A citation-based method for searching scientific literature

Simone S Vaz, Bernard Chodirker, Chitra Prasad, Jamie A Seabrook, Albert E Chudley, Asuri N Prasad. Am J Med Genet A 2012
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


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
50

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
157
50


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
40

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
40

Epidemiology of holoprosencephaly: Prevalence and risk factors.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
62
40

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
30

Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research.
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,[...]. Am J Med Genet C Semin Med Genet 2011
14
30


Non-genetic risk factors for holoprosencephaly.
Candice Y Johnson, Sonja A Rasmussen. Am J Med Genet C Semin Med Genet 2010
46
30

Holoprosencephaly and ectrodactyly: Report of three new patients and review of the literature.
Amelia A Keaton, Benjamin D Solomon, Anthonie J van Essen, Kathleen M Pfleghaar, Michael A Slama, Judith A Martin, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
14
20

Morphogen to mitogen: the multiple roles of hedgehog signalling in vertebrate neural development.
Marc Fuccillo, Alexandra L Joyner, Gord Fishell. Nat Rev Neurosci 2006
299
20

Hedgehog signaling update.
M Michael Cohen. Am J Med Genet A 2010
77
20

Diabetes mellitus and birth defects.
Adolfo Correa, Suzanne M Gilboa, Lilah M Besser, Lorenzo D Botto, Cynthia A Moore, Charlotte A Hobbs, Mario A Cleves, Tiffany J Riehle-Colarusso, D Kim Waller, E Albert Reece. Am J Obstet Gynecol 2008
409
20

Epidemiology of holoprosencephaly and phenotypic characteristics of affected children: New York State, 1984-1989.
C L Olsen, J P Hughes, L G Youngblood, M Sharpe-Stimac. Am J Med Genet 1997
98
20

Genetic counseling and "molecular" prenatal diagnosis of holoprosencephaly (HPE).
Sandra Mercier, Christèle Dubourg, Marion Belleguic, Laurent Pasquier, Philippe Loget, Josette Lucas, Claude Bendavid, Sylvie Odent. Am J Med Genet C Semin Med Genet 2010
30
20

A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly.
Elaine E Stashinko, Nancy J Clegg, Heather A Kammann, Vicki T Sweet, Mauricio R Delgado, Jin S Hahn, Eric B Levey. Am J Med Genet A 2004
37
20

Management of children with holoprosencephaly.
Eric B Levey, Elaine Stashinko, Nancy J Clegg, Mauricio R Delgado. Am J Med Genet C Semin Med Genet 2010
49
20


Holoprosencephaly in the west of Scotland 1975-1994.
M L Whiteford, J L Tolmie. J Med Genet 1996
39
20

Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
110
20

Holoprosencephaly: new concepts.
E M Simon, A J Barkovich. Magn Reson Imaging Clin N Am 2001
24
20

Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtype.
A J Lewis, E M Simon, A J Barkovich, N J Clegg, M R Delgado, E Levey, J S Hahn. Neurology 2002
64
20

Neuropathology of holoprosencephaly.
Pascale Marcorelles, Annie Laquerriere. Am J Med Genet C Semin Med Genet 2010
34
20

Prenatal MR findings of the middle interhemispheric variant of holoprosencephaly.
Steven B Pulitzer, Erin M Simon, Timothy M Crombleholme, Jeffrey A Golden. AJNR Am J Neuroradiol 2004
25
20

The middle interhemispheric variant of holoprosencephaly.
Erin M Simon, Robert F Hevner, Joseph D Pinter, Nancy J Clegg, Mauricio Delgado, Stephen L Kinsman, Jin S Hahn, A James Barkovich. AJNR Am J Neuroradiol 2002
96
20

Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
43
20

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
20

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
20

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
20

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
20

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
20

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
20


Syndromes associated with holoprosencephaly.
Paul Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
25
20

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
20

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
20

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
20

Holoprosencephaly in the genomics era.
Erich Roessler, Ping Hu, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
24
20

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
20

Molecular testing in holoprosencephaly.
Paul Kruszka, Ariel F Martinez, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
11
20

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
20

Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly.
Artem Kim, Clara Savary, Christèle Dubourg, Wilfrid Carré, Charlotte Mouden, Houda Hamdi-Rozé, Hélène Guyodo, Jerome Le Douce, Laurent Pasquier, Elisabeth Flori,[...]. Brain 2019
21
20

New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
Sandra Mercier, Christèle Dubourg, Nicolas Garcelon, Boris Campillo-Gimenez, Isabelle Gicquel, Marion Belleguic, Leslie Ratié, Laurent Pasquier, Philippe Loget, Claude Bendavid,[...]. J Med Genet 2011
76
20


The role of regional posterior frontal dura mater in the overlying suture morphology.
Bethany J Slater, Matthew D Kwan, Deepak M Gupta, Jacqueline K Lee, Michael T Longaker. Plast Reconstr Surg 2009
19
10



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.