A citation-based method for searching scientific literature

Nir Friedman, Shlomit Rienstein, Yonatan Yeshayahu, Doron Gothelf, Raz Somech. Clin Pediatr (Phila) 2016
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


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
80


Prevalence of 22q11 microdeletion.
S Tézenas Du Montcel, H Mendizabai, S Aymé, A Lévy, N Philip. J Med Genet 1996
194
60

A population study of chromosome 22q11 deletions in infancy.
J Goodship, I Cross, J LiLing, C Wren. Arch Dis Child 1998
180
60

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
60

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
40

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
40

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
40

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
40

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
40

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
40

Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome.
Evelyn Ning Man Cheung, Susan R George, Gary A Costain, Danielle M Andrade, Eva W C Chow, Candice K Silversides, Anne S Bassett. Clin Endocrinol (Oxf) 2014
40
40

DiGeorge Syndrome: a not so rare disease.
Angela B F Fomin, Antonio Carlos Pastorino, Chong Ae Kim, C A Pereira, Magda Carneiro-Sampaio, Cristina Miuki Abe-Jacob. Clinics (Sao Paulo) 2010
24
40


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
40

Detection of microdeletion 22q11.2 in a fetus by next-generation sequencing of maternal plasma.
Taylor J Jensen, Zeljko Dzakula, Cosmin Deciu, Dirk van den Boom, Mathias Ehrich. Clin Chem 2012
84
20

Personal utility and genomic information: look before you leap.
Scott D Grosse, Colleen M McBride, James P Evans, Muin J Khoury. Genet Med 2009
57
20

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
20

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
20

Maternal cell-free DNA-based screening for fetal microdeletion and the importance of careful diagnostic follow-up.
Svetlana A Yatsenko, David G Peters, Devereux N Saller, Tianjiao Chu, Michelle Clemens, Aleksandar Rajkovic. Genet Med 2015
28
20

Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.
T K Lau, S W Cheung, P S S Lo, A N Pursley, M K Chan, F Jiang, H Zhang, W Wang, L F J Jong, O K C Yuen,[...]. Ultrasound Obstet Gynecol 2014
95
20

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
20

What is the clinical utility of genetic testing?
Scott D Grosse, Muin J Khoury. Genet Med 2006
176
20

Noninvasive prenatal diagnosis of a fetal microdeletion syndrome.
David Peters, Tianjiao Chu, Svetlana A Yatsenko, Nancy Hendrix, W Allen Hogge, Urvashi Surti, Kimberly Bunce, Mary Dunkel, Patricia Shaw, Aleksandar Rajkovic. N Engl J Med 2011
92
20

Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.
H Zhang, Y Gao, F Jiang, M Fu, Y Yuan, Y Guo, Z Zhu, M Lin, Q Liu, Z Tian,[...]. Ultrasound Obstet Gynecol 2015
193
20

Clinical implementation of cell-free DNA-based aneuploidy screening: perspectives from a national audit.
L Hui, M Teoh, F da Silva Costa, P Ramsay, R Palma-Dias, Z Richmond, S Piessens, S Walker. Ultrasound Obstet Gynecol 2015
34
20

Screening newborn blood spots for 22q11.2 deletion syndrome using multiplex droplet digital PCR.
Dalyir Pretto, Dianna Maar, Carolyn M Yrigollen, Jack Regan, Flora Tassone. Clin Chem 2015
21
20

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
20

Current Status of Testing for Microdeletion Syndromes and Rare Autosomal Trisomies Using Cell-Free DNA Technology.
Yuval Yaron, Jacques Jani, Maximilian Schmid, Dick Oepkes. Obstet Gynecol 2015
32
20

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
274
20

DNA sequencing versus standard prenatal aneuploidy screening.
Diana W Bianchi, R Lamar Parker, Jeffrey Wentworth, Rajeevi Madankumar, Craig Saffer, Anita F Das, Joseph A Craig, Darya I Chudova, Patricia L Devers, Keith W Jones,[...]. N Engl J Med 2014
392
20

Impact of noninvasive prenatal testing in regionally dispersed medical centers in the United States.
Lawrence D Platt, Mary Beth Janicki, Tracy Prosen, James D Goldberg, Joseph Adashek, Reinaldo Figueroa, John Rodis, Wayne Liao, Amy J Sehnert, Holly L Snyder,[...]. Am J Obstet Gynecol 2014
35
20

Newborn screening programs: should 22q11 deletion syndrome be added?
Abigail M Bales, Christina A Zaleski, Elizabeth W McPherson. Genet Med 2010
25
20

Cell-free DNA analysis for noninvasive examination of trisomy.
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
392
20

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
20



Vitamin D deficiency in Korean children: prevalence, risk factors, and the relationship with parathyroid hormone levels.
In Hyuk Chung, Hae Jung Kim, Sochung Chung, Eun-Gyong Yoo. Ann Pediatr Endocrinol Metab 2014
16
20

Symptomatic anal anomalies in chromosome 22q11 deletion syndrome: a report of three patients.
Mudaffer Al-Mudaffer, Prem Puri, William Reardon. Pediatr Surg Int 2006
4
25

The spectrum of parathyroid gland dysfunction associated with the microdeletion 22q11.
Sylvie Hiéronimus, Magali Bec-Roche, Florence Pedeutour, Jean Claude Lambert, Kathy Wagner-Malher, Jean Christophe Mas, Jean Louis Sadoul, Patrick Fénichel. Eur J Endocrinol 2006
27
20

1
100

Hypoparathyroidism and 22q11 deletion syndrome.
S C Taylor, G Morris, D Wilson, S J Davies, J W Gregory. Arch Dis Child 2003
34
20

Premature death in adults with 22q11.2 deletion syndrome.
A S Bassett, E W C Chow, J Husted, K A Hodgkinson, E Oechslin, L Harris, C Silversides. J Med Genet 2009
59
20

Delayed-onset hypoparathyroidism in an adolescent with chromosome 22Q11 deletion syndrome.
Jaspreet S Kambo, Christian M Girgis, Bernard L Champion, Jack R Wall. Endocr Pract 2011
3
33


Anorectal malformation: the etiological factors.
Chen Wang, Long Li, Wei Cheng. Pediatr Surg Int 2015
27
20

Two cases of chromosome 22q11.2 deletion syndrome diagnosed in 12-year-old boys with hypocalcemic seizures.
Jae Won Hyun, Hwa Kyoung Chung, Sung-Hee Kim, Ye Ji Choi, Sung Jin Kim, Hae Soon Kim, Hyang Woon Lee. J Epilepsy Res 2012
1
100

A patient with 22q11.2 deletion syndrome: case report.
Sema Kabataş Eryılmaz, Firdevs Baş, Ali Satan, Feyza Darendeliler, Rüveyde Bundak, Hülya Günöz, Nurçin Saka. J Clin Res Pediatr Endocrinol 2009
3
33

DiGeorge syndrome presenting as late onset hypocalcaemia in adulthood.
Philip C Johnston, Deirdre E Donnelly, Patrick J Morrison, Steven J Hunter. Ulster Med J 2008
7
20

An adult case of 22q11.2 deletion syndrome diagnosed in a 36-year-old woman with hypocalcemia caused by hypoparathyroidism and Hashimoto's thyroiditis.
Yuki Nakada, Ken Terui, Kazunori Kageyama, Yuko Tsushima, Hiroshi Murakami, Yasushi Soma, Takeshi Nigawara, Satoru Sakihara. Intern Med 2013
8
20


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.