A citation-based method for searching scientific literature

Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren, Bhooma Thiruvahindrapduram, Andreas Fiebig, Stefan Schreiber, Jan Friedman, Cees E J Ketelaars, Yvonne J Vos, Can Ficicioglu, Susan Kirkpatrick, Rob Nicolson, Leon Sloman, Anne Summers, Clare A Gibbons, Ahmad Teebi, David Chitayat, Rosanna Weksberg, Ann Thompson, Cathy Vardy, Vicki Crosbie, Sandra Luscombe, Rebecca Baatjes, Lonnie Zwaigenbaum, Wendy Roberts, Bridget Fernandez, Peter Szatmari, Stephen W Scherer. Am J Hum Genet 2008
Times Cited: 1170







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



Times Cited
  Times     Co-cited
Similarity


Morphological differences in the mirror neuron system in Williams syndrome.
Rowena Ng, Timothy T Brown, Matthew Erhart, Anna M Järvinen, Julie R Korenberg, Ursula Bellugi, Eric Halgren. Soc Neurosci 2016
4
25

Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): a cross-sectional and longitudinal study.
Marie Schaer, Martin Debbané, Meritxell Bach Cuadra, Marie-Christine Ottet, Bronwyn Glaser, Jean-Philippe Thiran, Stephan Eliez. Schizophr Res 2009
81
1


Performance on the Kaufman Brief Intelligence Test-2 by Children With Williams Syndrome.
C Holley Pitts, Carolyn B Mervis. Am J Intellect Dev Disabil 2016
6
16

Deficits in voice and multisensory processing in patients with Prader-Willi syndrome.
Juliette Salles, Kuzma Strelnikov, Mantoulan Carine, Thuilleaux Denise, Virginie Laurier, Catherine Molinas, Maïthé Tauber, Pascal Barone. Neuropsychologia 2016
7
14

Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.
T van Amelsvoort, J Zinkstok, M Figee, E Daly, R Morris, M J Owen, K C Murphy, L De Haan, D H Linszen, B Glaser,[...]. Psychol Med 2008
38
2


Abnormalities in gray matter microstructure in young adults with 22q11.2 deletion syndrome.
Zora Kikinis, Nikos Makris, Valerie J Sydnor, Sylvain Bouix, Ofer Pasternak, Ioana L Coman, Kevin M Antshel, Wanda Fremont, Marek R Kubicki, Martha E Shenton,[...]. Neuroimage Clin 2019
3
33

The relationship between compulsive behaviour and academic achievement across the three genetic subtypes of Prader-Willi syndrome.
J Zarcone, D Napolitano, C Peterson, J Breidbord, S Ferraioli, M Caruso-Anderson, L Holsen, M G Butler, T Thompson. J Intellect Disabil Res 2007
40
2

Facial emotion processing in patients with social anxiety disorder and Williams-Beuren syndrome: an fMRI study.
Cynthia Binelli, Armando Muñiz, Susana Subira, Ricard Navines, Laura Blanco-Hinojo, Debora Perez-Garcia, Jose Crippa, Magi Farré, Luis Pérez-Jurado, Jesus Pujol,[...]. J Psychiatry Neurosci 2016
9
11

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
174
1

Clinical implications of copy number variations in autoimmune disorders.
Seon-Hee Yim, Seung-Hyun Jung, Boram Chung, Yeun-Jun Chung. Korean J Intern Med 2015
8
12

Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults.
K Momma, A Takao, R Matsuoka, Y Imai, A Muto, M Osawa, M Takayama. Genet Med 2001
18
5

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome.
J Whittington, A Holland, T Webb, J Butler, D Clarke, H Boer. J Intellect Disabil Res 2004
104
1

3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.
Ming-Chang Chiang, Allan L Reiss, Agatha D Lee, Ursula Bellugi, Albert M Galaburda, Julie R Korenberg, Debra L Mills, Arthur W Toga, Paul M Thompson. Neuroimage 2007
106
1

Copy Number Variation Disorders.
Tamim H Shaikh. Curr Genet Med Rep 2017
10
10

Childhood Executive Functioning Predicts Young Adult Outcomes in 22q11.2 Deletion Syndrome.
Avery B Albert, Tamara Abu-Ramadan, Wendy R Kates, Wanda Fremont, Kevin M Antshel. J Int Neuropsychol Soc 2018
3
33


Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome.
Adam C Cunningham, Sue Delport, Wendy Cumines, Monica Busse, David E J Linden, Jeremy Hall, Michael J Owen, Marianne B M van den Bree. Br J Psychiatry 2018
12
8

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
36
2

A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome.
Melanie A Porter, Carol Dobson-Stone, John B J Kwok, Peter R Schofield, William Beckett, May Tassabehji. PLoS One 2012
24
4

Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects.
Miri Carmel, Omer Zarchi, Elena Michaelovsky, Amos Frisch, Miriam Patya, Tamar Green, Doron Gothelf, Abraham Weizman. J Psychiatr Res 2014
13
7

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
216
1

Lateral preference in Williams-Beuren syndrome is associated with cognition and language.
D Pérez-García, R Flores, C Brun-Gasca, L A Pérez-Jurado. Eur Child Adolesc Psychiatry 2015
6
16

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.
E Hidding, H Swaab, L M J de Sonneville, H van Engeland, J A S Vorstman. Clin Genet 2016
10
10

Abilities and attainment in Smith-Magenis syndrome.
O Udwin, C Webber, I Horn. Dev Med Child Neurol 2001
32
3

Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish.
Sandra C Doelken, Sebastian Köhler, Christopher J Mungall, Georgios V Gkoutos, Barbara J Ruef, Cynthia Smith, Damian Smedley, Sebastian Bauer, Eva Klopocki, Paul N Schofield,[...]. Dis Model Mech 2013
32
3


Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndrome.
A Vangkilde, J R M Jepsen, H Schmock, C Olesen, S Arnarsdóttir, W F C Baaré, K J Plessen, M Didriksen, H R Siebner, T Werge,[...]. J Neurodev Disord 2016
17
5

Increased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sample.
Guia Guffanti, Federica Torri, Jerod Rasmussen, Andrew P Clark, Anita Lakatos, Jessica A Turner, James H Fallon, Andrew J Saykin, Michael Weiner, Marquis P Vawter,[...]. Genomics 2013
19
5

22q11.2 deletion syndrome: are motor deficits more than expected for IQ level?
Nancy J Roizen, Anne M Higgins, Kevin M Antshel, Wanda Fremont, Robert Shprintzen, Wendy R Kates. J Pediatr 2010
16
6

A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.
O Zarchi, A Diamond, R Weinberger, D Abbott, M Carmel, A Frisch, E Michaelovsky, R Gruber, T Green, A Weizman,[...]. Eur Psychiatry 2014
18
5

IQ and hemizygosity for the Val158 Met functional polymorphism of COMT in 22q11DS.
Colleen P Franconi, Donna McDonald-McGinn, Elaine H Zackai, Meghan A McNamara, Harold Salmons, Edward Moss, Raquel E Gur, Marcella Devoto, Beverly S Emanuel. Am J Med Genet B Neuropsychiatr Genet 2016
3
33

Effect of cessation of GH treatment on cognition during transition phase in Prader-Willi syndrome: results of a 2-year crossover GH trial.
R J Kuppens, E F Mahabier, N E Bakker, E P C Siemensma, S H Donze, A C S Hokken-Koelega. Orphanet J Rare Dis 2016
10
10

Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study.
Daniel S Tylee, Zora Kikinis, Thomas P Quinn, Kevin M Antshel, Wanda Fremont, Muhammad A Tahir, Anni Zhu, Xue Gong, Stephen J Glatt, Ioana L Coman,[...]. Neuroimage Clin 2017
15
6

Acceptability and Reliability of the Bayley Scales of Infant and Toddler Development-III Among Children in Bhaktapur, Nepal.
Suman Ranjitkar, Ingrid Kvestad, Tor A Strand, Manjeswori Ulak, Merina Shrestha, Ram K Chandyo, Laxman Shrestha, Mari Hysing. Front Psychol 2018
15
6

Mental health problems in children with prader-willi syndrome.
Norbert Skokauskas, Eileen Sweeny, Judith Meehan, Louise Gallagher. J Can Acad Child Adolesc Psychiatry 2012
24
4

Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome.
Tracy Yuen, Eva W C Chow, Candice K Silversides, Anne S Bassett. Schizophr Res 2013
18
5

Ammons quick test validity among randomly selected referrals.
Robert John Zagar, Joseph W Kovach, Kenneth G Busch, Michael D Zablocki, William Osnowitz, Jonas Neuhengen, Yutong Liu, Agata Karolina Zagar. Psychol Rep 2013
7
14

Childhood cognitive development in 22q11.2 deletion syndrome: case-control study.
Samuel J R A Chawner, Joanne L Doherty, Hayley Moss, Maria Niarchou, James T R Walters, Michael J Owen, Marianne B M van den Bree. Br J Psychiatry 2017
21
4

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
61
1

Default mode network connectivity and reciprocal social behavior in 22q11.2 deletion syndrome.
Matthew J Schreiner, Katherine H Karlsgodt, Lucina Q Uddin, Carolyn Chow, Eliza Congdon, Maria Jalbrzikowski, Carrie E Bearden. Soc Cogn Affect Neurosci 2014
47
2

Expressive and receptive language in Prader-Willi syndrome: report on genetic subtype differences.
Anastasia Dimitropoulos, Angela Ferranti, Maria Lemler. J Commun Disord 2013
15
6

The effect of intellectual ability on functional activation in a neurodevelopmental disorder: preliminary evidence from multiple fMRI studies in Williams syndrome.
Jennifer R Pryweller, Suzanne N Avery, Jennifer U Blackford, Elisabeth M Dykens, Tricia A Thornton-Wells. J Neurodev Disord 2012
4
25

Anthropometric and intellectual evaluation of individuals with Prader-Willi syndrome.
San-Ging Shu, Shu Chien, Yen-Ching Wu, Pei-Ling Tsai, Joung-Kun Yih. J Formos Med Assoc 2007
6
16

Convergent evolution in the genomics era: new insights and directions.
Timothy B Sackton, Nathan Clark. Philos Trans R Soc Lond B Biol Sci 2019
15
6

Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCR.
Vicki J Hwang, Dianna Maar, John Regan, Kathleen Angkustsiri, Tony J Simon, Flora Tassone. BMC Med Genet 2014
18
5

The social brain network in 22q11.2 deletion syndrome: a diffusion tensor imaging study.
Amy K Olszewski, Zora Kikinis, Christie S Gonzalez, Ioana L Coman, Nikolaos Makris, Xue Gong, Yogesh Rathi, Anni Zhu, Kevin M Antshel, Wanda Fremont,[...]. Behav Brain Funct 2017
13
7

Diagnoses and characteristics of autism spectrum disorders in children with Prader-Willi syndrome.
Elisabeth M Dykens, Elizabeth Roof, Hailee Hunt-Hawkins, Nathan Dankner, Evon Batey Lee, Carolyn M Shivers, Christopher Daniell, Soo-Jeong Kim. J Neurodev Disord 2017
27
3

Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications.
Martin Debbané, Bronwyn Glaser, Melissa K David, Carl Feinstein, Stephan Eliez. Schizophr Res 2006
103
1


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.