A citation-based method for searching scientific literature

Octavian Munteanu, Monica Mihaela Cîrstoiu, Florin Mihail Filipoiu, Maria Narcisa Neamţu, Irina Stavarache, Tiberiu Augustin Georgescu, Ovidiu Gabriel Bratu, Gabriela Iorgulescu, Roxana Elena Bohîlţea. Rom J Morphol Embryol 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Morphological and ultrasonographic study of fetuses with cervical hygroma. A cases series.
Octavian Munteanu, Monica Mihaela Cîrstoiu, Florin Mihail Filipoiu, Roxana Elena BohîlŢea, Ioan Alexandru Bulescu, Costin Berceanu. Rom J Morphol Embryol 2016
9
50

New autoimmune diseases after cord blood transplantation: a retrospective study of EUROCORD and the Autoimmune Disease Working Party of the European Group for Blood and Marrow Transplantation.
Thomas Daikeler, Myriam Labopin, Annalisa Ruggeri, Alessandro Crotta, Mario Abinun, Ayad Ahmed Hussein, Kristina Carlson, Jérôme Cornillon, Jose L Diez-Martin, Virginie Gandemer,[...]. Blood 2013
53
25


Effects of long-term cryopreservation on hematopoietic progenitor cells in umbilical cord blood.
H Mugishima, K Harada, M Chin, T Suzuki, K Takagi, S Hayakawa, K Sato, J P Klein, R P Gale. Bone Marrow Transplant 1999
39
25

Ultrasound and MRI comprehensive approach in prenatal diagnosis of fetal osteochondrodysplasias. Cases series.
Costin Berceanu, Ioana Andreea Gheonea, Simona Vlădăreanu, Monica Mihaela Cîrstoiu, Radu Vlădăreanu, Claudia Mehedinţu, Sabina Berceanu, Răzvan Ciortea, Elvira Brătilă. Med Ultrason 2017
7
25

Cord blood banking for potential future transplantation.
Bertram H Lubin, William T Shearer. Pediatrics 2007
80
25


Length of cord blood unit cryopreservation does not impact hematopoietic engraftment.
Charlotte Jubert, Eric Wagner, Sonia Bizier, Marie-France Vachon, Michel Duval, Martin A Champagne. Transfusion 2008
3
33

Morphological study of cephalothoracopagus deradelphus type conjoined twins. A case report.
Monica Mihaela Cîrstoiu, Florin Mihail Filipoiu, Elvira Brătilă, Costin Berceanu, Florin Cătălin Cîrstoiu, Vlad Andrei Budu, Ioan Alexandru Bulescu, Octavian Munteanu. Rom J Morphol Embryol 2016
3
33

Maternal overweight and obesity and the risk of congenital anomalies: a systematic review and meta-analysis.
Katherine J Stothard, Peter W G Tennant, Ruth Bell, Judith Rankin. JAMA 2009
701
25

Body stalk anomaly in a monochorionic-diamniotic twin pregnancy - case report and review of the literature.
Roxana Elena Bohîlţea, Cicerone Florentin Tufan, Monica Mihaela Cîrstoiu, Adrian Vasile Dumitru, Tiberiu Augustin Georgescu, Maria Sajin, Oana Maria Bodean, Octavian Munteanu, Elvira Brătilă, Anca Maria Ofiţeru,[...]. Rom J Morphol Embryol 2017
7
25


Magnetic Resonance Imaging Evaluation of Fetal Neural Tube Defects.
Alexia Egloff, Dorothy Bulas. Semin Ultrasound CT MR 2015
15
25

Fetal evaluation of spine dysraphism.
Dorothy Bulas. Pediatr Radiol 2010
31
25

Recognition of caudal regression syndrome.
Mari M Boulas. Adv Neonatal Care 2009
22
25

Malformation risks of antiepileptic drugs in pregnancy: a prospective study from the UK Epilepsy and Pregnancy Register.
J Morrow, A Russell, E Guthrie, L Parsons, I Robertson, R Waddell, B Irwin, R C McGivern, P J Morrison, J Craig. J Neurol Neurosurg Psychiatry 2006
513
25

Sacrococcygeal teratoma in one twin: a case report and literature review.
Qing Hu, Yiyun Yan, Hua Liao, Hongyan Liu, Haiyan Yu, Fumin Zhao. BMC Pregnancy Childbirth 2020
3
33

Central nervous system malformations in a perinatal/neonatal autopsy series.
H Pinar, N Tatevosyants, D B Singer. Pediatr Dev Pathol 1998
47
25


Associated anomalies with neural tube defects in fetal autopsies.
Havva Serap Toru, Cem Yasar Sanhal, Özlem Ceren Uzun, Guzide Ayse Ocak, İnanç Mendilcioğlu, Fatma Şeyda Karaveli. J Matern Fetal Neonatal Med 2016
9
25

Caudal agenesis and associated caudal spinal cord malformations.
D Estin, A R Cohen. Neurosurg Clin N Am 1995
21
25


The sacrum: pathologic spectrum, multimodality imaging, and subspecialty approach.
J Diel, O Ortiz, R A Losada, D B Price, M W Hayt, D S Katz. Radiographics 2001
85
25

A systematic review of the risks factors associated with the onset and natural progression of spina bifida.
Jennifer Donnan, Stephanie Walsh, Lindsey Sikora, Andrea Morrissey, Kayla Collins, Don MacDonald. Neurotoxicology 2017
11
25

Development of the posterior neural tube in human embryos.
Hirotomo Saitsu, Shigehito Yamada, Chigako Uwabe, Makoto Ishibashi, Kohei Shiota. Anat Embryol (Berl) 2004
48
25

Current classification and imaging of congenital spinal abnormalities.
Andrea Rossi, Carlo Gandolfo, Giovanni Morana, Gianluca Piatelli, Marcello Ravegnani, Alessandro Consales, Marco Pavanello, Armando Cama, Paolo Tortori-Donati. Semin Roentgenol 2006
19
25

Walker-Warburg syndrome and tectocerebellar dysraphia: A novel association caused by a homozygous DAG1 mutation.
Zvi Leibovitz, Hanna Mandel, Tzipora C Falik-Zaccai, Shani Ben Harouch, David Savitzki, Karina Krajden-Haratz, Liat Gindes, Mordechai Tamarkin, Dorit Lev, William B Dobyns,[...]. Eur J Paediatr Neurol 2018
8
25

Septo-optic dysplasia.
Emma A Webb, Mehul T Dattani. Eur J Hum Genet 2010
133
25

Recurrent partial rhombencephalosynapsis and holoprosencephaly in siblings with a mutation of ZIC2.
Melissa B Ramocki, Fernando Scaglia, Pawel Stankiewicz, John W Belmont, Jeremy Y Jones, Gary D Clark. Am J Med Genet A 2011
16
25

Hydrocephalus in children.
Kristopher T Kahle, Abhaya V Kulkarni, David D Limbrick, Benjamin C Warf. Lancet 2016
248
25

Hydranencephaly: Clinical Features and Survivorship in a Retrospective Cohort.
Abdelsimar T Omar, Minette Krisel A Manalo, Ralph Rommualdo A Zuniega, John Carlo B Reyes, Edroico Mari B Brillante, Kathleen Joy O Khu. World Neurosurg 2020
1
100


Cortical Dysplasia and the mTOR Pathway: How the Study of Human Brain Tissue Has Led to Insights into Epileptogenesis.
Wei Shern Lee, Sara Baldassari, Sarah E M Stephenson, Paul J Lockhart, Stéphanie Baulac, Richard J Leventer. Int J Mol Sci 2022
3
33

Magnetic resonance imaging of the kinked fetal brain stem: a sign of severe dysgenesis.
Annemarie Stroustrup Smith, Deborah Levine, Patrick D Barnes, Richard L Robertson. J Ultrasound Med 2005
27
25

The Clinical and Molecular Characteristics of Molybdenum Cofactor Deficiency Due to MOCS2 Mutations.
Pinar Arican, Pinar Gencpinar, Ozgur Kirbiyik, Sema Bozkaya Yilmaz, Atilla Ersen, Ozgur Oztekin, Nihal Olgac Dundar. Pediatr Neurol 2019
9
25

Fetal schizencephaly: pre- and postnatal imaging with a review of the clinical manifestations.
Karen Y Oh, Anne M Kennedy, Antonio E Frias, Janice L B Byrne. Radiographics 2005
44
25

Clinical and Imaging Profile of Patients with Joubert Syndrome.
Bharath Kumar Surisetti, Vikram Venkappayya Holla, Shweta Prasad, Koti Neeraja, Nitish Kamble, Ravi Yadav, Pramod Kumar Pal. J Mov Disord 2021
3
33

Functional Connectivity and Genetic Profile of a "Double-Cortex"-Like Malformation.
Giulia Sprugnoli, Giampaolo Vatti, Simone Rossi, Alfonso Cerase, Alessandra Renieri, Maria A Mencarelli, Federico Zara, Alessandro Rossi, Emiliano Santarnecchi. Front Integr Neurosci 2018
3
33

Recent advances in understanding inheritance of holoprosencephaly.
Christèle Dubourg, Artem Kim, Erwan Watrin, Marie de Tayrac, Sylvie Odent, Véronique David, Valérie Dupé. Am J Med Genet C Semin Med Genet 2018
27
25

Sporadic COL4A1 mutations with extensive prenatal porencephaly resembling hydranencephaly.
M E C Meuwissen, L S de Vries, H A Verbeek, M H Lequin, P P Govaert, R Schot, F M Cowan, R Hennekam, P Rizzu, F W Verheijen,[...]. Neurology 2011
41
25

Prenatal diagnosis of middle interhemispheric variant of holoprosencephaly: review of literature and prenatal case series.
Ine Tavano, Bart De Keersmaecker, Michael Aertsen, Luc De Catte. J Matern Fetal Neonatal Med 2022
2
50

Septopreoptic holoprosencephaly: a mild subtype associated with midline craniofacial anomalies.
J S Hahn, P D Barnes, N J Clegg, E E Stashinko. AJNR Am J Neuroradiol 2010
35
25

Children with agenesis of the corpus callosum.
J L Grogono. Dev Med Child Neurol 1968
80
25

Joubert syndrome and related disorders.
Enza Maria Valente, Bruno Dallapiccola, Enrico Bertini. Handb Clin Neurol 2013
52
25


Holoprosencephaly from conception to adulthood.
Karin Weiss, Paul S Kruszka, Eric Levey, Max Muenke. Am J Med Genet C Semin Med Genet 2018
9
25

EML1-associated brain overgrowth syndrome with ribbon-like heterotopia.
Renske Oegema, George McGillivray, Richard Leventer, Anne-Gaëlle Le Moing, Nadia Bahi-Buisson, Angela Barnicoat, Simone Mandelstam, David Francis, Fiona Francis, Grazia M S Mancini,[...]. Am J Med Genet C Semin Med Genet 2019
14
25

Neuroimaging of pediatric central nervous system cytomegalovirus infection.
Kathleen R Fink, Mahesh M Thapa, Gisele E Ishak, Sumit Pruthi. Radiographics 2010
62
25

Lissencephaly: Expanded imaging and clinical classification.
Nataliya Di Donato, Sara Chiari, Ghayda M Mirzaa, Kimberly Aldinger, Elena Parrini, Carissa Olds, A James Barkovich, Renzo Guerrini, William B Dobyns. Am J Med Genet A 2017
60
25

Rhombencephalosynapsis: Fused cerebellum, confused geneticists.
Kimberly A Aldinger, Jennifer C Dempsey, Hannah M Tully, Megan E Grout, Michele G Mehaffey, William B Dobyns, Dan Doherty. Am J Med Genet C Semin Med Genet 2018
20
25


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.