A citation-based method for searching scientific literature

Natario L Couser, Chetna K Pande, Jonathan M Walsh, James Tepperberg, Arthur S Aylsworth. Am J Med Genet A 2017
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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
100

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
66

Skeletal anomalies and deformities in patients with deletions of 22q11.
J E Ming, D M McDonald-McGinn, T E Megerian, D A Driscoll, E R Elias, B M Russell, M Irons, B S Emanuel, R I Markowitz, E H Zackai. Am J Med Genet 1997
63
66

Fetal phenotype associated with the 22q11 deletion.
Anne-Claire Noël, Fanny Pelluard, Anne-Lise Delezoide, Louise Devisme, Laurence Loeuillet, Brigitte Leroy, Alain Martin, Raymonde Bouvier, Annie Laquerriere, Corinne Jeanne-Pasquier,[...]. Am J Med Genet A 2014
27
66

Presenting phenotype in 100 children with the 22q11 deletion syndrome.
Sólveig Oskarsdóttir, Christina Persson, Bengt O Eriksson, Anders Fasth. Eur J Pediatr 2005
115
66

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
33

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
105
33

Multidigit camptodactyly of the hands and feet: A case study.
Kristy L Hamilton, David T Netscher. Hand (N Y) 2013
7
33

Association of anterior glottic webs with velocardiofacial syndrome (chromosome 22q11.2 deletion).
R Christopher Miyamoto, Robin T Cotton, Alan F Rope, Robert J Hopkin, Aliza P Cohen, Sally R Shott, Michael J Rutter. Otolaryngol Head Neck Surg 2004
45
33

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
33


Laryngeal abnormalities are frequent in the 22q11 deletion syndrome.
C Leopold, A De Barros, C Cellier, V Drouin-Garraud, D Dehesdin, J-P Marie. Int J Pediatr Otorhinolaryngol 2012
22
33

The neurocognitive phenotype in velo-cardio-facial syndrome: a developmental perspective.
Kevin M Antshel, Wanda Fremont, Wendy R Kates. Dev Disabil Res Rev 2008
56
33

Proposal of a new classification for optimising outcome assessment following partial cricotracheal resections in severe pediatric subglottic stenosis.
Philippe Monnier, Christos Ikonomidis, Yves Jaquet, Mercy George. Int J Pediatr Otorhinolaryngol 2009
21
33

Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
Kathleen E Sullivan. Immunol Allergy Clin North Am 2008
61
33

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.
Elisabeth E Mlynarski, Michael Xie, Deanne Taylor, Molly B Sheridan, Tingwei Guo, Silvia E Racedo, Donna M McDonald-McGinn, Eva W C Chow, Jacob Vorstman, Ann Swillen,[...]. Hum Genet 2016
27
33

Elements of morphology: standard terminology for the hands and feet.
Leslie G Biesecker, Jon M Aase, Carol Clericuzio, Fiorella Gurrieri, I Karen Temple, Helga Toriello. Am J Med Genet A 2009
57
33

22q11 deletion syndrome: current perspective.
Bülent Hacıhamdioğlu, Duygu Hacıhamdioğlu, Kenan Delil. Appl Clin Genet 2015
40
33

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
33

Velocardiofacial syndrome presenting as distal arthrogryposis.
Koen Devriendt, Ann Swillen, Marc Gewillig, Jean-Pierre Fryns, Pierre Moens, Luc De Smet. Eur J Pediatr 2004
4
33

Camptodactyly: classification and results of nonoperative treatment.
L S Benson, P M Waters, N I Kamil, B P Simmons, J Upton. J Pediatr Orthop 1994
27
33

LARYNGEAL WEB ASSOCIATED WITH CHROMOSOME 22q11 DELETION IN A PRETERM INFANT.
B Vatansever, G Demirel, S Gundogdu, S Yilmaz-Semerci, M Gunduz, S Oktem, A Tastekin. Genet Couns 2015
1
100

Anomalies of the intrinsic muscles in camptodactyly.
R M McFarlane, G I Curry, H B Evans. J Hand Surg Am 1983
30
33


Proposed grading system for subglottic stenosis based on endotracheal tube sizes.
C M Myer, D M O'Connor, R T Cotton. Ann Otol Rhinol Laryngol 1994
466
33

Camptodactyly Treatment for the Lesser Digits.
Lindley B Wall, Marybeth Ezaki, Charles A Goldfarb. J Hand Surg Am 2018
2
50

DiGeorge syndrome: still an enigma.
R Parkman, K Weinberg. J Pediatr 1998
3
33

Dupuytren's disease in children-differential diagnosis.
M Rhomberg, C Rainer, A Gardetto, H Piza-Katzer. J Pediatr Surg 2002
11
33

Dupuytren in a Child: Rare Presentation of a Rare Clinical Entity.
Georgia-Alexandra Spyropoulou, Leonidas Pavlidis, Panagiotis Milothridis, Thomas Zaraboukas, Efterpi Demiri. J Hand Surg Am 2016
4
33

MOC-PS(SM) CME article: Dupuytren's disease.
William M Swartz, Donald H Lalonde. Plast Reconstr Surg 2008
18
33

Metabolic syndrome in psychiatric patients: overview, mechanisms, and implications.
Brenda W J H Penninx, Sjors M M Lange. Dialogues Clin Neurosci 2018
56
33

The CHD8 overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patients.
Philip J Ostrowski, Anna Zachariou, Chey Loveday, Ana Beleza-Meireles, Marta Bertoli, John Dean, Andrew G L Douglas, Ian Ellis, Alison Foster, John M Graham,[...]. Am J Med Genet C Semin Med Genet 2019
15
33

U.S. householder survey of functional gastrointestinal disorders. Prevalence, sociodemography, and health impact.
D A Drossman, Z Li, E Andruzzi, R D Temple, N J Talley, W G Thompson, W E Whitehead, J Janssens, P Funch-Jensen, E Corazziari. Dig Dis Sci 1993
33


Neurofibromatosis type 1.
David H Gutmann, Rosalie E Ferner, Robert H Listernick, Bruce R Korf, Pamela L Wolters, Kimberly J Johnson. Nat Rev Dis Primers 2017
218
33


Williams syndrome.
Mark D Twite, Scott Stenquist, Richard J Ing. Paediatr Anaesth 2019
11
33

A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
Poh Hui Chia, Franklin Lei Zhong, Shinsuke Niwa, Carine Bonnard, Kagistia Hana Utami, Ruizhu Zeng, Hane Lee, Ascia Eskin, Stanley F Nelson, William H Xie,[...]. Elife 2018
21
33

Disorders of sex development.
Selma Feldman Witchel. Best Pract Res Clin Obstet Gynaecol 2018
30
33

Behavior and sleep disturbance in Smith-Magenis syndrome.
Brian J Shayota, Sarah H Elsea. Curr Opin Psychiatry 2019
8
33

Health status of children with moderate to severe cerebral palsy.
G S Liptak, M O'Donnell, M Conaway, W C Chumlea, G Wolrey, R C Henderson, E Fung, V A Stallings, L Samson-Fang, R Calvert,[...]. Dev Med Child Neurol 2001
148
33

47,XXX: what is the prognosis?
M G Linden, B G Bender, R J Harmon, D A Mrazek, A Robinson. Pediatrics 1988
67
33

A case of Costello with parathyroid adenoma and hyperprolactinemia.
Mehtap Cakir, Cumhur Arici, Sukran Tacoy, Umit Karayalcin. Am J Med Genet A 2004
11
33

Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYY.
Nicole R Tartaglia, Rebecca Wilson, Judith S Miller, Jessica Rafalko, Lisa Cordeiro, Shanlee Davis, David Hessl, Judith Ross. J Dev Behav Pediatr 2017
46
33

CHARGE syndrome gastrointestinal involvement: from mouth to anus.
A Hudson, M Macdonald, J N Friedman, K Blake. Clin Genet 2017
9
33

Cardiovascular risk factors improve during 3 years of growth hormone therapy in Prader-Willi syndrome.
D l'Allemand, U Eiholzer, M Schlumpf, H Steinert, W Riesen. Eur J Pediatr 2000
30
33

A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndrome.
R Day, B Beckett, D Donnai, A Fryer, M Heidenblad, P Howard, B Kerr, S Mansour, U Maye, S McKee,[...]. Clin Genet 2008
20
33

Adrenal insufficiency in Smith-Lemli-Opitz syndrome.
H C Andersson, J Frentz, J E Martínez, C M Tuck-Muller, J Bellizaire. Am J Med Genet 1999
35
33

Deletion in chromosome region 22q11 in a child with CHARGE association.
K Devriendt, A Swillen, J P Fryns. Clin Genet 1998
32
33

Systematic assessment of atypical deletions reveals genotype-phenotype correlation in 22q11.2.
A Rauch, S Zink, C Zweier, C T Thiel, A Koch, R Rauch, J Lascorz, U Hüffmeier, M Weyand, H Singer,[...]. J Med Genet 2005
109
33


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.