Mary Leslie

505 total citations
9 papers, 388 citations indexed

About

Mary Leslie is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Mary Leslie has authored 9 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Cognitive Neuroscience and 3 papers in Molecular Biology. Recurrent topics in Mary Leslie's work include Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (3 papers). Mary Leslie is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (3 papers). Mary Leslie collaborates with scholars based in United States. Mary Leslie's co-authors include Stephanie L. Sherman, Elizabeth Scott, Ann Abramowitz, Dana C. Crawford, Emily G. Allen, Debra Hamilton, Lisa Shubeck, Krista Charen, Jessica Ezzell Hunter and Amy K. Sullivan and has published in prestigious journals such as The American Journal of Human Genetics, Behavior Genetics and American Journal of Medical Genetics.

In The Last Decade

Mary Leslie

9 papers receiving 378 citations

Peers

Countries citing papers authored by Mary Leslie

Since Specialization

Citations

This map shows the geographic impact of Mary Leslie'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 Mary Leslie with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mary Leslie more than expected).

Fields of papers citing papers by Mary Leslie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary Leslie. 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 Mary Leslie. The network helps show where Mary Leslie may publish in the future.

Co-authorship network of co-authors of Mary Leslie

This figure shows the co-authorship network connecting the top 25 collaborators of Mary Leslie. A scholar is included among the top collaborators of Mary Leslie 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 Mary Leslie. Mary Leslie is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	Acquisition of Letter Naming Knowledge, Phonological Awareness, and Spelling Knowledge of Kindergarten Children at Risk for Learning to Read 2018 ·David D. Paige, William H. Rupley, (unknown), (unknown), Mary Leslie	23
2	Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms 2012 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Jessica Ezzell Hunter, Mary Leslie, (unknown), Debra Hamilton, Lisa Shubeck, Krista Charen, Ann Abramowitz, Michael P. Epstein, Adriana Lori, Elisabeth B. Binder, Joseph F. Cubells, Stephanie L. Sherman	32
3	No Evidence for a Difference in Neuropsychological Profile among Carriers and Noncarriers of the FMR1 Premutation in Adults under the Age of 50 2008 ·The American Journal of Human Genetics ·Jessica Ezzell Hunter, Emily G. Allen, Ann Abramowitz, (unknown), Mary Leslie, (unknown), Debra Hamilton, Lisa Shubeck, Krista Charen, Stephanie L. Sherman	61
4	Investigation of Phenotypes Associated with Mood and Anxiety Among Male and Female Fragile X Premutation Carriers 2008 ·Behavior Genetics ·Jessica Ezzell Hunter, Emily G. Allen, Ann Abramowitz, (unknown), Mary Leslie, (unknown), Debra Hamilton, Lisa Shubeck, Krista Charen, Stephanie L. Sherman	52
5	Examination of the Effect of the Polymorphic CGG Repeat in the FMR1 Gene on Cognitive Performance 2005 ·Behavior Genetics ·Emily G. Allen, Stephanie L. Sherman, Ann Abramowitz, Mary Leslie, (unknown), (unknown), Elizabeth Scott, Richard Letz	40
6	A Creative Model for a Post-Treatment Group for Women With Cancer 2003 ·Canadian Journal of Counselling and Psychotherapy ·(unknown), Mary Leslie	1
7	Paternally Transmitted FMR1 Alleles Are Less Stable than Maternally Transmitted Alleles in the Common and Intermediate Size Range 2002 ·The American Journal of Human Genetics ·Amy K. Sullivan, Dana C. Crawford, Elizabeth Scott, Mary Leslie, Stephanie L. Sherman	53
8	Prevalence of the fragile X syndrome in African‐Americans 2002 ·American Journal of Medical Genetics ·Dana C. Crawford, Kellen L. Meadows, James L. Newman, Lisa F. Taft, Elizabeth Scott, Mary Leslie, (unknown), Patricia Holmgreen, Marshalyn Yeargin‐Allsopp, Coleen Boyle, Stephanie L. Sherman	113
9	Cognitive and behavioral performance among FMR1 high‐repeat allele carriers surveyed from special education classes 2002 ·American Journal of Medical Genetics ·Stephanie L. Sherman, Frederick Marsteller, Ann Abramowitz, Elizabeth Scott, Mary Leslie, Joel D. Bregman	13

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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