A citation-based method for searching scientific literature

Christine M Freitag, Andreas G Chiocchetti, Denise Haslinger, Afsheen Yousaf, Regina Waltes. Z Kinder Jugendpsychiatr Psychother 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology.
Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, Samuel J R A Chawner, Kirsten A Donald, Marianne B M van den Bree, Jonathan Sebat, David H Ledbetter, John N Constantino, Rachel K Earl,[...]. Am J Psychiatry 2022
8
66

Novel treatments in autism spectrum disorder.
Danielle Baribeau, Jacob Vorstman, Evdokia Anagnostou. Curr Opin Psychiatry 2022
5
66

Genetic Findings as the Potential Basis of Personalized Pharmacotherapy in Phelan-McDermid Syndrome.
Brianna Dyar, Erika Meaddough, Sara M Sarasua, Curtis Rogers, Katy Phelan, Luigi Boccuto. Genes (Basel) 2021
7
66

Somatic Mosaicism and Autism Spectrum Disorder.
Alissa M D'Gama. Genes (Basel) 2021
4
66


Translating the Role of mTOR- and RAS-Associated Signalopathies in Autism Spectrum Disorder: Models, Mechanisms and Treatment.
Verica Vasic, Mattson S O Jones, Denise Haslinger, Lisa S Knaus, Michael J Schmeisser, Gaia Novarino, Andreas G Chiocchetti. Genes (Basel) 2021
2
100


Longitudinal Changes in Cortical Thickness in Adolescents with Autism Spectrum Disorder and Their Association with Restricted and Repetitive Behaviors.
Valentina Bieneck, Anke Bletsch, Caroline Mann, Tim Schäfer, Hanna Seelemeyer, Njål Herøy, Jennifer Zimmermann, Charlotte Marie Pretzsch, Elke Hattingen, Christine Ecker. Genes (Basel) 2021
3
66

Gene Therapies for Monogenic Autism Spectrum Disorders.
Wout Weuring, Jeroen Geerligs, Bobby P C Koeleman. Genes (Basel) 2021
6
66

Following Excitation/Inhibition Ratio Homeostasis from Synapse to EEG in Monogenetic Neurodevelopmental Disorders.
Lisa Geertjens, Torben W van Voorst, Arianne Bouman, Maaike A van Boven, Tjitske Kleefstra, Matthijs Verhage, Klaus Linkenkaer-Hansen, Nael Nadif Kasri, L Niels Cornelisse, Hilgo Bruining. Genes (Basel) 2022
2
100

Kurzzeitige Behandlung von Patient_innen mit Anorexia nervosa mit rekombinant hergestelltem Human-Leptin (Metreleptin): Rasch einsetzende positive Effekte auf Stimmung, Kognition und Verhalten.
Johannes Hebebrand, Jochen Antel, Susanne Tan, Martin Wabitsch, Urban Wiesing, Nikolaus Barth, Christine Ludwig, Judith Bühlmeier, Lars Libuda, Gabriella Milos,[...]. Z Kinder Jugendpsychiatr Psychother 2021
3
33

[Genetic Analyses of Complex Phenotypes Through the Example of Anorexia Nervosa and Bodyweight Regulation].
Raphael Hirtz, Yiran Zheng, Luisa S Rajcsanyi, Lars Libuda, Jochen Antel, Triinu Peters, Johannes Hebebrand, Anke Hinney. Z Kinder Jugendpsychiatr Psychother 2021
1
100

[The Gut Microbiome and Its Clinical Implications in Anorexia Nervosa].
Stefanie Trinh, Lara Keller, Jochen Seitz. Z Kinder Jugendpsychiatr Psychother 2021
1
100

[The Genetic Basis of ADHD - An Update].
Sarah Hohmann, Alexander Häge, Sabina Millenet, Tobias Banaschewski. Z Kinder Jugendpsychiatr Psychother 2021
1
100

[Nutrition and mental health - how findings from genetic studies can support the identification of dietary effects].
Lars Libuda, Johannes Hebebrand, Manuel Föcker, Triinu Peters, Anke Hinney. Z Kinder Jugendpsychiatr Psychother 2021
1
100


Recent Advances in Understanding the Genetic Architecture of Autism.
Caroline M Dias, Christopher A Walsh. Annu Rev Genomics Hum Genet 2020
17
33


What we can learn from a genetic rodent model about autism.
Dorit Möhrle, Marta Fernández, Olga Peñagarikano, Andreas Frick, Brian Allman, Susanne Schmid. Neurosci Biobehav Rev 2020
24
33

Project AIM: Autism intervention meta-analysis for studies of young children.
Micheal Sandbank, Kristen Bottema-Beutel, Shannon Crowley, Margaret Cassidy, Kacie Dunham, Jacob I Feldman, Jenna Crank, Susanne A Albarran, Sweeya Raj, Prachy Mahbub,[...]. Psychol Bull 2020
137
33

Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder.
Kristiina Tammimies, Danyang Li, Ielyzaveta Rabkina, Sofia Stamouli, Martin Becker, Veronika Nicolaou, Steve Berggren, Christina Coco, Torbjörn Falkmer, Ulf Jonsson,[...]. Sci Rep 2019
10
33

The Lancet Commission on the future of care and clinical research in autism.
Catherine Lord, Tony Charman, Alexandra Havdahl, Paul Carbone, Evdokia Anagnostou, Brian Boyd, Themba Carr, Petrus J de Vries, Cheryl Dissanayake, Gauri Divan,[...]. Lancet 2022
82
33


The road to precision psychiatry: translating genetics into disease mechanisms.
Michael J Gandal, Virpi Leppa, Hyejung Won, Neelroop N Parikshak, Daniel H Geschwind. Nat Neurosci 2016
125
33

Prevalence of co-occurring mental health diagnoses in the autism population: a systematic review and meta-analysis.
Meng-Chuan Lai, Caroline Kassee, Richard Besney, Sarah Bonato, Laura Hull, William Mandy, Peter Szatmari, Stephanie H Ameis. Lancet Psychiatry 2019
390
33

Systematic review of tools to measure outcomes for young children with autism spectrum disorder.
Helen McConachie, Jeremy R Parr, Magdalena Glod, Jennifer Hanratty, Nuala Livingstone, Inalegwu P Oono, Shannon Robalino, Gillian Baird, Bryony Beresford, Tony Charman,[...]. Health Technol Assess 2015
128
33

A Meta-analysis of Outcome Studies of Autistic Adults: Quantifying Effect Size, Quality, and Meta-regression.
David Mason, Simone J Capp, Gavin R Stewart, Matthew J Kempton, Karen Glaser, Patricia Howlin, Francesca Happé. J Autism Dev Disord 2021
21
33

Heritability of autism spectrum disorders: a meta-analysis of twin studies.
Beata Tick, Patrick Bolton, Francesca Happé, Michael Rutter, Frühling Rijsdijk. J Child Psychol Psychiatry 2016
376
33

Modeling dopamine dysfunction in autism spectrum disorder: From invertebrates to vertebrates.
Gabriella E DiCarlo, Mark T Wallace. Neurosci Biobehav Rev 2022
4
33

Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model.
Denise Haslinger, Regina Waltes, Afsheen Yousaf, Silvia Lindlar, Ines Schneider, Chai K Lim, Meng-Miao Tsai, Boyan K Garvalov, Amparo Acker-Palmer, Nicolas Krezdorn,[...]. Mol Autism 2018
24
33

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
780
33

The pediatric psychopharmacology of autism spectrum disorder: A systematic review - Part I: The past and the present.
Antonio M Persico, Arianna Ricciardello, Marco Lamberti, Laura Turriziani, Francesca Cucinotta, Claudia Brogna, Benedetto Vitiello, Celso Arango. Prog Neuropsychopharmacol Biol Psychiatry 2021
21
33


The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisation.
Tony Charman, Eva Loth, Julian Tillmann, Daisy Crawley, Caroline Wooldridge, David Goyard, Jumana Ahmad, Bonnie Auyeung, Sara Ambrosino, Tobias Banaschewski,[...]. Mol Autism 2017
85
33

Development of a patient-centered conceptual model of the impact of living with autism spectrum disorder.
Fiona McDougall, Thomas Willgoss, Steve Hwang, Federico Bolognani, Lorraine Murtagh, Evdokia Anagnostou, Diana Rofail. Autism 2018
4
33

Insufficient Evidence for "Autism-Specific" Genes.
Scott M Myers, Thomas D Challman, Raphael Bernier, Thomas Bourgeron, Wendy K Chung, John N Constantino, Evan E Eichler, Sebastien Jacquemont, David T Miller, Kevin J Mitchell,[...]. Am J Hum Genet 2020
64
33

Genetic causes of developmental disorders.
Jacob A S Vorstman, Roel A Ophoff. Curr Opin Neurol 2013
45
33

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.
Simon G Gregory, Jessica J Connelly, Aaron J Towers, Jessica Johnson, Dhani Biscocho, Christina A Markunas, Carla Lintas, Ruth K Abramson, Harry H Wright, Peter Ellis,[...]. BMC Med 2009
377
33

A framework for an evidence-based gene list relevant to autism spectrum disorder.
Christian P Schaaf, Catalina Betancur, Ryan K C Yuen, Jeremy R Parr, David H Skuse, Louise Gallagher, Raphael A Bernier, Janet A Buchanan, Joseph D Buxbaum, Chun-An Chen,[...]. Nat Rev Genet 2020
43
33

Arbaclofen in fragile X syndrome: results of phase 3 trials.
Elizabeth Berry-Kravis, Randi Hagerman, Jeannie Visootsak, Dejan Budimirovic, Walter E Kaufmann, Maryann Cherubini, Peter Zarevics, Karen Walton-Bowen, Paul Wang, Mark F Bear,[...]. J Neurodev Disord 2017
101
33

Synaptic E-I Balance Underlies Efficient Neural Coding.
Shanglin Zhou, Yuguo Yu. Front Neurosci 2018
62
33

Human mini-brain models.
Hsih-Yin Tan, Hansang Cho, Luke P Lee. Nat Biomed Eng 2021
24
33

Behavioral, cognitive, and adaptive development in infants with autism spectrum disorder in the first 2 years of life.
Annette Estes, Lonnie Zwaigenbaum, Hongbin Gu, Tanya St John, Sarah Paterson, Jed T Elison, Heather Hazlett, Kelly Botteron, Stephen R Dager, Robert T Schultz,[...]. J Neurodev Disord 2015
162
33

Synaptic and transcriptionally downregulated genes are associated with cortical thickness differences in autism.
Rafael Romero-Garcia, Varun Warrier, Edward T Bullmore, Simon Baron-Cohen, Richard A I Bethlehem. Mol Psychiatry 2019
64
33

From early markers to neuro-developmental mechanisms of autism.
T Gliga, E J H Jones, R Bedford, T Charman, M H Johnson. Dev Rev 2014
71
33

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Robert W Davies, Ania M Fiksinski, Elemi J Breetvelt, Nigel M Williams, Stephen R Hooper, Thomas Monfeuga, Anne S Bassett, Michael J Owen, Raquel E Gur, Bernice E Morrow,[...]. Nat Med 2020
48
33

Mavoglurant in fragile X syndrome: Results of two randomized, double-blind, placebo-controlled trials.
Elizabeth Berry-Kravis, Vincent Des Portes, Randi Hagerman, Sébastien Jacquemont, Perrine Charles, Jeannie Visootsak, Marc Brinkman, Karin Rerat, Barbara Koumaras, Liansheng Zhu,[...]. Sci Transl Med 2016
166
33


Peripheral Mechanosensory Neuron Dysfunction Underlies Tactile and Behavioral Deficits in Mouse Models of ASDs.
Lauren L Orefice, Amanda L Zimmerman, Anda M Chirila, Steven J Sleboda, Joshua P Head, David D Ginty. Cell 2016
180
33

Autistic traits and abnormal sensory experiences in adults.
Jamie Horder, C Ellie Wilson, M Andreina Mendez, Declan G Murphy. J Autism Dev Disord 2014
85
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.