A citation-based method for searching scientific literature

Hayley S Mountford, Dorothy V M Bishop, Paul A Thompson, Nuala H Simpson, Dianne F Newbury. Am J Med Genet C Semin Med Genet 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child.
Kirsten A Riggan, Sharron Close, Megan A Allyse. Am J Med Genet C Semin Med Genet 2020
4
50

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
313
50

Rare sex chromosome variation 48,XXYY: An integrative review.
Amy A Blumling, Kristy Martyn, Amy Talboy, Sharron Close. Am J Med Genet C Semin Med Genet 2020
2
50

The behavioral profile of children aged 1-5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY).
Evelien Urbanus, Hanna Swaab, Nicole Tartaglia, Lisa Cordeiro, Sophie van Rijn. Am J Med Genet C Semin Med Genet 2020
5
50

The current landscape of European registries for rare endocrine conditions.
S R Ali, J Bryce, M Cools, M Korbonits, J G Beun, D Taruscio, T Danne, M Dattani, O M Dekkers, A Linglart,[...]. Eur J Endocrinol 2019
11
50

Addressing gaps in care of people with conditions affecting sex development and maturation.
Olaf Hiort, Martine Cools, Alexander Springer, Ken McElreavey, Andy Greenfield, Stefan A Wudy, Alexandra Kulle, S Faisal Ahmed, Arianne Dessens, Antonio Balsamo,[...]. Nat Rev Endocrinol 2019
13
50

Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis.
Kristen Wigby, Lisa Cordeiro, Rebecca Wilson, Kathleen Angkustsiri, Tony J Simon, Nicole Tartaglia. Am J Med Genet C Semin Med Genet 2020
1
100

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
26
50

Population screening for genetic disorders in the 21st century: evidence, economics, and ethics.
S D Grosse, W H Rogowski, L F Ross, M C Cornel, W J Dondorp, M J Khoury. Public Health Genomics 2010
83
50

A general theory of sexual differentiation.
Arthur P Arnold. J Neurosci Res 2017
102
50

Minipuberty in Klinefelter syndrome: Current status and future directions.
Lise Aksglaede, Shanlee M Davis, Judith L Ross, Anders Juul. Am J Med Genet C Semin Med Genet 2020
4
50

Androgen Treatment Effects on Motor Function, Cognition, and Behavior in Boys with Klinefelter Syndrome.
Judith L Ross, Harvey Kushner, Karen Kowal, Martha Bardsley, Shanlee Davis, Allan L Reiss, Nicole Tartaglia, David Roeltgen. J Pediatr 2017
34
50

Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention.
Nicole Tartaglia, Susan Howell, Shanlee Davis, Karen Kowal, Tanea Tanda, Mariah Brown, Cristina Boada, Amanda Alston, Leah Crawford, Talia Thompson,[...]. Am J Med Genet C Semin Med Genet 2020
4
50

Executive function in XXY: Comparison of performance-based measures and rating scales.
Jennifer Janusz, Caroline Harrison, Cristina Boada, Lisa Cordeiro, Susan Howell, Nicole Tartaglia, Richard Boada. Am J Med Genet C Semin Med Genet 2020
2
50

X Inactivation and Escape: Epigenetic and Structural Features.
He Fang, Christine M Disteche, Joel B Berletch. Front Cell Dev Biol 2019
24
50

Sex chromosome aneuploidy alters the relationship between neuroanatomy and cognition.
Allysa Warling, Siyuan Liu, Kathleen Wilson, Ethan Whitman, François M Lalonde, Liv S Clasen, Jonathan D Blumenthal, Armin Raznahan. Am J Med Genet C Semin Med Genet 2020
4
50

Psychological functioning, brain morphology, and functional neuroimaging in Klinefelter syndrome.
Anne Skakkebaek, Claus H Gravholt, Simon Chang, Philip J Moore, Mikkel Wallentin. Am J Med Genet C Semin Med Genet 2020
3
50



Morbidity in Klinefelter syndrome and the effect of testosterone treatment.
Simon Chang, Anne Skakkebaek, Shanlee M Davis, Claus H Gravholt. Am J Med Genet C Semin Med Genet 2020
3
50

Neuropsychological functions, sleep, and mental health in adults with Klinefelter syndrome.
Krister W Fjermestad, Rene Huster, Christina Thunberg, Simen Stokke, Claus H Gravholt, Anne-Kristin Solbakk. Am J Med Genet C Semin Med Genet 2020
2
50

Oxandrolone Treatment Results in an Increased Risk of Gonadarche in Prepubertal Boys With Klinefelter Syndrome.
Shanlee M Davis, Najiba Lahlou, Matthew Cox-Martin, Karen Kowal, Philip S Zeitler, Judith L Ross. J Clin Endocrinol Metab 2018
10
50

Metabolic and cardiovascular risk factors in Klinefelter syndrome.
Matteo Spaziani, Antonio F Radicioni. Am J Med Genet C Semin Med Genet 2020
5
50

Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies.
Talia Thompson, Susan Howell, Shanlee Davis, Rebecca Wilson, Jennifer Janusz, Richard Boada, Laura Pyle, Nicole Tartaglia. Am J Med Genet C Semin Med Genet 2020
4
50

Human sex chromosome aneuploidies: The hypothalamic-pituitary-gonadal axis.
Alan D Rogol. Am J Med Genet C Semin Med Genet 2020
4
50

41,XXY * male mice: An animal model for Klinefelter syndrome.
Joachim Wistuba, Cristin Beumer, Ralph Brehm, Jörg Gromoll. Am J Med Genet C Semin Med Genet 2020
2
50

Genes that escape from X-chromosome inactivation: Potential contributors to Klinefelter syndrome.
Maria Jose Navarro-Cobos, Bradley P Balaton, Carolyn J Brown. Am J Med Genet C Semin Med Genet 2020
6
50

High prevalence of cardiometabolic risk features in adolescents with 47,XXY/Klinefelter syndrome.
Shanlee M Davis, Sophia DeKlotz, Kristen J Nadeau, Megan M Kelsey, Philip S Zeitler, Nicole R Tartaglia. Am J Med Genet C Semin Med Genet 2020
4
50

Testosterone Treatment in Infants With 47,XXY: Effects on Body Composition.
Shanlee M Davis, Regina M Reynolds, Dana M Dabelea, Philip S Zeitler, Nicole R Tartaglia. J Endocr Soc 2019
13
50

The epidemiology of sex chromosome abnormalities.
Agnethe Berglund, Kirstine Stochholm, Claus Højbjerg Gravholt. Am J Med Genet C Semin Med Genet 2020
4
50

Confirmatory testing illustrates additional risks for structural sex chromosome abnormalities in fetuses with a non-invasive prenatal screen positive for monosomy X.
Kristen L Sund, Divya Khattar, Theresa Boomer, Samantha Caldwell, Lisa Dyer, Robert J Hopkin, Teresa A Smolarek. Am J Med Genet C Semin Med Genet 2020
2
50

Specific learning disorders in sex chromosome aneuploidies: Neural circuits of literacy and mathematics.
Iliana I Karipidis, David S Hong. Am J Med Genet C Semin Med Genet 2020
2
50

Germ cell loss in Klinefelter syndrome: When and why?
Margo Willems, Inge Gies, Dorien Van Saen. Am J Med Genet C Semin Med Genet 2020
2
50

Klinefelter syndrome and testosterone treatment: a national cohort study on thrombosis risk.
Simon Chang, Christian Fynbo Christiansen, Anders Bojesen, Svend Juul, Anna-Marie B Münster, Claus H Gravholt. Endocr Connect 2020
12
50

Epigenetic and transcriptomic consequences of excess X-chromosome material in 47,XXX syndrome-A comparison with Turner syndrome and 46,XX females.
Morten Muhlig Nielsen, Christian Trolle, Søren Vang, Henrik Hornshøj, Anne Skakkebaek, Jakob Hedegaard, Iver Nordentoft, Jakob Skou Pedersen, Claus Højbjerg Gravholt. Am J Med Genet C Semin Med Genet 2020
1
100

Testicular function in boys with 47,XYY and relationship to phenotype.
Shanlee M Davis, Luke Bloy, Timothy P L Roberts, Karen Kowal, Amanda Alston, Aysha Tahsin, Alyssa Truxon, Judith L Ross. Am J Med Genet C Semin Med Genet 2020
3
50

Positive effects of early androgen therapy on the behavioral phenotype of boys with 47,XXY.
Carole Samango-Sprouse, Emily J Stapleton, Patrick Lawson, Francie Mitchell, Teresa Sadeghin, Sherida Powell, Andrea L Gropman. Am J Med Genet C Semin Med Genet 2015
53
50

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
28
50

The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy.
Nicole Tartaglia, Susan Howell, Rebecca Wilson, Jennifer Janusz, Richard Boada, Sydney Martin, Jacqueline B Frazier, Michelle Pfeiffer, Karen Regan, Sarah McSwegin,[...]. J Multidiscip Healthc 2015
19
50

Developmental coordination disorder and overweight and obesity in children aged 9-14 y.
J Cairney, J A Hay, B E Faught, R Hawes. Int J Obes (Lond) 2005
124
50

Coordination difficulties, IQ and psychopathology in children with high-risk copy number variants.
Adam C Cunningham, Jeremy Hall, Michael J Owen, Marianne B M van den Bree. Psychol Med 2021
3
50


A comparison of developmental coordination disorder prevalence rates in Canadian and Greek children.
Georgia D Tsiotra, Andreas D Flouris, Yiannis Koutedakis, Brent E Faught, Alan M Nevill, Andrew M Lane, Nicolaos Skenteris. J Adolesc Health 2006
44
50

Improved whole-chromosome phasing for disease and population genetic studies.
Olivier Delaneau, Jean-Francois Zagury, Jonathan Marchini. Nat Methods 2013
740
50

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood.
Paul Lichtenstein, Eva Carlström, Maria Råstam, Christopher Gillberg, Henrik Anckarsäter. Am J Psychiatry 2010
388
50

Determinants of developmental coordination disorder in 7-year-old children: a study of children in the Danish National Birth Cohort.
Rikke Faebo Larsen, Laust Hvas Mortensen, Torben Martinussen, Anne-Marie Nybo Andersen. Dev Med Child Neurol 2013
26
50

International clinical practice recommendations on the definition, diagnosis, assessment, intervention, and psychosocial aspects of developmental coordination disorder.
Rainer Blank, Anna L Barnett, John Cairney, Dido Green, Amanda Kirby, Helene Polatajko, Sara Rosenblum, Bouwien Smits-Engelsman, David Sugden, Peter Wilson,[...]. Dev Med Child Neurol 2019
121
50

The BRAG/IQSec family of Arf GEFs.
Ryan S D'Souza, James E Casanova. Small GTPases 2016
11
50

DCD and ADHD: a genetic study of their shared aetiology.
Neilson C Martin, Jan P Piek, David Hay. Hum Mov Sci 2006
89
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.