A citation-based method for searching scientific literature

Matthew Jensen, R Frank Kooy, Tony J Simon, Edwin Reyniers, Santhosh Girirajan, Flora Tassone. Eur J Med Genet 2018
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
381
30

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
398
30

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.
Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, Jonathan H Chung, Hiroko Nomaru, Christopher L Campbell, Anna Blonska, Anne S Bassett, Eva W C Chow, Elisabeth E Mlynarski,[...]. Circ Cardiovasc Genet 2017
13
20

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
920
20

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
20

Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update.
B De Smedt, K Devriendt, J-P Fryns, A Vogels, M Gewillig, A Swillen. J Intellect Disabil Res 2007
101
20

Cognitive development in children with 22q11.2 deletion syndrome.
Sasja N Duijff, Petra W J Klaassen, Henriette F N Swanenburg de Veye, Frits A Beemer, Gerben Sinnema, Jacob A S Vorstman. Br J Psychiatry 2012
63
20

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.
M Woodin, P P Wang, D Aleman, D McDonald-McGinn, E Zackai, E Moss. Genet Med 2001
175
20

A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.
Stephen R Hooper, Kathleen Curtiss, Kelly Schoch, Matcheri S Keshavan, Andrew Allen, Vandana Shashi. Res Dev Disabil 2013
38
20

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
E M Moss, M L Batshaw, C B Solot, M Gerdes, D M McDonald-McGinn, D A Driscoll, B S Emanuel, E H Zackai, P P Wang. J Pediatr 1999
217
20

Genotype-phenotype correlation in 22q11.2 deletion syndrome.
Elena Michaelovsky, Amos Frisch, Miri Carmel, Miriam Patya, Omer Zarchi, Tamar Green, Lina Basel-Vanagaite, Abraham Weizman, Doron Gothelf. BMC Med Genet 2012
62
20

Cognition, psychosocial adjustment and coping in familial cases of velocardiofacial syndrome.
D Gothelf, A Aviram-Goldring, M Burg, T Steinberg, M Mahajnah, A Frisch, S Fennig, G Zalsman, A Weizman. J Neural Transm (Vienna) 2007
5
40

Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion.
Petra Klaassen, Sasja Duijff, Henriëtte Swanenburg de Veye, Frits Beemer, Gerben Sinnema, Elemi Breetvelt, Renske Schappin, Jacob Vorstman. Am J Med Genet B Neuropsychiatr Genet 2016
17
20

High rate of disease-related copy number variations in childhood onset schizophrenia.
K Ahn, N Gotay, T M Andersen, A A Anvari, P Gochman, Y Lee, S Sanders, S Guha, A Darvasi, J T Glessner,[...]. Mol Psychiatry 2014
78
20

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
20

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.
Itaru Kushima, Branko Aleksic, Masahiro Nakatochi, Teppei Shimamura, Takashi Okada, Yota Uno, Mako Morikawa, Kanako Ishizuka, Tomoko Shiino, Hiroki Kimura,[...]. Cell Rep 2018
77
20

High-resolution copy number variation analysis of schizophrenia in Japan.
I Kushima, B Aleksic, M Nakatochi, T Shimamura, T Shiino, A Yoshimi, H Kimura, Y Takasaki, C Wang, J Xing,[...]. Mol Psychiatry 2017
54
20

Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders.
Christopher B Eaton, Rhys H Thomas, Khalid Hamandi, Gareth C Payne, Michael P Kerr, David E J Linden, Michael J Owen, Adam C Cunningham, Ullrich Bartsch, Siske S Struik,[...]. Epilepsia 2019
13
20

Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
20

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A Rosenfeld, Katrin Mannik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cedric Le Caignec, Anke Van Dijck,[...]. Genet Med 2019
53
20

Association of Rare Copy Number Variants With Risk of Depression.
Kimberley Marie Kendall, Elliott Rees, Matthew Bracher-Smith, Sophie Legge, Lucy Riglin, Stanley Zammit, Michael Conlon O'Donovan, Michael John Owen, Ian Jones, George Kirov,[...]. JAMA Psychiatry 2019
24
20

Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.
Christa Lese Martin, Karen E Wain, Matthew T Oetjens, Kasia Tolwinski, Emily Palen, Abby Hare-Harris, Lukas Habegger, Evan K Maxwell, Jeffrey G Reid, Lauren Kasparson Walsh,[...]. JAMA Psychiatry 2020
11
20

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
20

High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
736
20

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.
Karen Crawford, Matthew Bracher-Smith, David Owen, Kimberley M Kendall, Elliott Rees, Antonio F Pardiñas, Mark Einon, Valentina Escott-Price, James T R Walters, Michael C O'Donovan,[...]. J Med Genet 2019
38
20

Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.
Wolfram Demaerel, Matthew S Hestand, Elfi Vergaelen, Ann Swillen, Marcos López-Sánchez, Luis A Pérez-Jurado, Donna M McDonald-McGinn, Elaine Zackai, Beverly S Emanuel, Bernice E Morrow,[...]. Am J Hum Genet 2017
5
20

Microdeletion and microduplication syndromes.
Anja Weise, Kristin Mrasek, Elisabeth Klein, Milene Mulatinho, Juan C Llerena, David Hardekopf, Sona Pekova, Samarth Bhatt, Nadezda Kosyakova, Thomas Liehr. J Histochem Cytochem 2012
78
10

Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis.
S S Bhatt, M Manvelyan, K Moradkhani, F Hunstig, K Mrasek, J Puechberty, G Lefort, P Sarda, A Weise, T Liehr,[...]. Cytogenet Genome Res 2014
6
16

A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.
Ina Fickelscher, Heike Starke, Eberhard Schulze, Günther Ernst, Nadezda Kosyakova, Hasmik Mkrtchyan, Kay MacDermont, Neil Sebire, Thomas Liehr. Prenat Diagn 2007
28
10

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
10

Reassessing the Evolutionary History of the 17q21 Inversion Polymorphism.
Joao M Alves, Ana C Lima, Isa A Pais, Nadir Amir, Ricardo Celestino, Giovanna Piras, Maria Monne, David Comas, Peter Heutink, Lounès Chikhi,[...]. Genome Biol Evol 2015
3
33

The human genome puzzle - the role of copy number variation in somatic mosaicism.
Hasmik Mkrtchyan, Madeleine Gross, Sophie Hinreiner, Anna Polytiko, Marina Manvelyan, Kristin Mrasek, Nadezda Kosyakova, Elisabeth Ewers, Heike Nelle, Thomas Liehr,[...]. Curr Genomics 2010
30
10

Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion.
T Liehr, B Rautenstrauss, H Grehl, K D Bathke, A Ekici, A Rauch, H D Rott. Hum Genet 1996
37
10

Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.
Yukiko Kuroda, Ikuko Ohashi, Toshiyuki Saito, Jun-Ichi Nagai, Kazumi Ida, Takuya Naruto, Takahito Wada, Kenji Kurosawa. Am J Med Genet A 2014
5
20

Charcot-Marie-Tooth disease and related inherited neuropathies.
T Murakami, C A Garcia, L T Reiter, J R Lupski. Medicine (Baltimore) 1996
63
10

Demystifying chromosome preparation and the implications for the concept of chromosome condensation during mitosis.
U Claussen, S Michel, P Mühlig, M Westermann, U-W Grummt, K Kromeyer-Hauschild, T Liehr. Cytogenet Genome Res 2002
64
10

POD-FISH: a new technique for parental origin determination based on copy number variation polymorphism.
Anja Weise, Madeleine Gross, Sophie Hinreiner, Vera Witthuhn, Hasmik Mkrtchyan, Thomas Liehr. Methods Mol Biol 2010
8
12


Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions.
Giorgio Gimelli, Miguel Angel Pujana, Maria Grazia Patricelli, Silvia Russo, Daniela Giardino, Lidia Larizza, Joseph Cheung, Lluís Armengol, Albert Schinzel, Xavier Estivill,[...]. Hum Mol Genet 2003
94
10


Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio.
Jason C Ting, Elisha D O Roberson, Nathaniel D Miller, Alana Lysholm-Bernacchi, Dietrich A Stephan, George T Capone, Ingo Ruczinski, George H Thomas, Jonathan Pevsner. Hum Mutat 2007
36
10

Mechanisms for recurrent and complex human genomic rearrangements.
Pengfei Liu, Claudia M B Carvalho, P J Hastings, James R Lupski. Curr Opin Genet Dev 2012
214
10


Meiotic segregation of translocations during male gametogenesis.
Frédéric Morel, Nathalie Douet-Guilbert, Marie-Josée Le Bris, Angèle Herry, Véronique Amice, Jean Amice, Marc De Braekeleer. Int J Androl 2004
57
10

Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects.
James R Priest, Santhosh Girirajan, Tiffany H Vu, Aaron Olson, Evan E Eichler, Michael A Portman. Am J Med Genet A 2012
30
10

Replication stress and mechanisms of CNV formation.
Martin F Arlt, Thomas E Wilson, Thomas W Glover. Curr Opin Genet Dev 2012
62
10

The use of array-CGH in a cohort of Greek children with developmental delay.
Emmanouil Manolakos, Annalisa Vetro, Konstantinos Kefalas, Stamatia-Maria Rapti, Eirini Louizou, Antonios Garas, George Kitsos, Lefteris Vasileiadis, Panagiota Tsoplou, Makarios Eleftheriades,[...]. Mol Cytogenet 2010
19
10

Sex ratios in fetuses and liveborn infants with autosomal aneuploidy.
C A Huether, R L Martin, S M Stoppelman, S D'Souza, J K Bishop, C P Torfs, F Lorey, K M May, J S Hanna, P A Baird,[...]. Am J Med Genet 1996
43
10

Cytogenetic studies in male infertility: a review.
M De Braekeleer, T N Dao. Hum Reprod 1991
282
10

Detailed analysis of inversions predicted between two human genomes: errors, real polymorphisms, and their origin and population distribution.
David Vicente-Salvador, Marta Puig, Magdalena Gayà-Vidal, Sarai Pacheco, Carla Giner-Delgado, Isaac Noguera, David Izquierdo, Alexander Martínez-Fundichely, Aurora Ruiz-Herrera, Xavier Estivill,[...]. Hum Mol Genet 2017
6
16


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.