A citation-based method for searching scientific literature

Min Zhang, Hailong Huang, Na Lin, Shuqiong He, Gang An, Yan Wang, Meihuan Chen, Lingji Chen, Yuan Lin, Liangpu Xu. J Clin Lab Anal 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


X-linked ichthyosis: Clinical and molecular findings in 35 Italian patients.
Andrea Diociaiuti, Adriano Angioni, Elisa Pisaneschi, Viola Alesi, Giovanna Zambruno, Antonio Novelli, May El Hachem. Exp Dermatol 2019
10
100

X-linked ichthyosis associated with psychosis and behavioral abnormalities: a case report.
Amna Malik, Ahmed Bait Amer, Mohammed Salama, Bander Haddad, Muhammad T Alrifai, Mohammed Al Balwi, William Davies, Wafaa Eyaid. J Med Case Rep 2017
11
66

X-linked ichthyosis: differential diagnosis of low maternal oestriol level.
O Liaugaudienė, E Benušienė, I Domarkienė, L Ambrozaitytė, V Kučinskas. J Obstet Gynaecol 2014
1
100

In vivo confocal microscopy of pre-Descemet corneal dystrophy associated with X-linked ichthyosis: a case report.
Hui Shi, Xiao-Feng Qi, Tao-Tao Liu, Qian Hao, Xiao-Hong Li, Ling-Ling Liang, Yi-Miao Wang, Zhi-Hua Cui. BMC Ophthalmol 2017
4
33



Inherited ichthyosis: Non-syndromic forms.
Takuya Takeichi, Masashi Akiyama. J Dermatol 2016
76
33


Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols.
Sylvie Langlois, Linlea Armstrong, Kim Gall, Gurdip Hulait, Janet Livingston, Tanya Nelson, Patricia Power, Denise Pugash, Dawn Siciliano, Michelle Steinraths,[...]. Prenat Diagn 2009
14
33

A Case of Syndromic X-linked Ichthyosis with Léri-Weill Dyschondrosteosis.
Claire Abasq-Thomas, Sébastien Schmitt, Emilie Brenaut, Chantal Metz, Jean Chiesa, Laurent Misery. Acta Derm Venereol 2016
4
33



Prevalence of steroid sulfatase deficiency in California according to race and ethnicity.
Wendy Y Craig, Marie Roberson, Glenn E Palomaki, Cedric H L Shackleton, Josep Marcos, James E Haddow. Prenat Diagn 2010
17
33

X-linked icthyosis. A sulphatase deficiency.
G Koppe, A Marinković-Ilsen, Y Rijken, W P De Groot, A C Jöbsis. Arch Dis Child 1978
62
33


The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray.
Jennifer L Hand, Cassandra K Runke, Jennelle C Hodge. J Am Acad Dermatol 2015
19
33


[Identification of gene mutation and prenatal diagnosis in a family with X-linked ichthyosis].
Ji-Wei Huang, Ning Tang, Wu-Gao Li, Zhe-Tao Li, Shi-Qiang Luo, Jing-Wen Li, Jun Huang, Ti-Zhen Yan. Zhongguo Dang Dai Er Ke Za Zhi 2016
2
50

Banding pattern on polarized hair microscopic examination and unilateral polymicrogyria in a patient with steroid sulfatase deficiency.
Puja K Puri, Deepti M Reddi, Michele Spencer-Manzon, Kristen Deak, Sonya U Steele, Mohamad A Mikati. Arch Dermatol 2012
3
33


Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series.
B Rodrigo-Nicolás, E Bueno-Martínez, A Martín-Santiago, J Cañueto, A Vicente, A Torrelo, L Noguera-Morel, A Duat-Rodríguez, C Jorge-Finnigan, I Palacios-Álvarez,[...]. Br J Dermatol 2018
13
33


X-linked ichthyosis: an oculocutaneous genodermatosis.
Neil F Fernandes, Camila K Janniger, Robert A Schwartz. J Am Acad Dermatol 2010
40
33

Role of cholesterol sulfate in epidermal structure and function: lessons from X-linked ichthyosis.
Peter M Elias, Mary L Williams, Eung-Ho Choi, Kenneth R Feingold. Biochim Biophys Acta 2014
58
33

X-linked recessive ichthyosis.
Carole Hazan, Seth J Orlow, Julie V Schaffer. Dermatol Online J 2005
5
33

Genetic analysis of a 12-year-old boy with X-linked ichthyosis in association with sclerosing glomerulonephritis.
Yijin Song, Jing Chen, Zhuwen Yi, Xiqiang Dang, Dehua Cheng, Xiaochuan Wu, Yueqiu Tan. Mol Med Rep 2013
2
50


Nonsyndromic types of ichthyoses - an update.
Heiko Traupe, Judith Fischer, Vinzenz Oji. J Dtsch Dermatol Ges 2014
51
33

Steroid sulfatase: molecular biology, regulation, and inhibition.
M J Reed, A Purohit, L W L Woo, S P Newman, B V L Potter. Endocr Rev 2005
349
33

Localization of cholesteryl sulfate in human spermatozoa in support of a hypothesis for the mechanism of capacitation.
J Langlais, M Zollinger, L Plante, A Chapdelaine, G Bleau, K D Roberts. Proc Natl Acad Sci U S A 1981
142
33

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
643
33

Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age.
Xiaoqing Wu, Gang An, Xiaorui Xie, Linjuan Su, Meiying Cai, Xuemei Chen, Ying Li, Na Lin, Deqin He, Meiying Wang,[...]. J Clin Lab Anal 2020
6
33


Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
Pauline Chaste, Stephan J Sanders, Kommu N Mohan, Lambertus Klei, Youeun Song, Michael T Murtha, Vanessa Hus, Jennifer K Lowe, A Jeremy Willsey, Daniel Moreno-De-Luca,[...]. Autism Res 2014
44
33

High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power.
Beatrice Oneda, Rosa Baldinger, Regina Reissmann, Irina Reshetnikova, Pavel Krejci, Rahim Masood, Nicole Ochsenbein-Kölble, Deborah Bartholdi, Katharina Steindl, Denise Morotti,[...]. Prenat Diagn 2014
29
33

Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result.
Laia Rodriguez-Revenga, Irene Madrigal, Antoni Borrell, Josep M Martinez, Joan Sabria, Lourdes Martin, Wladimiro Jimenez, Aurea Mira, Celia Badenas, Montserrat Milà. Clin Genet 2020
2
50

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.
Idit Maya, Reuven Sharony, Shiri Yacobson, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, Ifaat Agmon-Fishman, Lital Cohen-Vig, Yael Goldberg, Racheli Berger,[...]. Genet Med 2018
27
33

Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis.
Hagit Hochner, Hagit Daum, Liza Douiev, Naama Zvi, Ayala Frumkin, Michal Macarov, Adva Kimchi-Shaal, Nuphar Hacohen, Avital Eilat, Duha Faham,[...]. Obstet Gynecol 2020
6
33


Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study.
Jane L Halliday, Cecile Muller, Taryn Charles, Fiona Norris, Joanne Kennedy, Sharon Lewis, Bettina Meiser, Susan Donath, Zornitza Stark, George McGillivray,[...]. Eur J Hum Genet 2018
11
33

Uptake of noninvasive prenatal testing at a large academic referral center.
Sebastian Larion, Steven L Warsof, Letty Romary, Margaret Mlynarczyk, David Peleg, Alfred Z Abuhamad. Am J Obstet Gynecol 2014
61
33

Role of late amniocentesis in the era of modern genomic technologies.
H Daum, A Ben David, M Nadjari, S Zenvirt, S Helman, N Yanai, V Meiner, S Yagel, A Frumkin, S Shkedi Rafid. Ultrasound Obstet Gynecol 2019
7
33


15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.
Clémence Vanlerberghe, Florence Petit, Valérie Malan, Catherine Vincent-Delorme, Sonia Bouquillon, Odile Boute, Muriel Holder-Espinasse, Bruno Delobel, Bénédicte Duban, Louis Vallee,[...]. Eur J Med Genet 2015
49
33

First and second trimester antenatal screening for Down's syndrome: the results of the Serum, Urine and Ultrasound Screening Study (SURUSS).
N J Wald, C Rodeck, A K Hackshaw, J Walters, L Chitty, A M Mackinson. Health Technol Assess 2003
170
33


Fetal soft markers in obstetric ultrasound.
Michiel C Van den Hof, R Douglas Wilson. J Obstet Gynaecol Can 2005
69
33

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai,[...]. Ultrasound Obstet Gynecol 2021
8
33

Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing.
Xiaoqing Wu, Ying Li, Na Lin, Xiaorui Xie, Linjuan Su, Meiying Cai, Yuan Lin, Linshuo Wang, Meiying Wang, Liangpu Xu,[...]. J Cell Mol Med 2021
1
100

Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.
S L van der Steen, K E M Diderich, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, D Van Opstal, M I Srebniak, A Tibben,[...]. Clin Genet 2015
32
33


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.