A citation-based method for searching scientific literature

Tommy Hu, Paul Kruszka, Ariel F Martinez, Jeffrey E Ming, Emily K Shabason, Manu S Raam, Tamim H Shaikh, Daniel E Pineda-Alvarez, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Syndromes associated with holoprosencephaly.
Paul Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
22
50

Use of MRI in the diagnosis of fetal brain abnormalities in utero (MERIDIAN): a multicentre, prospective cohort study.
Paul D Griffiths, Michael Bradburn, Michael J Campbell, Cindy L Cooper, Ruth Graham, Deborah Jarvis, Mark D Kilby, Gerald Mason, Cara Mooney, Stephen C Robson,[...]. Lancet 2017
113
50

A survey of fetal care centers in the United States.
J C Kett, D E Woodrum, D S Diekema. J Neonatal Perinatal Med 2014
11
50

Fast MR imaging of fetal central nervous system abnormalities.
Deborah Levine, Patrick D Barnes, Richard R Robertson, Geoffrey Wong, Tejas S Mehta. Radiology 2003
131
50

Holoprosencephaly: recommendations for diagnosis and management.
Emily F Kauvar, Maximilian Muenke. Curr Opin Pediatr 2010
28
50

The Dandy-Walker variant: a case series of 24 pediatric patients and evaluation of associated anomalies, incidence of hydrocephalus, and developmental outcomes.
Deanna Sasaki-Adams, Samer K Elbabaa, Valerie Jewells, Lori Carter, Jeffrey W Campbell, Ann M Ritter. J Neurosurg Pediatr 2008
38
50


A Neuropsychological Profile for Agenesis of the Corpus Callosum? Cognitive, Academic, Executive, Social, and Behavioral Functioning in School-Age Children.
Vanessa Siffredi, Vicki Anderson, Alissandra McIlroy, Amanda G Wood, Richard J Leventer, Megan M Spencer-Smith. J Int Neuropsychol Soc 2018
11
50

Neuropsychological profile of agenesis of the corpus callosum: a systematic review.
Vanessa Siffredi, Vicki Anderson, Richard J Leventer, Megan M Spencer-Smith. Dev Neuropsychol 2013
47
50

Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis.
Francesco D'Antonio, Giorgio Pagani, Alessandra Familiari, Asma Khalil, Tally-Lerman Sagies, Gustavo Malinger, Zvi Leibovitz, Catherine Garel, Marie Laure Moutard, Gianluigi Pilu,[...]. Pediatrics 2016
55
50

Genetic Syndromes Associated with Congenital Cardiac Defects and Ophthalmologic Changes - Systematization for Diagnosis in the Clinical Practice.
Priscila H A Oliveira, Beatriz S Souza, Eimi N Pacheco, Michele S Menegazzo, Ivan S Corrêa, Paulo R G Zen, Rafael F M Rosa, Claudia C Cesa, Lucia C Pellanda, Manuel A P Vilela. Arq Bras Cardiol 2018
5
50

Holoprosencephaly: antenatal and postnatal diagnosis and outcome.
Chandrasekaran Kaliaperumal, Sam Ndoro, Tafadzwa Mandiwanza, F Reidy, F McAuliffe, John Caird, Darach Crimmins. Childs Nerv Syst 2016
8
50

The Contribution of MRI after Fetal Anomalies Have Been Diagnosed by Ultrasound: Correlation with Postnatal Outcomes.
Bero Verburg, A Michelle Fink, Karen Reidy, Ricardo Palma-Dias. Fetal Diagn Ther 2015
12
50


Holoprosencephaly due to numeric chromosome abnormalities.
Benjamin D Solomon, Kenneth N Rosenbaum, Jeanne M Meck, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
40
50

MLPA screening reveals novel subtelomeric rearrangements in holoprosencephaly.
Claude Bendavid, Christèle Dubourg, Laurent Pasquier, Isabelle Gicquel, Simon Le Gallou, Stéphanie Mottier, Marie-Renée Durou, Catherine Henry, Sylvie Odent, Véronique David. Hum Mutat 2007
21
50

Epidemiology of holoprosencephaly in Hawaii, 1986-97.
M B Forrester, R D Merz. Paediatr Perinat Epidemiol 2000
17
50

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
219
50

Phenotypic variability in human embryonic holoprosencephaly in the Kyoto Collection.
Shigehito Yamada, Chigako Uwabe, Shingo Fujii, Kohei Shiota. Birth Defects Res A Clin Mol Teratol 2004
63
50


Cerebral midline developmental anomalies: spectrum and associated features.
A L Delezoide, F Narcy, J C Larroche. Genet Couns 1990
12
50

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
Christèle Dubourg, Leïla Lazaro, Laurent Pasquier, Claude Bendavid, Martine Blayau, Franck Le Duff, Marie-Renée Durou, Sylvie Odent, Véronique David. Hum Mutat 2004
114
50

Holoprosencephaly and trisomy 21 in a child born to a nondiabetic mother.
M Urioste, E Valcarcel, M A Gomez, I Pinel, R Garcia de León, A Diaz de Bustamante, R Tebar, M L Martinez-Frias. Am J Med Genet 1988
29
50

Prenatal diagnosis of triploidy associated with holoprosencephaly: a case report and review of the literature.
Gharid N Bekdache, Muzib Begam, Walaa Al Safi, Hisham Mirghani. Am J Perinatol 2009
6
50

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
63
50

Epidemiology of holoprosencephaly: Prevalence and risk factors.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
60
50


Holoprosencephaly: birth data, benetic and demographic analyses of 30 families.
E Roach, W Demyer, P M Conneally, C Palmer, A D Merritt. Birth Defects Orig Artic Ser 1975
105
50

Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
40
50

Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci.
Claude Bendavid, Lucie Rochard, Christèle Dubourg, Jonathan Seguin, Isabelle Gicquel, Laurent Pasquier, Jaqueline Vigneron, Annie Laquerrière, Pascale Marcorelles, Corinne Jeanne-Pasquier,[...]. Hum Mutat 2009
35
50

Holoprosencephaly in hungary: birth prevalence and clinical spectrum.
Nóra Szabó, Gyurgyinka Gergev, Jeno Kóbor, Péter Szucs, Sándor Túri, László Sztriha. J Child Neurol 2011
5
50

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
62
50

Disorders of prosencephalic development.
P Volpe, G Campobasso, V De Robertis, G Rembouskos. Prenat Diagn 2009
49
50



An epidemiological study of holoprosencephaly from a regional congenital anomaly register: 1995-2004.
S Ong, A Tonks, E R Woodward, M P Wyldes, M D Kilby. Prenat Diagn 2007
30
50

Holoprosencephaly in the west of Scotland 1975-1994.
M L Whiteford, J L Tolmie. J Med Genet 1996
37
50

Clinical epidemiologic study of holoprosencephaly in South America.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet A 2007
36
50

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
839
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.