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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Attention deficit hyperactivity disorder (ADHD) in phenotypically similar neurogenetic conditions: Turner syndrome and the RASopathies
Tamar Green, Paige E. Naylor, William Davies
Journal of Neurodevelopmental Disorders (2017) Vol. 9, Iss. 1
Open Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

ADHD: Current Concepts and Treatments in Children and Adolescents
Renate Drechsler, Silvia Brem, Daniel Brandeis, et al.
Neuropediatrics (2020) Vol. 51, Iss. 05, pp. 315-335
Open Access | Times Cited: 244
Clinical practice guidelines for the care of girls and women with Turner syndrome
Claus Højbjerg Gravholt, N.H. Andersen, Sophie Christin‐Maître, et al.
European Journal of Endocrinology (2024) Vol. 190, Iss. 6, pp. G53-G151
Open Access | Times Cited: 49
Sex differences in psychiatric disorders: what we can learn from sex chromosome aneuploidies
Tamar Green, Shira Flash, Allan L. Reiss
Neuropsychopharmacology (2018) Vol. 44, Iss. 1, pp. 9-21
Open Access | Times Cited: 152
Turner Syndrome and Psychosocial Interventions: Recommendations for Collaborative Communication Between Medical and School Teams
Mackenzie Z. Norman, Christa Hutaff‐Lee, Rebecca Knickmeyer, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2025)
Closed Access | Times Cited: 1
Neuropsychiatric phenotypes in children with Noonan syndrome
Paige E. Naylor, Jennifer L. Bruno, Sharon Bade Shrestha, et al.
Developmental Medicine & Child Neurology (2023) Vol. 65, Iss. 11, pp. 1520-1529
Closed Access | Times Cited: 19
Loss of Capicua alters early T cell development and predisposes mice to T cell lymphoblastic leukemia/lymphoma
Qiumin Tan, Lorenzo Brunetti, Maxime W.C. Rousseaux, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 7
Open Access | Times Cited: 41
The sixth international RASopathies symposium: Precision medicine—From promise to practice
Karen W. Gripp, Lisa Schill, Lisa Schoyer, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 3, pp. 597-606
Open Access | Times Cited: 38
A familial modeling framework for advancing precision medicine for children with neuropsychiatric disorders
Jennifer L. Bruno, Jacob Joseph Merrin, S. M. Hadi Hosseini, et al.
Developmental Medicine & Child Neurology (2025)
Closed Access
Social skills in children with RASopathies: a comparison of Noonan syndrome and neurofibromatosis type 1
Elizabeth I. Pierpont, Rebekah L. Hudock, Allison M. H. Foy, et al.
Journal of Neurodevelopmental Disorders (2018) Vol. 10, Iss. 1
Open Access | Times Cited: 36
Transcriptomic Dysregulation in Animal Models of Attention‐Deficit Hyperactivity Disorder and Nicotine Dependence Suggests Shared Neural Mechanisms
Sarah Van Horn, Heather Driscoll, Donna J. Toufexis
Brain and Behavior (2025) Vol. 15, Iss. 3
Open Access
Hyperactive MEK1 Signaling in Cortical GABAergic Neurons Promotes Embryonic Parvalbumin Neuron Loss and Defects in Behavioral Inhibition
Michael Holter, Lauren T. Hewitt, Kenji Nishimura, et al.
Cerebral Cortex (2020) Vol. 31, Iss. 6, pp. 3064-3081
Open Access | Times Cited: 18
MANAGEMENT OF ENDOCRINE DISEASE: Transition of care for young adult patients with Turner syndrome
Valérie Bernard, Bruno Donadille, T. Le Poulennec, et al.
European Journal of Endocrinology (2018) Vol. 180, Iss. 1, pp. R1-R7
Open Access | Times Cited: 17
Emotional functioning among children with neurofibromatosis type 1 or Noonan syndrome
Alana M. McNeill, Rebekah L. Hudock, Allison M. H. Foy, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 12, pp. 2433-2446
Closed Access | Times Cited: 17
Social behavior in RASopathies and idiopathic autism
Allison M. H. Foy, Rebekah L. Hudock, Ryan Shanley, et al.
Journal of Neurodevelopmental Disorders (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 9
Altered canonical and striatal-frontal resting state functional connectivity in children with pathogenic variants in the Ras/mitogen-activated protein kinase pathway
Jennifer L. Bruno, Sharon Bade Shrestha, Allan L. Reiss, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 3, pp. 1542-1551
Open Access | Times Cited: 9
Syndrome-Specific Neuroanatomical Phenotypes in Girls With Turner and Noonan Syndromes
Monica Siqueiros Sanchez, Bhavana Rai, Samir Chowdhury, et al.
Biological Psychiatry Cognitive Neuroscience and Neuroimaging (2022) Vol. 9, Iss. 2, pp. 146-155
Open Access | Times Cited: 9
Prenatal Diagnosis of Sex Chromosome Abnormalities
Jeff M. Milunsky
(2009), pp. 273-312
Closed Access | Times Cited: 10
The contribution of Xp22.31 gene dosage to Turner and Klinefelter syndromes and sex-biased phenotypes
William Davies
European Journal of Medical Genetics (2021) Vol. 64, Iss. 4, pp. 104169-104169
Open Access | Times Cited: 8
Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndrome
Federica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 510-519
Open Access | Times Cited: 5
Gender-Specific Fine Motor Skill Learning Is Impaired by Myelin-Targeted Neurofibromatosis Type 1 Gene Mutation
Daniella P. Hernandez, Daniela Maione Nunes Cruz, Celeste S. Martinez, et al.
Cancers (2024) Vol. 16, Iss. 3, pp. 477-477
Open Access
Autism and Social Behavior in RASopathies
Allison M. H. Foy, Rebekah L. Hudock, Elizabeth I. Pierpont
(2024), pp. 611-634
Closed Access
Brain volumes in genetic syndromes associated with mTOR dysregulation: a systematic review and meta-analysis
Jonathan M. Payne, Kristina M. Haebich, Rebecca A Mitchell, et al.
Molecular Psychiatry (2024)
Closed Access
Turner Syndrome
W. Philip Bartel, Robert Accordino, Bushra Awidi, et al.
(2024), pp. 171-189
Closed Access
Epilepsy in cardiofaciocutaneous syndrome: Clinical burden and response to anti‐seizure medication
Daniel Kenney‐Jung, Josue E. Collazo‐Lopez, Dante J. Rogers, et al.
American Journal of Medical Genetics Part A (2023) Vol. 194, Iss. 2, pp. 301-310
Open Access | Times Cited: 1
Turner Syndrome and Attention-Deficit with Hyperactivity Disorder in a Pediatric Population
Tânia B Cavaco, Marta Novo, Sara Soares, et al.
Gazeta Médica (2024), pp. 86-87
Open Access
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