A citation-based method for searching scientific literature

Carlo Bellini, Gloria Donarini, Dario Paladini, Maria Grazia Calevo, Tommaso Bellini, Luca A Ramenghi, Raoul C Hennekam. Am J Med Genet A 2015
Times Cited: 71







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



Times Cited
  Times     Co-cited
Similarity


Society for maternal-fetal medicine (SMFM) clinical guideline #7: nonimmune hydrops fetalis.
Mary E Norton, Suneet P Chauhan, Jodi S Dashe. Am J Obstet Gynecol 2015
91
35

Prenatal diagnosis of non-immune hydrops fetalis: what do we tell the parents?
Susana Santo, Sahar Mansour, Basky Thilaganathan, Tessa Homfray, Aris Papageorghiou, Sandra Calvert, Amar Bhide. Prenat Diagn 2011
56
33

Etiology of nonimmune hydrops fetalis: a systematic review.
Carlo Bellini, Raoul C M Hennekam, Ezio Fulcheri, Mariangela Rutigliani, Guido Morcaldi, Francesco Boccardo, Eugenio Bonioli. Am J Med Genet A 2009
99
25


Lysosomal storage disease as an etiology of nonimmune hydrops.
Alexis C Gimovsky, Paola Luzi, Vincenzo Berghella. Am J Obstet Gynecol 2015
33
42

Nonimmune hydrops fetalis: identifying the underlying genetic etiology.
Teresa N Sparks, Kao Thao, Billie R Lianoglou, Nina M Boe, Kari G Bruce, Ilina Datkhaeva, Nancy T Field, Victoria M Fratto, Jennifer Jolley, Louise C Laurent,[...]. Genet Med 2019
19
73

Non-immune hydrops fetalis: a short review of etiology and pathophysiology.
Carlo Bellini, Raoul C M Hennekam. Am J Med Genet A 2012
74
18

Investigation of lysosomal storage diseases in nonimmune hydrops fetalis.
Maira G Burin, Ana P Scholz, Rejane Gus, Maria Teresa V Sanseverino, Alessandra Fritsh, José A Magalhães, Fernanda Timm, Patrícia Barrios, Marisa Chesky, Janice C Coelho,[...]. Prenat Diagn 2004
57
22

Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.
Elisavet Fotiou, Silvia Martin-Almedina, Michael A Simpson, Shin Lin, Kristiana Gordon, Glen Brice, Giles Atton, Iona Jeffery, David C Rees, Cyril Mignot,[...]. Nat Commun 2015
136
18

Perinatal and one-year outcomes of non-immune hydrops fetalis by etiology and age at diagnosis.
Shiyo Ota, Jun Sahara, Aki Mabuchi, Ryo Yamamoto, Keisuke Ishii, Nobuaki Mitsuda. J Obstet Gynaecol Res 2016
23
56

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
18

Short-term and long-term outcomes of 214 cases of non-immune hydrops fetalis.
Kotaro Fukushima, Seiichi Morokuma, Yasuyuki Fujita, Kiyomi Tsukimori, Shoji Satoh, Masayuki Ochiai, Toshiro Hara, Tomoaki Taguchi, Norio Wake. Early Hum Dev 2011
36
33

Non-immune hydrops fetalis: A prospective study of 53 cases.
Carolina A Moreno, Thatiane Kanazawa, Ricardo Barini, Marcelo L Nomura, Kléber C Andrade, Cristiane P Gomes, Juliana K Heinrich, Roberto Giugliani, Maira Burin, Denise P Cavalcanti. Am J Med Genet A 2013
24
50

Analysis of outcome in hydrops fetalis in relation to gestational age at diagnosis, cause and treatment.
K Sohan, S G Carroll, S De La Fuente, P Soothill, P Kyle. Acta Obstet Gynecol Scand 2001
54
22

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
163
14


Etiology and outcome of hydrops fetalis: report of 62 cases.
Sahin Takci, Mina Gharibzadeh, Murat Yurdakok, Ozgur Ozyuncu, Ayse Korkmaz, Zuhal Akcoren, Sule Yigit. Pediatr Neonatol 2014
18
50

The many faces of hydrops.
S Christopher Derderian, Cerine Jeanty, Shannon R Fleck, Lily S Cheng, Shabnam Peyvandi, Anita J Moon-Grady, Jody Farrell, Shinjiro Hirose, Juan Gonzalez, Roberta L Keller,[...]. J Pediatr Surg 2015
21
42

Lysosomal storage disorder in non-immunological hydrops fetalis (NIHF): more common than assumed? Report of four cases with transient NIHF and a review of the literature.
Catharina Whybra, Eugen Mengel, Alexandra Russo, Franz Bahlmann, Christoph Kampmann, Michael Beck, Elke Eich, Eva Mildenberger. Orphanet J Rare Dis 2012
32
28

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
127
12

A system-based approach to the genetic etiologies of non-immune hydrops fetalis.
Anne H Mardy, Shilpa P Chetty, Mary E Norton, Teresa N Sparks. Prenat Diagn 2019
17
52

Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans.
Marielle Alders, Benjamin M Hogan, Evisa Gjini, Faranak Salehi, Lihadh Al-Gazali, Eric A Hennekam, Eva E Holmberg, Marcel M A M Mannens, Margot F Mulder, G Johan A Offerhaus,[...]. Nat Genet 2009
182
9

Prognostic factors and clinical features in liveborn neonates with hydrops fetalis.
Hsuan-Rong Huang, Pei-Kwei Tsay, Ming-Chou Chiang, Reyin Lien, Yi-Hung Chou. Am J Perinatol 2007
35
20

EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.
Silvia Martin-Almedina, Ines Martinez-Corral, Rita Holdhus, Andres Vicente, Elisavet Fotiou, Shin Lin, Kjell Petersen, Michael A Simpson, Alexander Hoischen, Christian Gilissen,[...]. J Clin Invest 2016
46
15

Epidemiology of Live Born Infants with Nonimmune Hydrops Fetalis-Insights from a Population-Based Dataset.
Martina A Steurer, Shabnam Peyvandi, Rebecca J Baer, Tippi MacKenzie, Ben C Li, Mary E Norton, Laura L Jelliffe-Pawlowski, Anita J Moon-Grady. J Pediatr 2017
14
50

Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development.
Carin L Yates, Kristin G Monaghan, Deborah Copenheaver, Kyle Retterer, Julie Scuffins, Cathlin R Kucera, Bethany Friedman, Gabriele Richard, Jane Juusola. Genet Med 2017
65
10

Metabolic causes of nonimmune hydrops fetalis: A next-generation sequencing panel as a first-line investigation.
Bénédicte Sudrié-Arnaud, Florent Marguet, Sophie Patrier, Jelena Martinovic, Ferielle Louillet, Françoise Broux, Françoise Charbonnier, Hélène Dranguet, Sophie Coutant, Myriam Vezain,[...]. Clin Chim Acta 2018
23
30

Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome.
Mariëlle Alders, Lihadh Al-Gazali, Isabelle Cordeiro, Bruno Dallapiccola, Livia Garavelli, Beyhan Tuysuz, Faranak Salehi, Martin A Haagmans, Olaf R Mook, Charles B Majoie,[...]. Hum Genet 2014
74
8

Lysosomal storage diseases in non-immune hydrops fetalis pregnancies.
Angelique J A Kooper, Pim M W Janssens, Akosua N J A de Groot, Maria L F Liebrand-van Sambeek, Catharina J M G van den Berg, Gita B Tan-Sindhunata, Paul P van den Berg, Emilia K Bijlsma, Arie P T Smits, Ron A Wevers. Clin Chim Acta 2006
30
20

Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia.
Viktor Lukacs, Jayanti Mathur, Rong Mao, Pinar Bayrak-Toydemir, Melinda Procter, Stuart M Cahalan, Helen J Kim, Michael Bandell, Nicola Longo, Ronald W Day,[...]. Nat Commun 2015
125
8

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
657
8


Outcome and Treatment of Antenatally Diagnosed Nonimmune Hydrops Fetalis.
Ahmed A Nassr, Amen Ness, Pardis Hosseinzadeh, Bahram Salmanian, Jimmy Espinoza, Victoria Berger, Eleonore Werner, Hadi Erfani, Stephen Welty, Zhoobin H Bateni,[...]. Fetal Diagn Ther 2018
12
50

Nonimmunologic hydrops fetalis: a review of 61 cases.
A A Hutchison, J H Drew, V Y Yu, M L Williams, D W Fortune, N A Beischer. Obstet Gynecol 1982
202
8

Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.
Fiona Connell, Kamini Kalidas, Pia Ostergaard, Glen Brice, Tessa Homfray, Lesley Roberts, David J Bunyan, Sally Mitton, Sahar Mansour, Peter Mortimer,[...]. Hum Genet 2010
63
7


Nonimmune hydrops fetalis diagnosed during the second half of pregnancy in Southern China.
Can Liao, Jiaxue Wei, Qiuming Li, Jian Li, Lixian Li, Dongzhi Li. Fetal Diagn Ther 2007
42
11

Fast protocol for the diagnosis of lysosomal diseases in nonimmune hydrops fetalis.
Laura Gort, M Reyes Granell, Gema Fernández, Práxedes Carreto, Aurora Sanchez, M José Coll. Prenat Diagn 2012
23
21


Long-term in utero drainage of fetal hydrothorax.
C H Rodeck, N M Fisk, D I Fraser, U Nicolini. N Engl J Med 1988
140
7

Clinical characteristics and perinatal outcome of fetal hydrops.
Wonkyung Yeom, E Sun Paik, Jung-Joo An, Soo-Young Oh, Suk-Joo Choi, Cheong-Rae Roh, Jong-Hwa Kim. Obstet Gynecol Sci 2015
13
38

Lysosomal Storage Disorders in Nonimmune Hydrops Fetalis (NIHF): An Indian Experience.
Jayesh Sheth, Mehul Mistri, Krati Shah, Mayank Chaudhary, Koumudi Godbole, Frenny Sheth. JIMD Rep 2017
9
55

Preeclampsia due to fetal non-immune hydrops: mirror syndrome and review of literature.
Ali Gedikbasi, Kazim Oztarhan, Ziya Gunenc, Gokhan Yildirim, Oguz Arslan, Dogukan Yildirim, Yavuz Ceylan. Hypertens Pregnancy 2011
21
23

Molecular autopsy in maternal-fetal medicine.
Hanan E Shamseldin, Wesam Kurdi, Fatima Almusafri, Maha Alnemer, Alya Alkaff, Zeneb Babay, Amal Alhashem, Maha Tulbah, Nada Alsahan, Rubina Khan,[...]. Genet Med 2018
49
10

Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalis.
Ilina Datkhaeva, Valerie A Arboleda, T Niroshi Senaratne, Gelareh Nikpour, Cherise Meyerson, Yipeng Geng, Yalda Afshar, Emily Scibetta, Jeffrey Goldstein, Fabiola Quintero-Rivera,[...]. Am J Med Genet A 2018
16
31

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
Teresa N Sparks, Billie R Lianoglou, Rebecca R Adami, Ilina D Pluym, Kerry Holliman, Jennifer Duffy, Sarah L Downum, Sachi Patel, Amanda Faubel, Nina M Boe,[...]. N Engl J Med 2020
23
21

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.
F C Connell, K Gordon, G Brice, V Keeley, S Jeffery, P S Mortimer, S Mansour, P Ostergaard. Clin Genet 2013
81
5

A cardiovascular profile score in the surveillance of fetal hydrops.
Cornelia Hofstaetter, Manfred Hansmann, Sturla H Eik-Nes, James C Huhta, Stephen L Luther. J Matern Fetal Neonatal Med 2006
93
5

Prenatal diagnosis of congenital disorder of glycosylation type Ia (CDG-Ia) by cordocentesis and transferrin isoelectric focussing of serum of a 27-week fetus with non-immune hydrops.
Matthew Edwards, Fiona McKenzie, Stephen O'callaghan, David Somerset, Phillip Woodford, Jillian Spilsbury, Michael Fietz, Janice Fletcher. Prenat Diagn 2006
31
12

Transaldolase deficiency: a new cause of hydrops fetalis and neonatal multi-organ disease.
Vassili Valayannopoulos, Nanda M Verhoeven, Karine Mention, Gajja S Salomons, Danièle Sommelet, Marie Gonzales, Guy Touati, Pascale de Lonlay, Cornelis Jakobs, Jean-Marie Saudubray. J Pediatr 2006
57
7


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.