 2014
86
7

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Heather C Mefford, Andrew J Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K Maloney, John A Crolla, Diana Baralle,[...]. N Engl J Med 2008
514
7

Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Raphael Bernier, Kyle J Steinman, Beau Reilly, Arianne Stevens Wallace, Elliott H Sherr, Nicholas Pojman, Heather C Mefford, Jennifer Gerdts, Rachel Earl, Ellen Hanson,[...]. Genet Med 2016
73
7

NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.
Yuwu Jiang, Yuehua Zhang, Pingping Zhang, Tian Sang, Feng Zhang, Taoyun Ji, Qionghui Huang, Han Xie, Renqian Du, Bin Cai,[...]. Hum Genet 2012
25
12

Does variation in NIPA2 contribute to genetic generalized epilepsy?
Michael S Hildebrand, John A Damiano, Saul A Mullen, Susannah T Bellows, Ingrid E Scheffer, Samuel F Berkovic. Hum Genet 2014
6
50

Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families.
Suqin Chen, Chun Song, Hui Guo, Pingyi Xu, Weijun Huang, Yan Zhou, Jiandong Sun, Cai-Xia Li, Yong Du, Xunhua Li,[...]. Hum Mutat 2005
38
7

Clinical and genetic aspects of Angelman syndrome.
Charles A Williams, Daniel J Driscoll, Aditi I Dagli. Genet Med 2010
154
7

Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility.
Ana I Silva, Josephine E Haddon, Yasir Ahmed Syed, Simon Trent, Tzu-Ching E Lin, Yateen Patel, Jenny Carter, Niels Haan, Robert C Honey, Trevor Humby,[...]. Nat Commun 2019
24
12


Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
Anthony R Isles, Andrés Ingason, Chelsea Lowther, James Walters, Micha Gawlick, Gerald Stöber, Elliott Rees, Joanna Martin, Rosie B Little, Harry Potter,[...]. PLoS Genet 2016
32
9

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank.
Simon G Williams, Apostol Nakev, Hui Guo, Simon Frain, Gennadiy Tenin, Anna Liakhovitskaia, Priyanka Saha, James R Priest, Kathryn E Hentges, Bernard D Keavney. Eur J Hum Genet 2020
3
100

Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
Trilochan Sahoo, Carlos A Bacino, Jennifer R German, Chad A Shaw, Lynne M Bird, Virginia Kimonis, Irinia Anselm, Susan Waisbren, Arthur L Beaudet, Sarika U Peters. Eur J Hum Genet 2007
57
7

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
7

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
154
7

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
643
7

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
S L Christian, J A Fantes, S K Mewborn, B Huang, D H Ledbetter. Hum Mol Genet 1999
192
5

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.
D H Ledbetter, V M Riccardi, S D Airhart, R J Strobel, B S Keenan, J D Crawford. N Engl J Med 1981
488
5

UPD detection using homozygosity profiling with a SNP genotyping microarray.
Peter Papenhausen, Stuart Schwartz, Hiba Risheg, Elisabeth Keitges, Inder Gadi, Rachel D Burnside, Vikram Jaswaney, John Pappas, Romela Pasion, Kenneth Friedman,[...]. Am J Med Genet A 2011
86
5

Maladaptive behaviors and risk factors among the genetic subtypes of Prader-Willi syndrome.
Sigan L Hartley, William E Maclean, Merlin G Butler, Jennifer Zarcone, Travis Thompson. Am J Med Genet A 2005
68
5

Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.
Soo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, Jennifer Ruth German, Arthur L Beaudet, Trilochan Sahoo, Daniel J Driscoll. Eur J Hum Genet 2012
61
5

The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.
Nora Urraca, Julie Cleary, Victoria Brewer, Eniko K Pivnick, Kathryn McVicar, Ronald L Thibert, N Carolyn Schanen, Carmen Esmer, Dustin Lamport, Lawrence T Reiter. Autism Res 2013
90
5

Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
Louisa Kalsner, Stormy J Chamberlain. Pediatr Clin North Am 2015
48
5



Novel West syndrome candidate genes in a Chinese cohort.
Jing Peng, Ying Wang, Fang He, Chen Chen, Li-Wen Wu, Li-Fen Yang, Yu-Ping Ma, Wen Zhang, Zi-Qing Shi, Chao Chen,[...]. CNS Neurosci Ther 2018
28
7

Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.
Kihoon Han, Hogmei Chen, Vincenzo A Gennarino, Ronald Richman, Hui-Chen Lu, Huda Y Zoghbi. Hum Mol Genet 2015
41
5

Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice.
Ozlem Bozdagi, Takeshi Sakurai, Nathan Dorr, Marion Pilorge, Nagahide Takahashi, Joseph D Buxbaum. PLoS One 2012
72
5

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism.
Jennifer C Darnell, Sarah J Van Driesche, Chaolin Zhang, Ka Ying Sharon Hung, Aldo Mele, Claire E Fraser, Elizabeth F Stone, Cynthia Chen, John J Fak, Sung Wook Chi,[...]. Cell 2011
5

CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.
Annette Schenck, Barbara Bardoni, Caillin Langmann, Nicholas Harden, Jean Louis Mandel, Angela Giangrande. Neuron 2003
241
5

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.
Andrés Ingason, George Kirov, Ina Giegling, Thomas Hansen, Anthony R Isles, Klaus D Jakobsen, Kari T Kristinsson, Louise le Roux, Omar Gustafsson, Nick Craddock,[...]. Am J Psychiatry 2011
68
5

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker,[...]. Nat Genet 2010
411
5

[15Q11.2 (BP1-BP2) microdeletion, a new syndrome with variable expressivity].
A Sempere Pérez, I Manchón Trives, I Palazón Azorín, L Alcaraz Más, E Pérez Lledó, F Galán Sánchez. An Pediatr (Barc) 2011
12
16

BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications.
D P Locke, R Segraves, R D Nicholls, S Schwartz, D Pinkel, D G Albertson, E E Eichler. J Med Genet 2004
70
5

15q11.2 proximal imbalances associated with a diverse array of neuropsychiatric disorders and mild dysmorphic features.
Ahmed T Abdelmoity, Jean-Baptiste LePichon, Sarah S Nyp, Sarah E Soden, Carol A Daniel, Shihui Yu. J Dev Behav Pediatr 2012
32
6

Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies.
Johanna A Jähn, Sarah von Spiczak, Hiltrud Muhle, Tanja Obermeier, Andre Franke, Heather C Mefford, Ulrich Stephani, Ingo Helbig. Epilepsy Res 2014
15
13

Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies.
Joanna Lazier, Deborah Fruitman, Julie Lauzon, Francois Bernier, Bob Argiropoulos, Judy Chernos, Oana Caluseriu, Rebecca Simrose, Mary Ann Thomas. J Obstet Gynaecol Can 2016
8
25

Congenital Arthrogryposis: An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?
K M Usrey, C A Williams, M Dasouki, L C Fairbrother, M G Butler. Case Rep Genet 2014
10
20

Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.
M Egloff, B Hervé, T Quibel, S Jaillard, G Le Bouar, K Uguen, A-H Saliou, M Valduga, E Perdriolle, C Coutton,[...]. Ultrasound Obstet Gynecol 2018
18
11

15q11.2 microdeletion and hypoplastic left heart syndrome.
Chiara Barone, Antonio Novelli, Innocenzo Bianca, Antonella Cataliotti Del Grano, Marcello Campisi, Carla Ettore, Elisa Pappalardo, Lara Indaco, Giuseppe Ettore, Giovanni Bartoloni,[...]. Eur J Med Genet 2015
4
50


Specific effect of the fragile-X mental retardation-1 gene (FMR1) on white matter microstructure.
Tamar Green, Naama Barnea-Goraly, Mira Raman, Scott S Hall, Amy A Lightbody, Jennifer L Bruno, Eve-Marie Quintin, Allan L Reiss. Br J Psychiatry 2015
13
15

Profiles of aberrant white matter microstructure in fragile X syndrome.
Scott S Hall, Robert F Dougherty, Allan L Reiss. Neuroimage Clin 2016
14
14

CNVs in neuropsychiatric disorders.
George Kirov. Hum Mol Genet 2015
77
5


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.