A citation-based method for searching scientific literature

Ilaria Fantasia, Rossana Bussani, Massimo Gregori, Floriana Zennaro, Giuseppina D'Ottavio, Lorenzo Monasta, Caterina Cortivo, Mariachiara Quadrifoglio, Gianpaolo Maso, Giuseppe Ricci, Chiara Ottaviani, Roberto Militello, Tamara Stampalija. Eur J Obstet Gynecol Reprod Biol 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Prenatal diagnosis of central nervous system abnormalities: Neurosonography versus fetal magnetic resonance imaging.
Atakan Tanacan, Burce Ozgen, Erdem Fadiloglu, Canan Unal, Kader Karli Oguz, Mehmet Sinan Beksac. Eur J Obstet Gynecol Reprod Biol 2020
4
50

Contribution of fetal brain MRI in management of severe fetal anemia.
L Ghesquière, V Houfflin-Debarge, P Verpillat, T Fourquet, S Joriot, C Coulon, P Vaast, C Garabedian. Eur J Obstet Gynecol Reprod Biol 2018
4
50

Fetal brain imaging: a comparison between magnetic resonance imaging and dedicated neurosonography.
G Malinger, L Ben-Sira, D Lev, Z Ben-Aroya, D Kidron, T Lerman-Sagie. Ultrasound Obstet Gynecol 2004
115
50

Prenatal and postnatal MRI findings in open spinal dysraphism following intrauterine repair via open versus fetoscopic surgical techniques.
Usha D Nagaraj, Karin S Bierbrauer, Charles B Stevenson, Jose L Peiro, Foong Yen Lim, Mounira A Habli, Beth M Kline-Fath. Prenat Diagn 2020
6
50

Cerebro-oculo-facio-skeletal syndrome.
Hiroshi Suzumura, Osamu Arisaka. Adv Exp Med Biol 2010
12
50

Prenatal diagnosis of the cerebro-oculo-facio-skeletal (COFS) syndrome.
D Paladini, M D'Armiento, I Ardovino, P Martinelli. Ultrasound Obstet Gynecol 2000
11
50

Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
J M Graham , K Anyane-Yeboa, A Raams, E Appeldoorn, W J Kleijer, V H Garritsen, D Busch, T G Edersheim, N G Jaspers. Am J Hum Genet 2001
85
50

First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure.
Nicolaas G J Jaspers, Anja Raams, Margherita Cirillo Silengo, Nils Wijgers, Laura J Niedernhofer, Andria Rasile Robinson, Giuseppina Giglia-Mari, Deborah Hoogstraten, Wim J Kleijer, Jan H J Hoeijmakers,[...]. Am J Hum Genet 2007
152
50

Heterogeneity and overlaps in nucleotide excision repair disorders.
Debora Ferri, Donata Orioli, Elena Botta. Clin Genet 2020
18
50

Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan.
Caroline Godfrey, Emma Clement, Rachael Mein, Martin Brockington, Janine Smith, Beril Talim, Volker Straub, Stephanie Robb, Ros Quinlivan, Lucy Feng,[...]. Brain 2007
268
50

Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stress.
Daniela T Soltys, Clarissa R R Rocha, Letícia K Lerner, Tiago A de Souza, Veridiana Munford, Fernanda Cabral, Tiziana Nardo, Miria Stefanini, Alain Sarasin, Januário B Cabral-Neto,[...]. Hum Mutat 2013
32
50


Pena-Shokeir phenotype (fetal akinesia deformation sequence) revisited.
Judith G Hall. Birth Defects Res A Clin Mol Teratol 2009
71
50

Smith-Lemli-Opitz syndrome: phenotype, natural history, and epidemiology.
Małgorzata J M Nowaczyk, Mira B Irons. Am J Med Genet C Semin Med Genet 2012
79
50

KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis.
Lucie Gueneau, Richard J Fish, Hanan E Shamseldin, Norine Voisin, Frédéric Tran Mau-Them, Egle Preiksaitiene, Glen R Monroe, Angeline Lai, Audrey Putoux, Fabienne Allias,[...]. Am J Hum Genet 2018
21
50

Fetal arthrogryposis: Challenges and perspectives for prenatal detection and management.
Isabel Filges, Sevgi Tercanli, Judith G Hall. Am J Med Genet C Semin Med Genet 2019
10
50

Normal development of the fetal brain by MRI.
Orit A Glenn. Semin Perinatol 2009
33
50

Prenatal diagnosis of cerebro-oculo-facio-skeletal syndrome: Report of three fetuses and review of the literature.
Pauline Le Van Quyen, Nadège Calmels, Maryse Bonnière, Suzanne Chartier, Féréchté Razavi, Jamel Chelly, Salima El Chehadeh, Sarah Baer, Lucile Boutaud, Séverine Bacrot,[...]. Am J Med Genet A 2020
2
50


A novel homozygous ERCC5 truncating mutation in a family with prenatal arthrogryposis--further evidence of genotype-phenotype correlation.
Suzanne Drury, Christopher Boustred, Mehmet Tekman, Horia Stanescu, Robert Kleta, Nicholas Lench, Lyn S Chitty, Richard H Scott. Am J Med Genet A 2014
23
50

Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report.
Rieko Sato, Jun-Ichi Takanashi, Yu Tsuyusaki, Mitsuhiro Kato, Hirotomo Saitsu, Naomichi Matsumoto, Takao Takahashi. Pediatrics 2016
7
50

Arthrogryposis.
Martha W F Rac, Jennifer McKinney, Manisha Gandhi. Am J Obstet Gynecol 2019
2
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.