A citation-based method for searching scientific literature

Sara H El-Dessouky, Mona M Aboulghar, Hassan M Gaafar, Rana M Abdella, Marwa F Sharaf, Mohamed I Ateya, Ahmed Ezz Elarab, Walaa H Zidan, Rania M Helal, Samah M Aboelsaud, Maha M Eid, Ghada M H Abdel-Salam. Prenat Diagn 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Prenatal ultrasound diagnosis in 51 cases of holoprosencephaly: craniofacial anatomy, associated malformations, and genetics.
M Wenghoefer, Anke M Ettema, F Sina, A Geipel, A M Kuijpers-Jagtman, H Hansmann, W A Borstlap, S Bergé. Cleft Palate Craniofac J 2010
8
50

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
50

Holoprosencephaly at prenatal diagnosis: analysis of 28 cases regarding etiopathogenic diagnoses.
F Petracchi, L Crespo, C Michia, L Igarzabal, E Gadow. Prenat Diagn 2011
11
25

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
25

The 11-13-week scan: diagnosis and outcome of holoprosencephaly, exomphalos and megacystis.
K O Kagan, I Staboulidou, A Syngelaki, J Cruz, K H Nicolaides. Ultrasound Obstet Gynecol 2010
48
25

Clinical epidemiologic study of holoprosencephaly in South America.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet A 2007
36
25

The wide spectrum of ultrasound diagnosis of holoprosencephaly.
Cringu Antoniu Ionescu, Simona Vladareanu, Stefania Tudorache, Liana Ples, Catalin Herghelegiu, Adrian Neacsu, Dan Navolan, Ioana Dragan, Daniela Nuti Oprescu. Med Ultrason 2019
6
25

Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
43
25

Holoprosencephaly spectrum among Egyptian patients: clinical and cytogenetic study.
H T El-Bassyouni, G H Abdel Salam, S N Saleem, H F Kayed, M I Shehab, M M Eid, M E Zaki, M S Zaki. Genet Couns 2014
2
50


Are the prevalence of Trisomy 13 and the incidence of severe holoprosencephaly increasing in Africa?
Jude Ogechukwu Okoye, Anthony Ajuluchukwu Ngokere. Prenat Diagn 2020
1
100

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
41
25

Recurrent triploidy of maternal origin.
Francesco Brancati, Rita Mingarelli, Bruno Dallapiccola. Eur J Hum Genet 2003
22
25

Detection of triploidy at 11-14 weeks' gestation: a cohort study of 198 000 pregnant women.
L Engelbrechtsen, K Brøndum-Nielsen, C Ekelund, A Tabor, L Skibsted. Ultrasound Obstet Gynecol 2013
20
25

Pathogenesis of holoprosencephaly.
Xin Geng, Guillermo Oliver. J Clin Invest 2009
59
25

What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
25

Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy.
Milenko Kolarski, Begzudin Ahmetovic, Maja Beres, Radomir Topic, Vedran Nikic, Ivana Kavecan, Semin Sabic. Med Arch 2017
3
33

Multidisciplinary team approach to the prenatal management of orofacial clefts: a single center cohort study in Taiwan.
Hsuan Ko, Tung-Yao Chang, Eric C Lussier, Ksenia Olisova, Chan-Yu Sung, Philip Kuo-Ting Chen, Wen-Chu Li, Tze-Yi Yang, Ru-Xuan Wang. Sci Rep 2020
1
100


Second-trimester fetal autopsy: A morphological study with prenatal USG correlations and clinical implications.
Chaitra Venkataswamy, Umamaheswari Gurusamy, S Vidhya Lakshmi. J Lab Physicians 2018
2
50

Hydrocephalic holoprosencephaly: An oxymoron? Insights into etiology and management.
Anuj Kumar Tripathi, Deepak Agrawal, Gopal Sedain. J Pediatr Neurosci 2009
3
33

Holoprosencephaly: a guide to diagnosis and clinical management.
Manu S Raam, Benjamin D Solomon, Maximilian Muenke. Indian Pediatr 2011
22
25

Decision-making after ultrasound diagnosis of fetal abnormality.
Hilmar H Bijma, Agnes van der Heide, Hajo I J Wildschut. Reprod Health Matters 2008
36
25

Triploidy in a twin pregnancy: small placenta volume as an early sonographical marker.
Rainer Gassner, Martin Metzenbauer, Erich Hafner, Ursula Vallazza, Karl Philipp. Prenat Diagn 2003
12
25

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
25

Placental pathology of triploidy.
D E McFadden, J T Pantzar. Hum Pathol 1996
25
25

Prenatal diagnosis of fetal aneuploidies using QF-PCR: the egyptian study.
Shereen H Atef, Sawsan S Hafez, Nermein H Mahmoud, Sanaa M Helmy. J Prenat Med 2011
6
25

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

The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes.
Aimée D C Paulussen, Constance T Schrander-Stumpel, Demis C J Tserpelis, Matteus K M Spee, Alexander P A Stegmann, Grazia M Mancini, Alice S Brooks, Margriet Collée, Anneke Maat-Kievit, Marleen E H Simon,[...]. Eur J Hum Genet 2010
32
25

Assessment of QF-PCR as the first approach in prenatal diagnosis.
Celia Badenas, Laia Rodríguez-Revenga, Carme Morales, Carmen Mediano, Alberto Plaja, Ma Mar Pérez-Iribarne, Anna Soler, Núria Clusellas, Antoni Borrell, Ma Ángeles Sánchez,[...]. J Mol Diagn 2010
30
25

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
25

Holoprosencephaly: prenatal sonographic diagnosis.
D A Nyberg, L A Mack, A Bronstein, J Hirsch, R A Pagon. AJR Am J Roentgenol 1987
48
25

Genome-wide abnormalities in embryos: Origins and clinical consequences.
Heleen Masset, Olga Tšuiko, Joris R Vermeesch. Prenat Diagn 2021
1
100

"Double trouble" or an amplification of the triploidy phenotype?
Kathrin Ludwig, Marco Pizzi, Matteo Fassan, Cecilia Daolio, Katia Margiotti, Federica Consoli, Roberto Salmaso, Massimo Rugge. Fetal Pediatr Pathol 2013
2
50

Triploidy: Variation of Phenotype.
M Hassan Toufaily, Drucilla J Roberts, Marie-Noel Westgate, Lewis B Holmes. Am J Clin Pathol 2016
19
25

A genetic review of complete and partial hydatidiform moles and nonmolar triploidy.
N M Lindor, J A Ney, T A Gaffey, R B Jenkins, S N Thibodeau, G W Dewald. Mayo Clin Proc 1992
42
25

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
25

Alobar holoprosencephaly associated with a rare chromosomal abnormality: Case report and literature review.
Crîngu Antoniu Ionescu, Dan Calin, Dan Navolan, Alexandra Matei, Mihai Dimitriu, Catalin Herghelegiu, Liana Ples. Medicine (Baltimore) 2018
4
25

Digynic triploidy in a fetus presenting with semilobar holoprosencephaly.
Tzu-Yun Chuang, Shu-Yuan Chang, Chih-Ping Chen, Ming-Huei Lin, Cheng-Yu Chen, Shin-Wen Chen, Schu-Rern Chern, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang. Taiwan J Obstet Gynecol 2018
2
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
33

Alobar holoprosencephaly and Trisomy 13 (Patau syndrome).
Andressa Dias Costa, Regina Schultz, Sérgio Rosemberg. Autops Case Rep 2013
1
100

The crucial role of SRY gene in the determination of human genetic sex: 46,XX disorder of sex development.
Cristina Crenguţa Albu, Dinu Florin Albu, Ana Roxana Muşat, Ioana Georgeta Stancu, Ştefan Dimitrie Albu, Anca Pătraşcu, Alexandru Marian Gogănău. Rom J Morphol Embryol 2019
3
33

Prenatal ultrasound diagnosis of holoprosencephaly and associated anomalies.
Hemang D Chaudhari, Gurudatt Thakkar, Parth Darji, Pratik Khokhani. BMJ Case Rep 2012
5
25

Antenatal diagnosis of alobar holoprosencephaly.
Rajesh Raman, Geetha Mukunda Jagadesh. Case Rep Radiol 2014
5
25

Morphologic anomalies in triploid liveborn fetuses.
N Doshi, U Surti, A E Szulman. Hum Pathol 1983
82
25

Ultrasound diagnosis in two cases of severe craniofacial anomalies.
Mirela Ritivoiu, Florin Brezan, Ioana Codreanu, Mircea Stamate, Ioana Anca. Med Ultrason 2013
1
100


Prenatal sonographic features of triploidy at 12-16 weeks.
Yaron Zalel, Israel Shapiro, Alina Weissmann-Brenner, Michal Berkenstadt, Zvi Leibovitz, Moshe Bronshtein. Prenat Diagn 2016
14
25

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
25

Impact of genetic testing and family health history of cystic fibrosis in the early prenatal diagnosis and prevention of a new case of genetic disorder.
Cristina Crenguţa Albu, Ioana Georgeta Stancu, Liliana Georgiana Grigore, Dinu Florin Albu, Ştefan Dimitrie Albu, Anca Pătraşcu, Alexandru Marian Gogănău. Rom J Morphol Embryol 2019
1
100


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.