Cindy Skinner

7.5k total citations
64 papers, 2.5k citations indexed

About

Cindy Skinner is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Cindy Skinner has authored 64 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 39 papers in Molecular Biology and 20 papers in Cognitive Neuroscience. Recurrent topics in Cindy Skinner's work include Genetics and Neurodevelopmental Disorders (42 papers), Autism Spectrum Disorder Research (20 papers) and Genomic variations and chromosomal abnormalities (18 papers). Cindy Skinner is often cited by papers focused on Genetics and Neurodevelopmental Disorders (42 papers), Autism Spectrum Disorder Research (20 papers) and Genomic variations and chromosomal abnormalities (18 papers). Cindy Skinner collaborates with scholars based in United States, Canada and Australia. Cindy Skinner's co-authors include Charles E. Schwartz, Roger E. Stevenson, Richard J. Schroer, Richard J. Simensen, Steve S. Sommer, Jinong Feng, Yan Jin, Luigi Boccuto, Steven A. Skinner and Ron C. Michaelis and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Cindy Skinner

62 papers receiving 2.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Cindy Skinner United States	25	1.6k	1.4k	907	257	134	64	2.5k
Amélie Piton France	21	1.3k 0.8×	1.4k 1.0×	468 0.5×	328 1.3×	109 0.8×	48	2.6k
Peter Huppke Germany	26	2.0k 1.2×	1.2k 0.9×	1.3k 1.5×	152 0.6×	55 0.4×	52	2.8k
Frédéric Laumonnier France	19	1.0k 0.6×	1.1k 0.8×	653 0.7×	343 1.3×	71 0.5×	42	1.9k
Paolo Moretti United States	15	1.0k 0.6×	1.6k 1.1×	665 0.7×	293 1.1×	64 0.5×	35	2.5k
Yuji Kajiwara United States	22	747 0.5×	997 0.7×	636 0.7×	367 1.4×	77 0.6×	46	2.2k
Mojgan Rastegar Canada	35	1.1k 0.7×	1.7k 1.2×	377 0.4×	194 0.8×	254 1.9×	69	2.8k
Steven D. Sheridan United States	22	736 0.5×	1.5k 1.1×	374 0.4×	356 1.4×	68 0.5×	43	2.6k
Mona D. Shahbazian United States	11	1.5k 1.0×	2.3k 1.6×	877 1.0×	180 0.7×	64 0.5×	12	3.1k
Richard J. Schroer United States	24	1.3k 0.8×	976 0.7×	795 0.9×	208 0.8×	228 1.7×	39	2.0k
Philip J. Ebert United States	22	634 0.4×	1.1k 0.8×	571 0.6×	454 1.8×	56 0.4×	36	2.3k

Countries citing papers authored by Cindy Skinner

Since Specialization

Citations

This map shows the geographic impact of Cindy Skinner's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Cindy Skinner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cindy Skinner more than expected).

Fields of papers citing papers by Cindy Skinner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cindy Skinner. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Cindy Skinner. The network helps show where Cindy Skinner may publish in the future.

Co-authorship network of co-authors of Cindy Skinner

This figure shows the co-authorship network connecting the top 25 collaborators of Cindy Skinner. A scholar is included among the top collaborators of Cindy Skinner based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Cindy Skinner. Cindy Skinner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Sahajpal, Nikhil, Jane H. Dean, Benjamin Hilton, et al.. (2025). Optical genome mapping identifies rare structural variants in neural tube defects. Genome Research. 35(4). 798–809.

Broeckel, Ulrich, M. Anwar Iqbal, Brynn Levy, et al.. (2024). Detection of Constitutional Structural Variants by Optical Genome Mapping. Journal of Molecular Diagnostics. 26(3). 213–226. 8 indexed citations

Alesi, Viola, Charles E. Schwartz, Cindy Skinner, et al.. (2024). PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports. Frontiers in Psychiatry. 14. 1327802–1327802. 1 indexed citations

Oberman, Lindsay M., Sujata Srikanth, Kelly L. Jones, et al.. (2023). Sleep disturbances in Phelan‐McDermid syndrome: Clinical and metabolic profiling of 56 individuals. Clinical Genetics. 104(2). 198–209. 2 indexed citations

Oberman, Lindsay M., Melanie May, Sujata Srikanth, et al.. (2021). Genetic and metabolic profiling of individuals with Phelan‐McDermid syndrome presenting with seizures. Clinical Genetics. 101(1). 87–100. 13 indexed citations

Wang, Wei, Sarah L. Fordyce Martin, Diana L. Bordin, et al.. (2021). Increased p53 signaling impairs neural differentiation in HUWE1-promoted intellectual disabilities. Cell Reports Medicine. 2(4). 100240–100240. 5 indexed citations

Haghshenas, Sadegheh, Michael A. Levy, Jennifer Kerkhof, et al.. (2021). Detection of a DNA Methylation Signature for the Intellectual Developmental Disorder, X-Linked, Syndromic, Armfield Type. International Journal of Molecular Sciences. 22(3). 1111–1111. 6 indexed citations

Louie, Raymond J., Debra L. Collins, Michael J. Friez, et al.. (2020). Schimke XLID syndrome results from a deletion in BCAP31. American Journal of Medical Genetics Part A. 182(9). 2168–2174. 7 indexed citations

Niranjan, Tejasvi, Melanie May, Patrick Tarpey, et al.. (2019). Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders. Molecular Genetics & Genomic Medicine. 7(4). e00569–e00569. 10 indexed citations

10.

Aref‐Eshghi, Erfan, David I. Rodenhiser, Laila C. Schenkel, et al.. (2018). Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes. The American Journal of Human Genetics. 102(1). 156–174. 90 indexed citations

11.

Schenkel, Laila C., Kristin D. Kernohan, Arran McBride, et al.. (2017). Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome. Epigenetics & Chromatin. 10(1). 10–10. 42 indexed citations

12.

Hashimoto, Satoru, Melanie May, Alexey Epanchintsev, et al.. (2017). MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression. Human Molecular Genetics. 26(11). 2062–2075. 17 indexed citations

13.

Aref‐Eshghi, Erfan, Laila C. Schenkel, Hanxin Lin, et al.. (2017). Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders. Journal of Molecular Diagnostics. 19(6). 848–856. 26 indexed citations

14.

Godler, David E., Y. Inaba, Cindy Skinner, et al.. (2013). Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and puberty. Human Molecular Genetics. 22(8). 1516–1524. 19 indexed citations

15.

Grafodatskaya, Daria, Darci T. Butcher, Andrei L. Turinsky, et al.. (2013). Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C. BMC Medical Genomics. 6(1). 1–1. 68 indexed citations

16.

Boccuto, Luigi, Sara M. Sarasua, Cindy Skinner, et al.. (2012). Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. European Journal of Human Genetics. 21(3). 310–316. 176 indexed citations

17.

Mefford, Heather C, Gregory M. Cooper, Troy Zerr, et al.. (2009). A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease. Genome Research. 19(9). 1579–1585. 101 indexed citations

18.

Feng, Jinong, Richard J. Schroer, Yan Jin, et al.. (2006). High frequency of neurexin 1β signal peptide structural variants in patients with autism. Neuroscience Letters. 409(1). 10–13. 219 indexed citations

19.

Michaelis, Ron C., Khalid Sossey‐Alaoui, Cindy Skinner, et al.. (2000). The HOPA Gene Dodecamer Duplication Is Not a Significant Etiological Factor in Autism. Journal of Autism and Developmental Disorders. 30(4). 355–358. 9 indexed citations

20.

Schroer, Richard J., Mary C. Phelan, Ron C. Michaelis, et al.. (1998). Autism and maternally derived aberrations of chromosome 15q. American Journal of Medical Genetics. 76(4). 327–336. 284 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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