A citation-based method for searching scientific literature

Iêda M Orioli, Emmanuelle Amar, Marian K Bakker, Eva Bermejo-Sánchez, Fabrizio Bianchi, Mark A Canfield, Maurizio Clementi, Adolfo Correa, Melinda Csáky-Szunyogh, Marcia L Feldkamp, Danielle Landau, Emanuele Leoncini, Zhu Li, R Brian Lowry, Pierpaolo Mastroiacovo, Margery Morgan, Osvaldo M Mutchinick, Anke Rissmann, Annukka Ritvanen, Gioacchino Scarano, Elena Szabova, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2011
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
157
28

Risk factors for non-syndromic holoprosencephaly in the National Birth Defects Prevention Study.
Eric A Miller, Sonja A Rasmussen, Anna Maria Siega-Riz, Jaime L Frías, Margaret A Honein. Am J Med Genet C Semin Med Genet 2010
43
28

Analysis of genotype-phenotype correlations in human holoprosencephaly.
Benjamin D Solomon, Sandra Mercier, Jorge I Vélez, Daniel E Pineda-Alvarez, Adrian Wyllie, Nan Zhou, Christèle Dubourg, Veronique David, Sylvie Odent, Erich Roessler,[...]. Am J Med Genet C Semin Med Genet 2010
107
21

Holoprosencephaly in infants of diabetic mothers.
M Barr, J W Hanson, K Currey, S Sharp, H Toriello, R D Schmickel, G N Wilson. J Pediatr 1983
159
21

Risk factors for nonsyndromic holoprosencephaly: a Manitoba case-control study.
Simone S Vaz, Bernard Chodirker, Chitra Prasad, Jamie A Seabrook, Albert E Chudley, Asuri N Prasad. Am J Med Genet A 2012
10
30


Non-genetic risk factors for holoprosencephaly.
Candice Y Johnson, Sonja A Rasmussen. Am J Med Genet C Semin Med Genet 2010
46
21

Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations.
Emanuele Leoncini, Giovanni Baranello, Iêda M Orioli, Göran Annerén, Marian Bakker, Fabrizio Bianchi, Carol Bower, Mark A Canfield, Eduardo E Castilla, Guido Cocchi,[...]. Birth Defects Res A Clin Mol Teratol 2008
64
21

Cloacal exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research.
Marcia L Feldkamp, Lorenzo D Botto, Emmanuelle Amar, Marian K Bakker, Eva Bermejo-Sánchez, Sebastiano Bianca, Mark A Canfield, Eduardo E Castilla, Maurizio Clementi, Melinda Csaky-Szunyogh,[...]. Am J Med Genet C Semin Med Genet 2011
31
14

Sirenomelia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review.
Iêda M Orioli, Emmanuelle Amar, Jazmin Arteaga-Vazquez, Marian K Bakker, Sebastiano Bianca, Lorenzo D Botto, Maurizio Clementi, Adolfo Correa, Melinda Csaky-Szunyogh, Emanuele Leoncini,[...]. Am J Med Genet C Semin Med Genet 2011
44
14

A joint international study on the epidemiology of hypospadias.
B Källén, R Bertollini, E Castilla, A Czeizel, L B Knudsen, M L Martinez-Frias, P Mastroiacovo, O Mutchinick. Acta Paediatr Scand Suppl 1986
103
14

Trends of selected malformations in relation to folic acid recommendations and fortification: an international assessment.
Lorenzo D Botto, Alessandra Lisi, Carol Bower, Mark A Canfield, Nirupa Dattani, Catherine De Vigan, Hermien De Walle, David J Erickson, Jane Halliday, Lorentz M Irgens,[...]. Birth Defects Res A Clin Mol Teratol 2006
75
14

Conjoined twins: a worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research.
Osvaldo M Mutchinick, Leonora Luna-Muñoz, Emmanuelle Amar, Marian K Bakker, Maurizio Clementi, Guido Cocchi, Maria da Graça Dutra, Marcia L Feldkamp, Danielle Landau, Emanuele Leoncini,[...]. Am J Med Genet C Semin Med Genet 2011
72
14

Bladder exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature.
Csaba Siffel, Adolfo Correa, Emmanuelle Amar, Marian K Bakker, Eva Bermejo-Sánchez, Sebastiano Bianca, Eduardo E Castilla, Maurizio Clementi, Guido Cocchi, Melinda Csáky-Szunyogh,[...]. Am J Med Genet C Semin Med Genet 2011
37
14

Valproic acid and spina bifida.
T Bjerkedal, A Czeizel, J Goujard, B Kallen, P Mastroiacova, N Nevin, G Oakley, E Robert. Lancet 1982
213
14

The cyclops and the mermaid: an epidemiological study of two types of rare malformation.
B Källén, E E Castilla, P A Lancaster, O Mutchinick, L B Knudsen, M L Martínez-Frías, P Mastroiacovo, E Robert. J Med Genet 1992
64
14


Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
14


The teratogenic effects of prenatal ethanol exposure are exacerbated by Sonic Hedgehog or GLI2 haploinsufficiency in the mouse.
Henry W Kietzman, Joshua L Everson, Kathleen K Sulik, Robert J Lipinski. PLoS One 2014
74
14

Case of true cyclopia.
H J Garzozi, S Barkay. Br J Ophthalmol 1985
12
16

Segregation analysis in nonsyndromic holoprosencephaly.
S Odent, B Le Marec, A Munnich, M Le Merrer, C Bonaïti-Pellié. Am J Med Genet 1998
43
14

Associations between maternal periconceptional exposure to secondhand tobacco smoke and major birth defects.
Adrienne T Hoyt, Mark A Canfield, Paul A Romitti, Lorenzo D Botto, Marlene T Anderka, Sergey V Krikov, Morgan K Tarpey, Marcia L Feldkamp. Am J Obstet Gynecol 2016
31
14

Maternal obesity, gestational diabetes, and central nervous system birth defects.
James L Anderson, D Kim Waller, Mark A Canfield, Gary M Shaw, Margaret L Watkins, Martha M Werler. Epidemiology 2005
148
14



Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation.
Jin S Hahn, Patrick D Barnes. Am J Med Genet C Semin Med Genet 2010
93
14

Dose-dependent teratogenicity of the synthetic cannabinoid CP-55,940 in mice.
Marcoita T Gilbert, Kathleen K Sulik, Eric W Fish, Lorinda K Baker, Deborah B Dehart, Scott E Parnell. Neurotoxicol Teratol 2016
23
14

Self-reported maternal smoking during pregnancy by source in Utah, 2003-2007.
Sivithee Srisukhumbowornchai, Sergey Krikov, Marcia L Feldkamp. Birth Defects Res A Clin Mol Teratol 2012
18
14

[From teratology to mythology: ancient legends].
A Stahl, P Tourame. Arch Pediatr 2010
8
25

True cyclopia-very rare anomaly.
K R Srinivasan, N Abraham Ratna Joseph, P Koteswary. J Clin Diagn Res 2014
3
66

Nongenetic risk factors for holoprosencephaly: An updated review of the epidemiologic literature.
April D Summers, Jennita Reefhuis, Joanna Taliano, Sonja A Rasmussen. Am J Med Genet C Semin Med Genet 2018
5
40

Definition of critical periods for Hedgehog pathway antagonist-induced holoprosencephaly, cleft lip, and cleft palate.
Galen W Heyne, Cal G Melberg, Padydeh Doroodchi, Kia F Parins, Henry W Kietzman, Joshua L Everson, Lydia J Ansen-Wilson, Robert J Lipinski. PLoS One 2015
39
14

Validation of self-reported proximity to agricultural crops in a case-control study of neural tube defects.
Rudolph P Rull, Beate Ritz, Gary M Shaw. J Expo Sci Environ Epidemiol 2006
22
14


Syndromes associated with holoprosencephaly.
Paul Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
25
14

A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly.
Paul Kruszka, Seth I Berger, Karin Weiss, Joshua L Everson, Ariel F Martinez, Sungkook Hong, Kwame Anyane-Yeboa, Robert J Lipinski, Maximilian Muenke. Am J Hum Genet 2019
14
14

Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly.
I M Orioli, E E Castilla, J E Ming, J Nazer, M J Burle de Aguiar, J C Llerena, M Muenke. Hum Genet 2001
41
14

Williams-Beuren syndrome in diverse populations.
Paul Kruszka, Antonio R Porras, Deise Helena de Souza, Angélica Moresco, Victoria Huckstadt, Ashleigh D Gill, Alec P Boyle, Tommy Hu, Yonit A Addissie, Gary T K Mok,[...]. Am J Med Genet A 2018
36
14

Holoprosencephaly in the genomics era.
Erich Roessler, Ping Hu, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
24
14

Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling.
Erich Roessler, Ping Hu, Juliana Marino, Sungkook Hong, Rachel Hart, Seth Berger, Ariel Martinez, Yu Abe, Paul Kruszka, James W Thomas,[...]. Hum Mutat 2018
16
14

Molecular testing in holoprosencephaly.
Paul Kruszka, Ariel F Martinez, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
11
18

Using satellite derived land cover information for a multi-temporal study of self-reported recall of proximity to farmland.
Gillian A Avruskin, Jaymie R Meliker, Geoffrey M Jacquez. J Expo Sci Environ Epidemiol 2008
5
40

Epidemiological characteristics of holoprosencephaly in China, 2007-2014: A retrospective study based on the national birth defects surveillance system.
Ling Yi, Zhongqiang Liu, Changfei Deng, Xiaohong Li, Ke Wang, Kui Deng, Yi Mu, Jun Zhu, Qi Li, Yanping Wang,[...]. PLoS One 2019
5
40

Gene-Environment Interactions and the Etiology of Birth Defects.
Robert S Krauss, Mingi Hong. Curr Top Dev Biol 2016
38
14

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
14

Cyclopia: a rare condition with unusual presentation - a case report.
Ghassan Sa Salama, Mahmoud Af Kaabneh, Mohamed K Al-Raqad, Ibrahim Mh Al-Abdallah, Ayoub Ga Shakkoury, Ruba Aa Halaseh. Clin Med Insights Pediatr 2015
6
33



Increasing total prevalence rate of cases with Down syndrome in Hungary.
Julia Métneki, Andrew E Czeizel. Eur J Epidemiol 2005
18
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.