A citation-based method for searching scientific literature

Jarosław Swatek, Justyna Szumiło, Franciszek Burdan. Reprod Toxicol 2013
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Embryogenesis of holoprosencephaly.
Kohei Shiota, Shigehito Yamada, Munekazu Komada, Makoto Ishibashi. Am J Med Genet A 2007
19
100

Development and tissue origins of the mammalian cranial base.
B McBratney-Owen, S Iseki, S D Bamforth, B R Olsen, G M Morriss-Kay. Dev Biol 2008
143
50

3-D reconstruction of a human fetus with combined holoprosencephaly and cyclopia.
Wolfgang H Arnold, Veronika Meiselbach. Head Face Med 2009
8
50

Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
131
50

Cyclopia: craniofacial appearance on MR and three-dimensional CT.
D P Liu, D M Burrowes, M N Qureshi. AJNR Am J Neuroradiol 1997
6
50

Teratogen-mediated inhibition of target tissue response to Shh signaling.
M K Cooper, J A Porter, K E Young, P A Beachy. Science 1998
698
50

The developing anterior skull base: CT appearance from birth to 2 years of age.
C J Belden, A A Mancuso, I M Kotzur. AJNR Am J Neuroradiol 1997
36
50

Cyclopia: a radiological and anatomical craniofacial post mortem study.
C Cannistrá, P Barbet, P Parisi, G Iannetti. J Craniomaxillofac Surg 2001
8
50

Otx2 and HNF3beta genetically interact in anterior patterning.
O Jin, K Harpal, S L Ang, J Rossant. Int J Dev Biol 2001
30
50

MR, CT, and plain film imaging of the developing skull base in fetal specimens.
W R Nemzek, H A Brodie, S T Hecht, B W Chong, C J Babcook, J A Seibert. AJNR Am J Neuroradiol 2000
60
50


Cyclopia and proboscis - the extreme end of holoprosencephaly.
Andrei Mihai Măluţan, Marina Dudea, Răzvan Ciortea, Mihaela Mureşan, Carmen Elena Bucuri, Carina Mihu, Dan Mihu. Rom J Morphol Embryol 2017
3
50



The oral manifestations of cyclopia. Review of the literature and report of two cases.
H O SEDANO, R J GORLIN. Oral Surg Oral Med Oral Pathol 1963
24
50

Investigation of a cyclopic, human, term fetus by use of magnetic resonance imaging (MRI).
D Situ, C W Reifel, R Smith, G W Lyons, R Temkin, C Harper-Little, S C Pang. J Anat 2002
9
50


A re-evaluation of the premaxillary bone in humans.
K Barteczko, M Jacob. Anat Embryol (Berl) 2004
33
50


The midline craniofacial skeleton in holoprosencephalic fetuses.
I Kjaer, J W Keeling, N Graem. J Med Genet 1991
45
50

Density of the alveolar and basal bones of the maxilla and the mandible.
Hyo-Sang Park, Youn-Ju Lee, Seong-Hwa Jeong, Tae-Geon Kwon. Am J Orthod Dentofacial Orthop 2008
140
50

The oral manifestations of cyclopia.
D G Gardner, H Lim. Oral Surg Oral Med Oral Pathol 1971
5
50

Multiple roles of cholesterol in hedgehog protein biogenesis and signaling.
P A Beachy, M K Cooper, K E Young, D P von Kessler, W J Park, T M Hall, D J Leahy, J A Porter. Cold Spring Harb Symp Quant Biol 1997
96
50

Cyclopia: a radiological and anatomical craniofacial post mortem study.
Claudio Cannistr, Patrick Barbet, Pasquale Parisi, Giorgio Iannetti. J Maxillofac Surg 2001
9
50

The cloverleaf skull anomaly: an anatomic and histologic study of two specimens.
V G Kokich, B C Moffett, M M Cohen. Cleft Palate J 1982
28
50

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
E Belloni, M Muenke, E Roessler, G Traverso, J Siegel-Bartelt, A Frumkin, H F Mitchell, H Donis-Keller, C Helms, A V Hing,[...]. Nat Genet 1996
487
50

Syndromes associated with holoprosencephaly.
Paul Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
25
50

Molecular cloning and characterization of a novel phospholipase C, PLC-eta.
Jong-Ik Hwang, Yong-Seok Oh, Kum-Joo Shin, Hyun Kim, Sung Ho Ryu, Pann-Ghill Suh. Biochem J 2005
79
50

Phospholipase C-eta enzymes as putative protein kinase C and Ca2+ signalling components in neuronal and neuroendocrine tissues.
Alan J Stewart, Kevin Morgan, Colin Farquharson, Robert P Millar. Neuroendocrinology 2007
29
50


Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog.
Benjamin D Solomon, Kelly A Bear, Adrian Wyllie, Amelia A Keaton, Christele Dubourg, Veronique David, Sandra Mercier, Sylvie Odent, Ute Hehr, Aimee Paulussen,[...]. J Med Genet 2012
51
50

Hereditary chronic pancreatitis.
Jonas Rosendahl, Hans Bödeker, Joachim Mössner, Niels Teich. Orphanet J Rare Dis 2007
72
50

Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.
C Geoffrey Woods, James Cox, Kelly Springell, Daniel J Hampshire, Moin D Mohamed, Martin McKibbin, Rowena Stern, F Lucy Raymond, Richard Sandford, Saghira Malik Sharif,[...]. Am J Hum Genet 2006
178
50

Pseudotrisomy 13 syndrome: use of homozygosity mapping to target candidate genes.
Renate Marquis-Nicholson, Salim Aftimos, Fern Ashton, Jennifer M Love, Peter Stone, Jeannette McFarlane, Alice M George, Donald R Love. Gene 2011
5
50

Loss of Tgif function causes holoprosencephaly by disrupting the SHH signaling pathway.
Kenichiro Taniguchi, Anoush E Anderson, Ann E Sutherland, David Wotton. PLoS Genet 2012
57
50

Intracellular Calcium Mobilization Is Required for Sonic Hedgehog Signaling.
Dana Klatt Shaw, Derrick Gunther, Michael J Jurynec, Alexis A Chagovetz, Erin Ritchie, David Jonah Grunwald. Dev Cell 2018
12
50

High Intellectual Function in Individuals with Mutation-Positive Microform Holoprosencephaly.
B D Solomon, D E Pineda-Alvarez, A L Gropman, M J Willis, D W Hadley, M Muenke. Mol Syndromol 2012
12
50

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
50

Mechanisms of vertebrate embryo segmentation: Common themes in trunk and limb development.
Caroline J Sheeba, Raquel P Andrade, Isabel Palmeirim. Semin Cell Dev Biol 2016
11
50

A developmental and genetic classification for malformations of cortical development: update 2012.
A James Barkovich, Renzo Guerrini, Ruben I Kuzniecky, Graeme D Jackson, William B Dobyns. Brain 2012
515
50

Extracephalic manifestations of nonchromosomal, nonsyndromic holoprosencephaly.
Ariel F Martinez, Paul S Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
3
50

Transcriptional landscape of the prenatal human brain.
Jeremy A Miller, Song-Lin Ding, Susan M Sunkin, Kimberly A Smith, Lydia Ng, Aaron Szafer, Amanda Ebbert, Zackery L Riley, Joshua J Royall, Kaylynn Aiona,[...]. Nature 2014
634
50

Holoprosencephaly-polydactyly/pseudotrisomy 13: a presentation of two new cases and a review of the literature.
Sophia M Bous, Benjamin D Solomon, Luitgard Graul-Neumann, Heidemarie Neitzel, Emily E Hardisty, Maximilian Muenke. Clin Dysmorphol 2012
9
50

Duplication of the ZIC2 gene is not associated with holoprosencephaly.
Vaidehi Jobanputra, Alanna Burke, Anyane-Yeboa Kwame, Anita Shanmugham, Maryam Shirazi, Stephen Brown, Peter E Warburton, Brynn Levy, Dorothy Warburton. Am J Med Genet A 2012
7
50

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
50

Proteomics of Primary Cilia by Proximity Labeling.
David U Mick, Rachel B Rodrigues, Ryan D Leib, Christopher M Adams, Allis S Chien, Steven P Gygi, Maxence V Nachury. Dev Cell 2015
199
50


Fetal ethanol exposure activates protein kinase A and impairs Shh expression in prechordal mesendoderm cells in the pathogenesis of holoprosencephaly.
Kazushi Aoto, Yayoi Shikata, Daisuke Higashiyama, Kohei Shiota, Jun Motoyama. Birth Defects Res A Clin Mol Teratol 2008
76
50

Functional SNP allele discovery (fSNPd): an approach to find highly penetrant, environmental-triggered genotypes underlying complex human phenotypes.
Kaitlin Stouffer, Michael Nahorski, Pablo Moreno, Nivedita Sarveswaran, David Menon, Michael Lee, C Geoffrey Woods. BMC Genomics 2017
3
50


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.