A citation-based method for searching scientific literature

Céline Poirsier, Justine Besseau-Ayasse, Caroline Schluth-Bolard, Jérôme Toutain, Chantal Missirian, Cédric Le Caignec, Anne Bazin, Marie Christine de Blois, Paul Kuentz, Marie Catty, Agnès Choiset, Ghislaine Plessis, Audrey Basinko, Pascaline Letard, Elisabeth Flori, Mélanie Jimenez, Mylène Valduga, Emilie Landais, Hakima Lallaoui, François Cartault, James Lespinasse, Dominique Martin-Coignard, Patrick Callier, Céline Pebrel-Richard, Marie-France Portnoi, Tiffany Busa, Aline Receveur, Florence Amblard, Catherine Yardin, Radu Harbuz, Fabienne Prieur, Nathalie Le Meur, Eva Pipiras, Pascale Kleinfinger, François Vialard, Martine Doco-Fenzy. Eur J Hum Genet 2016
Times Cited: 23







List of co-cited articles
164 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
411
52

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Laetitia Gouas, Nina Horelli-Kuitunen, Kwong Wai Choy, Sandra García-Herrero, Alberto Gonzalez de la Vega,[...]. Prenat Diagn 2015
161
34

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
821
30

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
30

Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.
S J Gross, M Stosic, D M McDonald-McGinn, A S Bassett, A Norvez, R Dhamankar, K Kobara, E Kirkizlar, B Zimmermann, N Wayham,[...]. Ultrasound Obstet Gynecol 2016
65
30


Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
26

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
26

Clinical features and follow-up in patients with 22q11.2 deletion syndrome.
Caterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, Annarosa Soresina, Silvana Martino, Roberto Rondelli, Rita Consolini, Ezia Maria Ruga, Fabio Cardinale, Andrea Finocchi,[...]. J Pediatr 2014
80
21

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
21

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
21

Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome.
Mi-Young Lee, Hye-Sung Won, Ju Won Baek, Jae-Hyun Cho, Jae-Yoon Shim, Pil-Ryang Lee, Ahm Kim. Obstet Gynecol Sci 2014
12
33

Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching.
D B McElhinney, B J Clark, P M Weinberg, M L Kenton, D McDonald-McGinn, D A Driscoll, E H Zackai, E Goldmuntz. J Am Coll Cardiol 2001
154
17

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
17

Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing.
J Helgeson, J Wardrop, T Boomer, E Almasri, W B Paxton, J S Saldivar, N Dharajiya, T J Monroe, D H Farkas, D S Grosu,[...]. Prenat Diagn 2015
79
17

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!
D M McDonald-McGinn, M K Tonnesen, A Laufer-Cahana, B Finucane, D A Driscoll, B S Emanuel, E H Zackai. Genet Med 2001
202
17

A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes.
J Besseau-Ayasse, C Violle-Poirsier, A Bazin, N Gruchy, A Moncla, F Girard, M Till, F Mugneret, A Coussement, F Pelluard,[...]. Prenat Diagn 2014
35
17

22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases.
Shabnam Peyvandi, Philip J Lupo, Jennifer Garbarini, Stacy Woyciechowski, Sharon Edman, Beverly S Emanuel, Laura E Mitchell, Elizabeth Goldmuntz. Pediatr Cardiol 2013
56
17

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
180
17


Detailed analysis of 22q11.2 with a high density MLPA probe set.
G R Jalali, J A S Vorstman, Ab Errami, R Vijzelaar, J Biegel, T Shaikh, B S Emanuel. Hum Mutat 2008
71
17

Presenting phenotype in 100 children with the 22q11 deletion syndrome.
Sólveig Oskarsdóttir, Christina Persson, Bengt O Eriksson, Anders Fasth. Eur J Pediatr 2005
115
17

Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
Lidia Ziolkowska, Wanda Kawalec, Anna Turska-Kmiec, Malgorzata Krajewska-Walasek, Grazyna Brzezinska-Rajszys, Jadwiga Daszkowska, Bogdan Maruszewski, Piotr Burczynski. Eur J Pediatr 2008
47
17

Frequency of 22q11 deletions in patients with conotruncal defects.
E Goldmuntz, B J Clark, L E Mitchell, A F Jawad, B F Cuneo, L Reed, D McDonald-McGinn, P Chien, J Feuer, E H Zackai,[...]. J Am Coll Cardiol 1998
359
17

Prenatal diagnosis and outcome of right aortic arch without significant intracardiac anomaly.
Yaron Razon, Michael Berant, Rami Fogelman, Gabriel Amir, Einat Birk. J Am Soc Echocardiogr 2014
44
13

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
235
13

Microduplication 22q11.2: a new chromosomal syndrome.
Marie-France Portnoï. Eur J Med Genet 2009
149
13


Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization.
M Chen, Y-S Yang, J-C Shih, W-H Lin, D-J Lee, Y-S Lin, C-H Chou, A D Cameron, N A Ginsberg, C-A Chen,[...]. Ultrasound Obstet Gynecol 2014
17
17

Central 22q11.2 deletions.
Patrick Rump, Nicole de Leeuw, Anthonie J van Essen, Corien C Verschuuren-Bemelmans, Hermine E Veenstra-Knol, Mariëlle E M Swinkels, Wilma Oostdijk, Claudia Ruivenkamp, Willie Reardon, Sonja de Munnik,[...]. Am J Med Genet A 2014
38
13

Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
526
13

Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
Anna Wozniak, Danuta Wolnik-Brzozowska, Marzena Wisniewska, Renata Glazar, Anna Materna-Kiryluk, Tomasz Moszura, Magdalena Badura-Stronka, Joanna Skolozdrzy, Maciej R Krawczynski, Joanna Zeyland,[...]. BMC Pediatr 2010
16
18

Mouse and human CRKL is dosage sensitive for cardiac outflow tract formation.
Silvia E Racedo, Donna M McDonald-McGinn, Jonathan H Chung, Elizabeth Goldmuntz, Elaine Zackai, Beverly S Emanuel, Bin Zhou, Birgit Funke, Bernice E Morrow. Am J Hum Genet 2015
38
13

Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.
Florence Bretelle, Laura Beyer, Marie Christine Pellissier, Chantal Missirian, Sabine Sigaudy, Marc Gamerre, Claude D'Ercole, Nicole Philip. Eur J Med Genet 2010
31
13

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
13

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS.
Donna M McDonald-McGinn, Somayyeh Fahiminiya, Timothée Revil, Beata A Nowakowska, Joshua Suhl, Alice Bailey, Elisabeth Mlynarski, David R Lynch, Albert C Yan, Larissa T Bilaniuk,[...]. J Med Genet 2013
74
13

Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome.
Chrystal Chan, Gregory Costain, Lucas Ogura, Candice K Silversides, Eva W C Chow, Anne S Bassett. J Genet Couns 2015
13
23

Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome.
Evelyn Ning Man Cheung, Susan R George, Danielle M Andrade, Eva W C Chow, Candice K Silversides, Anne S Bassett. Genet Med 2014
46
13


Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
Jacob A S Vorstman, Elemi J Breetvelt, Sasja N Duijff, Stephan Eliez, Maude Schneider, Maria Jalbrzikowski, Marco Armando, Stefano Vicari, Vandana Shashi, Stephen R Hooper,[...]. JAMA Psychiatry 2015
120
13


Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome.
Tingwei Guo, Jonathan H Chung, Tao Wang, Donna M McDonald-McGinn, Wendy R Kates, Wanda Hawuła, Karlene Coleman, Elaine Zackai, Beverly S Emanuel, Bernice E Morrow. Am J Hum Genet 2015
36
13

Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.
Fabíola P Monteiro, Társis P Vieira, Ilária C Sgardioli, Miriam C Molck, Ana Paula Damiano, Josiane Souza, Isabella L Monlleó, Marshall I B Fontes, Agnes C Fett-Conte, Têmis M Félix,[...]. Eur J Pediatr 2013
35
13

22q11 deletion syndrome: current perspective.
Bülent Hacıhamdioğlu, Duygu Hacıhamdioğlu, Kenan Delil. Appl Clin Genet 2015
40
13

Phenotypic variability of atypical 22q11.2 deletions not including TBX1.
Judith M A Verhagen, Karin E M Diderich, Grétel Oudesluijs, Grazia M S Mancini, Alex J Eggink, Anna C Verkleij-Hagoort, Irene A L Groenenberg, Patrick J Willems, Frederik A du Plessis, Stella A de Man,[...]. Am J Med Genet A 2012
40
13

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
D A Driscoll, J Salvin, B Sellinger, M L Budarf, D M McDonald-McGinn, E H Zackai, B S Emanuel. J Med Genet 1993
404
13

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.
R J Shprintzen, R B Goldberg, M L Lewin, E J Sidoti, M D Berkman, R V Argamaso, D Young. Cleft Palate J 1978
513
13

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
687
13




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.