Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Whole Exome Sequencing in Females with Autism Implicates Novel and Candidate Genes
Merlin G. Butler, Syed K. Rafi, Waheeda A. Hossain, et al.
International Journal of Molecular Sciences (2015) Vol. 16, Iss. 1, pp. 1312-1335
Open Access | Times Cited: 89

Showing 1-25 of 89 citing articles:

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders
Siddharth Srivastava, Jamie Love‐Nichols, Kira A. Dies, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 11, pp. 2413-2421
Open Access | Times Cited: 536
Sex Differences in Autism Spectrum Disorder: a Review
Sarah L. Ferri, Ted Abel, Edward S. Brodkin
Current Psychiatry Reports (2018) Vol. 20, Iss. 2
Open Access | Times Cited: 331
Genetic Testing in Neurodevelopmental Disorders
Juliann M. Savatt, Scott M. Myers
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 152
The Autism Spectrum: Behavioral, Psychiatric and Genetic Associations
Ann Genovese, Merlin G. Butler
Genes (2023) Vol. 14, Iss. 3, pp. 677-677
Open Access | Times Cited: 104
Genetics of Autism Spectrum Disorder: Current Status and Possible Clinical Applications
Hee‐Jeong Yoo
Experimental Neurobiology (2015) Vol. 24, Iss. 4, pp. 257-272
Open Access | Times Cited: 154
NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment
Ana Fernández‐Marmiesse, Sofía Gouveia, María L. Couce
Current Medicinal Chemistry (2017) Vol. 25, Iss. 3, pp. 404-432
Open Access | Times Cited: 143
Regulation of neural circuit formation by protocadherins
Stacey L. Peek, Kar Men Mah, Joshua A. Weiner
Cellular and Molecular Life Sciences (2017) Vol. 74, Iss. 22, pp. 4133-4157
Open Access | Times Cited: 119
Regulation of neuronal migration, an emerging topic in autism spectrum disorders
Orly Reiner, Eyal Karzbrun, Aditya Kshirsagar, et al.
Journal of Neurochemistry (2015) Vol. 136, Iss. 3, pp. 440-456
Open Access | Times Cited: 109
Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients
Zhiliang Yang, Ayumi Matsumoto, Kazuhiro Nakayama, et al.
Brain and Development (2015) Vol. 38, Iss. 1, pp. 91-99
Closed Access | Times Cited: 103
Cell adhesion and matricellular support by astrocytes of the tripartite synapse
Anne E.J. Hillen, J. Peter H. Burbach, Elly M. Hol
Progress in Neurobiology (2018) Vol. 165-167, pp. 66-86
Open Access | Times Cited: 101
Proteomics in cerebrospinal fluid and spinal cord suggests UCHL1, MAP2 and GPNMB as biomarkers and underpins importance of transcriptional pathways in amyotrophic lateral sclerosis
Patrick Oeckl, Patrick Weydt, Dietmar Rudolf Thal, et al.
Acta Neuropathologica (2019) Vol. 139, Iss. 1, pp. 119-134
Closed Access | Times Cited: 98
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families
Bashayer Al‐Mubarak, Mohamed Abouelhoda, Aisha Omar, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 90
5p deletions: Current knowledge and future directions
Joanne Nguyen, Krista J. Qualmann, Rebecca A Okashah, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2015) Vol. 169, Iss. 3, pp. 224-238
Open Access | Times Cited: 77
Mitochondrial function and abnormalities implicated in the pathogenesis of ASD
Frank J. Castora
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2018) Vol. 92, pp. 83-108
Closed Access | Times Cited: 76
High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorders
Merlin G. Butler, Syed K. Rafi, Ann M. Manzardo
International Journal of Molecular Sciences (2015) Vol. 16, Iss. 3, pp. 6464-6495
Open Access | Times Cited: 72
ELAVL2-regulated transcriptional and splicing networks in human neurons link neurodevelopment and autism
Stefano Berto, Noriyoshi Usui, Geneviève Konopka, et al.
Human Molecular Genetics (2016), pp. ddw110-ddw110
Open Access | Times Cited: 64
Autism genetics – an overview
Jiani Yin, Christian P. Schaaf
Prenatal Diagnosis (2016) Vol. 37, Iss. 1, pp. 14-30
Closed Access | Times Cited: 62
Abnormal mGluR-mediated synaptic plasticity and autism-like behaviours in Gprasp2 mutant mice
Mohamed Edfawy, Joana R. Guedes, Marta Pereira, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 49
GeneAnalytics Pathways and Profiling of Shared Autism and Cancer Genes
Alexander P. Gabrielli, Ann M. Manzardo, Merlin G. Butler
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 5, pp. 1166-1166
Open Access | Times Cited: 42
Artificial intelligence analysis of newborn leucocyte epigenomic markers for the prediction of autism
Ray Bahado‐Singh, Sangeetha Vishweswaraiah, Buket Aydas, et al.
Brain Research (2019) Vol. 1724, pp. 146457-146457
Closed Access | Times Cited: 38
Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection
Adi Aran, Nuphar Rosenfeld, Ranit Jaron, et al.
Neurology (2016) Vol. 86, Iss. 21, pp. 2016-2024
Open Access | Times Cited: 35
Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing Technology
Elif Funda Şener, Halit Canatan, Yusuf Özkul
Psychiatry Investigation (2016) Vol. 13, Iss. 3, pp. 255-255
Open Access | Times Cited: 35
Comprehensive behavioral phenotyping of a new Semaphorin 3 F mutant mouse
Ikuo Matsuda, Hirotaka Shoji, Nobuyuki Yamasaki, et al.
Molecular Brain (2016) Vol. 9, Iss. 1
Open Access | Times Cited: 32
Right Place at the Right Time: How Changes in Protocadherins Affect Synaptic Connections Contributing to the Etiology of Neurodevelopmental Disorders
Maria Mancini, Silvia Bassani, Maria Passafaro
Cells (2020) Vol. 9, Iss. 12, pp. 2711-2711
Open Access | Times Cited: 28
Semaphorin 3s signaling in the central nervous system: Mechanisms and therapeutic implication for brain diseases
Ya-Ping Lu, Yiling Luo, Zhouyue Wu, et al.
Pharmacology & Therapeutics (2025), pp. 108800-108800
Closed Access
Page 1 - Next Page

Scroll to top