A citation-based method for searching scientific literature

Diana W Bianchi. Am J Med Genet C Semin Med Genet 2019
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting.
Claus H Gravholt, Niels H Andersen, Gerard S Conway, Olaf M Dekkers, Mitchell E Geffner, Karen O Klein, Angela E Lin, Nelly Mauras, Charmian A Quigley, Karen Rubin,[...]. Eur J Endocrinol 2017
388
37

Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome.
Kirstine Stochholm, Svend Juul, Knud Juel, Rune Weis Naeraa, Claus Højbjerg Gravholt. J Clin Endocrinol Metab 2006
365
31

The genetic basis of Turner syndrome aortopathy.
Holly Corbitt, Jacob Gutierrez, Michael Silberbach, Cheryl L Maslen. Am J Med Genet C Semin Med Genet 2019
9
33

TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome.
Holly Corbitt, Shaine A Morris, Claus H Gravholt, Kristian H Mortensen, Rebecca Tippner-Hedges, Michael Silberbach, Cheryl L Maslen. PLoS Genet 2018
31
18

Cardiovascular imaging in Turner syndrome: state-of-the-art practice across the lifespan.
Kristian H Mortensen, Luciana Young, Julie De Backer, Michael Silberbach, Ronnie Thomas Collins, Anthonie L Duijnhouwer, Bejal Pandya, Claus H Gravholt, Leo Lopez, Jolien W Roos-Hesselink. Heart 2018
15
20

Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study.
Agnethe Berglund, Mette Hansen Viuff, Anne Skakkebæk, Simon Chang, Kirstine Stochholm, Claus Højbjerg Gravholt. Orphanet J Rare Dis 2019
32
18

Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry.
Siddharth K Prakash, Carolyn A Bondy, Cheryl L Maslen, Michael Silberbach, Angela E Lin, Laura Perrone, Giuseppe Limongelli, Hector I Michelena, Eduardo Bossone, Rodolfo Citro,[...]. Am J Med Genet A 2016
31
18

Presence of fetal DNA in maternal plasma and serum.
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
18

Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet Med 2016
332
18

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
Karuna R M van der Meij, Erik A Sistermans, Merryn V E Macville, Servi J C Stevens, Caroline J Bax, Mireille N Bekker, Caterina M Bilardo, Elles M J Boon, Marjan Boter, Karin E M Diderich,[...]. Am J Hum Genet 2019
81
18

Social skills and relationships in Turner syndrome.
Jeanne Wolstencroft, David Skuse. Curr Opin Psychiatry 2019
12
16

The deep biology of cognition: Moving toward a comprehensive neurodevelopmental model of Turner syndrome.
Rebecca C Knickmeyer, Stephen R Hooper. Am J Med Genet C Semin Med Genet 2019
7
28

How do genes that escape from X-chromosome inactivation contribute to Turner syndrome?
Samantha B Peeters, Andrea J Korecki, Sarah E L Baldry, Christine Yang, Kira Tosefsky, Bradley P Balaton, Elizabeth M Simpson, Carolyn J Brown. Am J Med Genet C Semin Med Genet 2019
5
40



The Turner syndrome research registry: Creating equipoise between investigators and participants.
Siddharth K Prakash, Soniely Lugo-Ruiz, Michelle Rivera-Dávila, Nunilo Rubio, Avni N Shah, Rebecca C Knickmeyer, Cindy Scurlock, Melissa Crenshaw, Shanlee M Davis, Gary A Lorigan,[...]. Am J Med Genet C Semin Med Genet 2019
6
33

Cardiometabolic health in Turner syndrome.
Shanlee M Davis, Mitchell E Geffner. Am J Med Genet C Semin Med Genet 2019
9
22

Epigenetics and genomics in Turner syndrome.
Mette Viuff, Anne Skakkebaek, Morten M Nielsen, Simon Chang, Claus H Gravholt. Am J Med Genet C Semin Med Genet 2019
12
16

Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome.
Frank J Probst, Mitchell Lance Cooper, Sau Wai Cheung, Monica J Justice. J Hered 2008
22
12

The mouse as a model of fundamental concepts related to Turner syndrome.
Arthur P Arnold. Am J Med Genet C Semin Med Genet 2019
6
33

X-chromosome gene dosage and the risk of diabetes in Turner syndrome.
Vladimir K Bakalov, Clara Cheng, Jian Zhou, Carolyn A Bondy. J Clin Endocrinol Metab 2009
65
12

Coronary artery anomalies in Turner Syndrome.
Mette H Viuff, Christian Trolle, Jan Wen, Jesper M Jensen, Bjarne L Nørgaard, Ephraim J Gutmark, Iris Gutmark-Little, Kristian H Mortensen, Claus Højbjerg Gravholt, Niels H Andersen. J Cardiovasc Comput Tomogr 2016
21
12

A population-based analysis of mortality in patients with Turner syndrome and hypoplastic left heart syndrome using the Texas Birth Defects Registry.
Diego A Lara, Mary K Ethen, Mark A Canfield, Wendy N Nembhard, Shaine A Morris. Congenit Heart Dis 2017
19
12


Widespread DNA hypomethylation and differential gene expression in Turner syndrome.
Christian Trolle, Morten Muhlig Nielsen, Anne Skakkebæk, Philippe Lamy, Søren Vang, Jakob Hedegaard, Iver Nordentoft, Torben Falck Ørntoft, Jakob Skou Pedersen, Claus Højbjerg Gravholt. Sci Rep 2016
59
12

Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome.
Mette Hansen Viuff, Kirstine Stochholm, Niels Uldbjerg, Birgitte Bruun Nielsen, Claus Højbjerg Gravholt. Hum Reprod 2015
30
12

Mortality in women with turner syndrome in Great Britain: a national cohort study.
Minouk J Schoemaker, Anthony J Swerdlow, Craig D Higgins, Alan F Wright, Patricia A Jacobs. J Clin Endocrinol Metab 2008
171
12

Lipid abnormalities in Turner syndrome.
J L Ross, P Feuillan, L M Long, K Kowal, H Kushner, G B Cutler. J Pediatr 1995
72
12

Cardiovascular phenotype in Turner syndrome--integrating cardiology, genetics, and endocrinology.
Kristian H Mortensen, Niels H Andersen, Claus H Gravholt. Endocr Rev 2012
117
12

Heart Transplantation in Children with Turner Syndrome: Analysis of a Linked Dataset.
Joshua D Chew, Jonathan H Soslow, Cary Thurm, Matt Hall, Debra A Dodd, Brian Feingold, Jill Simmons, Justin Godown. Pediatr Cardiol 2018
5
40

The Turner syndrome life course project: Karyotype-phenotype analyses across the lifespan.
Antoinette Cameron-Pimblett, Clementina La Rosa, Thomas F J King, Melanie C Davies, Gerard S Conway. Clin Endocrinol (Oxf) 2017
55
12

Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis.
Sian Taylor-Phillips, Karoline Freeman, Julia Geppert, Adeola Agbebiyi, Olalekan A Uthman, Jason Madan, Angus Clarke, Siobhan Quenby, Aileen Clarke. BMJ Open 2016
168
12

Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks' gestation: relation to maternal and fetal characteristics.
G Ashoor, A Syngelaki, L C Y Poon, J C Rezende, K H Nicolaides. Ultrasound Obstet Gynecol 2013
214
12

Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis.
M M Gil, V Accurti, B Santacruz, M N Plana, K H Nicolaides. Ultrasound Obstet Gynecol 2017
276
12

DEGUM, ÖGUM, SGUM and FMF Germany Recommendations for the Implementation of First-Trimester Screening, Detailed Ultrasound, Cell-Free DNA Screening and Diagnostic Procedures.
Peter Kozlowski, Tilo Burkhardt, Ulrich Gembruch, Markus Gonser, Christiane Kähler, Karl-Oliver Kagan, Constantin von Kaisenberg, Philipp Klaritsch, Eberhard Merz, Horst Steiner,[...]. Ultraschall Med 2019
16
12

Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments.
Kun Sun, Peiyong Jiang, K C Allen Chan, John Wong, Yvonne K Y Cheng, Raymond H S Liang, Wai-kong Chan, Edmond S K Ma, Stephen L Chan, Suk Hang Cheng,[...]. Proc Natl Acad Sci U S A 2015
334
12


Diagnosis of fetal non-chromosomal abnormalities on routine ultrasound examination at 11-13 weeks' gestation.
A Syngelaki, A Hammami, S Bower, V Zidere, R Akolekar, K H Nicolaides. Ultrasound Obstet Gynecol 2019
69
12

Cell-free DNA testing of an extended range of chromosomal anomalies: clinical experience with 6,388 consecutive cases.
Graziano Pescia, Nicolas Guex, Christian Iseli, Liam Brennan, Magne Osteras, Ioannis Xenarios, Laurent Farinelli, Bernard Conrad. Genet Med 2017
50
12


Turner syndrome and associated problems in Turkish children: a multicenter study.
Ediz Yeşilkaya, Abdullah Bereket, Feyza Darendeliler, Firdevs Baş, Şükran Poyrazoğlu, Banu Küçükemre Aydın, Şükran Darcan, Bumin Dündar, Muammer Büyükinan, Cengiz Kara,[...]. J Clin Res Pediatr Endocrinol 2015
28
12

Turner syndrome: mechanisms and management.
Claus H Gravholt, Mette H Viuff, Sara Brun, Kirstine Stochholm, Niels H Andersen. Nat Rev Endocrinol 2019
57
12

The state of Turner syndrome science: Are we on the threshold of discovery?
Paul Kruszka, Michael Silberbach. Am J Med Genet C Semin Med Genet 2019
5
40

Whole-Exome Sequencing for Diagnosis of Turner Syndrome: Toward Next-Generation Sequencing and Newborn Screening.
David R Murdock, Frank X Donovan, Settara C Chandrasekharappa, Nicole Banks, Carolyn Bondy, Maximilian Muenke, Paul Kruszka. J Clin Endocrinol Metab 2017
16
12

Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior years.
Angela E Lin, Siddharth K Prakash, Niels H Andersen, Mette H Viuff, Lynne L Levitsky, Michelle Rivera-Davila, Melissa L Crenshaw, Lars Hansen, Mary K Colvin, Frances J Hayes,[...]. Am J Med Genet A 2019
11
18

DNA sequencing versus standard prenatal aneuploidy screening.
Diana W Bianchi, R Lamar Parker, Jeffrey Wentworth, Rajeevi Madankumar, Craig Saffer, Anita F Das, Joseph A Craig, Darya I Chudova, Patricia L Devers, Keith W Jones,[...]. N Engl J Med 2014
398
12

Cardiovascular Health in Turner Syndrome: A Scientific Statement From the American Heart Association.
Michael Silberbach, Jolien W Roos-Hesselink, Niels H Andersen, Alan C Braverman, Nicole Brown, R Thomas Collins, Julie De Backer, Kim A Eagle, Loren F Hiratzka, Walter H Johnson,[...]. Circ Genom Precis Med 2018
62
12

Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts.
Sung K Kim, Gregory Hannum, Jennifer Geis, John Tynan, Grant Hogg, Chen Zhao, Taylor J Jensen, Amin R Mazloom, Paul Oeth, Mathias Ehrich,[...]. Prenat Diagn 2015
116
12

Low fetal fraction of cell-free DNA predicts placental dysfunction and hypertensive disease in pregnancy.
Kristin D Gerson, Samantha Truong, Miriam J Haviland, Barbara M O'Brien, Michele R Hacker, Melissa H Spiel. Pregnancy Hypertens 2019
20
12

Clinical experience with sex chromosome aneuploidies detected by noninvasive prenatal testing (NIPT): Accuracy and patient decision-making.
Aarti Ramdaney, Jennifer Hoskovec, Jacqueline Harkenrider, Eleazar Soto, Lauren Murphy. Prenat Diagn 2018
25
12


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.