A citation-based method for searching scientific literature

Oanh Kieu Vo, Alisdair McNeill, Katharina Sophie Vogt. Am J Med Genet A 2018
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan,[...]. J Pediatr 2011
299
46

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
408
38



A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
Lorenzo D Botto, Kristin May, Paul M Fernhoff, Adolfo Correa, Karlene Coleman, Sonja A Rasmussen, Robert K Merritt, Leslie A O'Leary, Lee-Yang Wong, E Marsha Elixson,[...]. Pediatrics 2003
414
30

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
274
30

22q11.2 deletion syndrome: attitudes towards disclosing the risk of psychiatric illness.
Nicole Martin, Marina Mikhaelian, Cheryl Cytrynbaum, Cheryl Shuman, David A Chitayat, Rosanna Weksberg, Anne S Bassett. J Genet Couns 2012
20
30

Perceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome.
D J Karas, G Costain, E W C Chow, A S Bassett. J Intellect Disabil Res 2014
12
33

Practical guidelines for managing adults with 22q11.2 deletion syndrome.
Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, Danielle M Andrade, Erik Boot, Eva W C Chow, Brian Chung, Cheryl Cytrynbaum, Hanna Faghfoury, Leona Fishman,[...]. Genet Med 2015
117
30


The annual incidence of DiGeorge/velocardiofacial syndrome.
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
257
23


22q11.2 deletion syndrome: behaviour problems of children and adolescents and parental stress.
W Briegel, M Schneider, K Otfried Schwab. Child Care Health Dev 2008
26
23

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.
Jacob A S Vorstman, Monique E J Morcus, Sasja N Duijff, Petra W J Klaassen, Josien A Heineman-de Boer, Frits A Beemer, Hanna Swaab, René S Kahn, Herman van Engeland. J Am Acad Child Adolesc Psychiatry 2006
230
23

Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome.
Tamar Green, Doron Gothelf, Bronwyn Glaser, Martin Debbane, Amos Frisch, Moshe Kotler, Abraham Weizman, Stephan Eliez. J Am Acad Child Adolesc Psychiatry 2009
195
23

Developmental trajectories in 22q11.2 deletion.
Ann Swillen, Donna McDonald-McGinn. Am J Med Genet C Semin Med Genet 2015
83
23

Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome.
Kerri L Tang, Kevin M Antshel, Wanda P Fremont, Wendy R Kates. J Dev Behav Pediatr 2015
27
23

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
65
23

Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.
Lena Niklasson, Peder Rasmussen, Sólveig Oskarsdóttir, Christopher Gillberg. Res Dev Disabil 2009
139
23

Psychiatric disorders in 22q11.2 deletion syndrome are prevalent but undertreated.
S X Tang, J J Yi, M E Calkins, D A Whinna, C G Kohler, M C Souders, D M McDonald-McGinn, E H Zackai, B S Emanuel, R C Gur,[...]. Psychol Med 2014
74
15

An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome.
Kathleen Angkustsiri, Ingrid Leckliter, Nicole Tartaglia, Elliott A Beaton, Janice Enriquez, Tony J Simon. J Dev Behav Pediatr 2012
39
15

Oral health and 22q11 deletion syndrome: thoughts and experiences from the parents' perspectives.
Gunilla Klingberg, Ulrika Hallberg, Sólveig Oskarsdóttir. Int J Paediatr Dent 2010
6
33

Deficits in mental state attributions in individuals with 22q11.2 deletion syndrome (velo-cardio-facial syndrome).
Jennifer S Ho, Petya D Radoeva, Maria Jalbrzikowski, Carolyn Chow, Jessica Hopkins, Wen-Ching Tran, Ami Mehta, Nicole Enrique, Chelsea Gilbert, Kevin M Antshel,[...]. Autism Res 2012
31
15

22q11 deletion syndrome - the meaning of a diagnosis. A qualitative study on parental perspectives.
U Hallberg, S Oskarsdóttir, G Klingberg. Child Care Health Dev 2010
19
15



Patient and family experiences and opinions on adding 22q11 deletion syndrome to the newborn screen.
Abigail M Bales, Christina A Zaleski, Elizabeth W McPherson. J Genet Couns 2010
13
15

Newborn screening programs: should 22q11 deletion syndrome be added?
Abigail M Bales, Christina A Zaleski, Elizabeth W McPherson. Genet Med 2010
25
15

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
411
15

High prevalence of fatigue in adults with a 22q11.2 deletion syndrome.
Elfi Vergaelen, Stephan Claes, Stefan Kempke, Ann Swillen. Am J Med Genet A 2017
8
25

Working Memory Impairments in Chromosome 22q11.2 Deletion Syndrome: The Roles of Anxiety and Stress Physiology.
Ashley F P Sanders, Diana A Hobbs, David D Stephenson, Robert D Laird, Elliott A Beaton. J Autism Dev Disord 2017
10
20

Performance on a computerized neurocognitive battery in 22q11.2 deletion syndrome: A comparison between US and Israeli cohorts.
James J Yi, Ronnie Weinberger, Tyler M Moore, Monica E Calkins, Yael Guri, Donna M McDonald-McGinn, Elaine H Zackai, Beverly S Emanuel, Raquel E Gur, Doron Gothelf,[...]. Brain Cogn 2016
11
18

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.
R E Gur, J J Yi, D M McDonald-McGinn, S X Tang, M E Calkins, D Whinna, M C Souders, A Savitt, E H Zackai, P J Moberg,[...]. Mol Psychiatry 2014
62
15


Potential Role of Cortisol in Social and Memory Impairments in Individuals with 22q11.2 Deletion Syndrome.
Daniel Jacobson, Megan Bursch, Renee Lajiness-O'Neill. J Pediatr Genet 2016
7
28

Clinical features of 78 adults with 22q11 Deletion Syndrome.
Anne S Bassett, Eva W C Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D Webb, Michael A Gatzoulis. Am J Med Genet A 2005
288
15

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
18
15

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.
Anne S Bassett, Christian R Marshall, Anath C Lionel, Eva W C Chow, Stephen W Scherer. Hum Mol Genet 2008
128
15

The schizophrenia phenotype in 22q11 deletion syndrome.
Anne S Bassett, Eva W C Chow, Philip AbdelMalik, Mirona Gheorghiu, Janice Husted, Rosanna Weksberg. Am J Psychiatry 2003
220
15

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study.
Line Olsen, Thomas Sparsø, Shantel M Weinsheimer, Marcelo Bertalan Quintanilha Dos Santos, Wiktor Mazin, Anders Rosengren, Xabier Calle Sanchez, Louise K Hoeffding, Henriette Schmock, Marie Baekvad-Hansen,[...]. Lancet Psychiatry 2018
44
15

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
343
15

Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome.
Ania M Fiksinski, Maude Schneider, Clodagh M Murphy, Marco Armando, Stefano Vicari, Jaume M Canyelles, Doron Gothelf, Stephan Eliez, Elemi J Breetvelt, Celso Arango,[...]. Am J Med Genet A 2018
28
15

Evaluating a unique, specialist psychiatric genetic counseling clinic: uptake and impact.
A Inglis, D Koehn, B McGillivray, S E Stewart, J Austin. Clin Genet 2015
66
15

The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS).
Marianne B M van den Bree, Gregory Miller, Elizabeth Mansell, Anita Thapar, Frances Flinter, Michael J Owen. Eur J Med Genet 2013
11
18

Communication of Psychiatric Risk in 22q11.2 Deletion Syndrome: A Pilot Project.
Sarah J Hart, Kelly Schoch, Vandana Shashi, Nancy Callanan. J Genet Couns 2016
4
50


Disclosure of psychiatric manifestations of 22q11.2 deletion syndrome in medical genetics: A 12-year retrospective chart review.
Serena Talcott Baughman, Emily Morris, Kimberly Jensen, Jehannine Austin. Am J Med Genet A 2015
3
66

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.
Ian M Campbell, Sarah E Sheppard, T Blaine Crowley, Daniel E McGinn, Alice Bailey, Michael J McGinn, Marta Unolt, Jelle F Homans, Erin Y Chen, Harold I Salmons,[...]. Am J Med Genet A 2018
30
15

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.
Stephen Monks, Maria Niarchou, Aimée R Davies, James T R Walters, Nigel Williams, Michael J Owen, Marianne B M van den Bree, Kieran C Murphy. Schizophr Res 2014
50
15

Velo-cardio-facial syndrome: a review of 120 patients.
R Goldberg, B Motzkin, R Marion, P J Scambler, R J Shprintzen. Am J Med Genet 1993
343
7


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.