A citation-based method for searching scientific literature

Sarah T South, Charles Lee, Allen N Lamb, Anne W Higgins, Hutton M Kearney. Genet Med 2013
Times Cited: 161



Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
Times Cited: 513




List of shared articles



Times cited

Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with congenital cystic adenomatoid malformation by chromosomal microarray analysis.
Qiong Deng, Lihua Huang, Juan Liu, Fu Fang, Zequn Liu, Yongling Zhang, Fatao Li, Can Liao. J Matern Fetal Neonatal Med 2021
1

Risk of Clinically Significant Chromosomal Microarray Analysis Findings in Fetuses With Nuchal Translucency From 3.0 mm Through 3.4 mm.
Lena Sagi-Dain, Amihood Singer, Shay Ben Shachar, Sagi Josefsberg Ben Yehoshua, Michal Feingold-Zadok, Lior Greenbaum, Idit Maya. Obstet Gynecol 2021
1

Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.
Farah Qaiser, Yue Yin, Carolyn B Mervis, Colleen A Morris, Bonita P Klein-Tasman, Elaine Tam, Lucy R Osborne, Ryan K C Yuen. Orphanet J Rare Dis 2021
1

Clinical Application of Easychip 8x15K Platform in 4106 Pregnancies Without Ultrasound Anomalies.
Valeria Orlando, Viola Alesi, Gianluca Di Giacomo, Michela Canestrelli, Chiara Calacci, Anna Maria Nardone, Giusy Calvieri, Maria Teresa Liambo, Ester Sallicandro, Silvia Di Tommaso,[...]. Reprod Sci 2021
0

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, Atlas Khan, Sarah E Graham, Maddalena Marasà, Hyunwoo Kim, Tze Y Lim, Patricia L Weng, Elena Sánchez-Rodríguez,[...]. J Am Soc Nephrol 2021
0


New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.
Majed J Dasouki, Salma M Wakil, Olfat Al-Harazi, Maarab Alkorashy, Nzioka P Muiya, Editha Andres, Samya Hagos, Haya Aldusery, Nduna Dzimiri, Dilek Colak. OMICS 2020
1

Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defects.
Stela Z Berisha, Shashi Shetty, Thomas W Prior, Anna L Mitchell. Birth Defects Res 2020
1

46,XX Testicular Disorders of Sex Development With DMD Gene Mutation: First Case Report Identified Prenatally by Integrated Analyses in China.
Jianlian Deng, Haoqing Zhang, Caiyun Li, Hui Huang, Saijun Liu, Huanming Yang, Kaili Xie, Qiong Wang, Dongzhu Lei, Jing Wu. Front Genet 2020
2

Nonimmune hydrops fetalis: Genetic analysis and clinical outcome.
Qiong Deng, Fang Fu, Qiuxia Yu, Ru Li, Fucheng Li, Dan Wang, Tingying Lei, Xin Yang, Can Liao. Prenat Diagn 2020
1

Detection of chromosomal abnormalities in spontaneous miscarriage by low‑coverage next‑generation sequencing.
Fen-Xia Li, Mei-Juan Xie, Shou-Fang Qu, Dan He, Long Wu, Zhi-Kun Liang, Ying-Song Wu, Fang Yang, Xue-Xi Yang. Mol Med Rep 2020
1

Limited diagnostic impact of duplications <1 Mb of uncertain clinical significance: a 10-year retrospective analysis of reporting practices at the Mayo Clinic.
Cherisse A Marcou, Beth Pitel, Clinton E Hagen, Nicole J Boczek, Ross A Rowsey, Linda B Baughn, Nicole L Hoppman, Erik C Thorland, Hutton M Kearney. Genet Med 2020
0

Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations.
Chenyang Xu, Yanbao Xiang, Xueqin Xu, Lili Zhou, Huanzheng Li, Xueqin Dong, Shaohua Tang. Mol Cytogenet 2020
1


European guidelines for constitutional cytogenomic analysis.
Marisa Silva, Nicole de Leeuw, Kathy Mann, Heleen Schuring-Blom, Sian Morgan, Daniela Giardino, Katrina Rack, Ros Hastings. Eur J Hum Genet 2019
31

Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease.
Andrew M Gross, Subramanian S Ajay, Vani Rajan, Carolyn Brown, Krista Bluske, Nicole J Burns, Aditi Chawla, Alison J Coffey, Alka Malhotra, Alicia Scocchia,[...]. Genet Med 2019
32

MLPA is a practical and complementary alternative to CMA for diagnostic testing in patients with autism spectrum disorders and identifying new candidate CNVs associated with autism.
Pavlina Capkova, Josef Srovnal, Zuzana Capkova, Katerina Staffova, Vera Becvarova, Marie Trkova, Katerina Adamova, Alena Santava, Vaclava Curtisova, Marian Hajduch,[...]. PeerJ 2019
2


A novel case of global developmental delay syndrome with microdeletion at 10p14-p15.3 and microduplication at 18p11.31-p11.32.
Danyan Zhang, Yijian Zhu, Xuefei Feng, Limeng Dai, Mingfu Ma, Lianbing Li, Hong Guo, Letian Zhao, Yuping Zhang, Yun Bai. Medicine (Baltimore) 2019
0

Possibility of early diagnosis in a fetus affected by Prader‑Willi syndrome with maternal hetero‑UPD15: A lesson to be learned.
Yanling Dong, Shu Liu, Junnan Li, Jian Li, Qian Chen, Jianyun Luo, Chunlei Li, Huifan Li, Hongbo Qi, Rong Li. Mol Med Rep 2019
4

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.
Matthew Hoi Kin Chau, Ye Cao, Yvonne Ka Yin Kwok, Samantha Chan, Yiu Man Chan, Huilin Wang, Zhenjun Yang, Hoi Kin Wong, Tak Yeung Leung, Kwong Wai Choy. Am J Obstet Gynecol 2019
12

Subchromosomal anomalies in small for gestational-age fetuses and newborns.
Ying Ma, Yan Pei, Chenghong Yin, Yuxin Jiang, Jingjing Wang, Xiaofei Li, Lin Li, Karl Oliver Kagan, Qingqing Wu. Arch Gynecol Obstet 2019
2


Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.
Zirui Dong, Junhao Yan, Fengping Xu, Jianying Yuan, Hui Jiang, Huilin Wang, Haixiao Chen, Lei Zhang, Lingfei Ye, Jinjin Xu,[...]. Am J Hum Genet 2019
15

Microarray findings in pregnancies with oligohydramnios - a retrospective cohort study and literature review.
Amihood Singer, Idit Maya, Rivka Sukenik-Halevy, Tamar Tenne, Dorit Lev, Shay Ben Shachar, Lena Sagi-Dain. J Perinat Med 2019
2

A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings.
Hongyan Chai, Autumn DiAdamo, Brittany Grommisch, Fang Xu, Qinghua Zhou, Jiadi Wen, Maurice Mahoney, Allen Bale, James McGrath, Michele Spencer-Manzon,[...]. Front Genet 2019
4


Genomic medicine for kidney disease.
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
46

Microarray analysis in pregnancies with isolated unilateral kidney agenesis.
Lena Sagi-Dain, Idit Maya, Amir Peleg, Adi Reches, Ehud Banne, Hagit N Baris, Tamar Tenne, Amihood Singer, Shay Ben-Shachar. Pediatr Res 2018
6

The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis.
Melissa Stosic, Brynn Levy, Ronald Wapner. Obstet Gynecol Clin North Am 2018
18