Charles E. Schwartz

27.3k total citations · 1 hit paper
319 papers, 13.0k citations indexed

About

Charles E. Schwartz is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Charles E. Schwartz has authored 319 papers receiving a total of 13.0k indexed citations (citations by other indexed papers that have themselves been cited), including 206 papers in Molecular Biology, 193 papers in Genetics and 38 papers in Cognitive Neuroscience. Recurrent topics in Charles E. Schwartz's work include Genetics and Neurodevelopmental Disorders (151 papers), Genomic variations and chromosomal abnormalities (41 papers) and Autism Spectrum Disorder Research (38 papers). Charles E. Schwartz is often cited by papers focused on Genetics and Neurodevelopmental Disorders (151 papers), Genomic variations and chromosomal abnormalities (41 papers) and Autism Spectrum Disorder Research (38 papers). Charles E. Schwartz collaborates with scholars based in United States, Canada and Australia. Charles E. Schwartz's co-authors include Roger E. Stevenson, Herbert A. Lubs, Cindy Skinner, Anand K. Srivastava, Melanie May, Giovanni Neri, Huntington F. Willard, Richard J. Simensen, Robert M. Plenge and Michael J. Friez and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Charles E. Schwartz

315 papers receiving 12.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

AGTR2 Mutations in X-Linked Mental Retardation

2002 521 citations Virginie Vervoort, Sydney Ladd et al. Science profile →

Peers

Countries citing papers authored by Charles E. Schwartz

Since Specialization

Citations

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

Fields of papers citing papers by Charles E. Schwartz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles E. Schwartz. 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 Charles E. Schwartz. The network helps show where Charles E. Schwartz may publish in the future.

Co-authorship network of co-authors of Charles E. Schwartz

This figure shows the co-authorship network connecting the top 25 collaborators of Charles E. Schwartz. A scholar is included among the top collaborators of Charles E. Schwartz 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 Charles E. Schwartz. Charles E. Schwartz 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

#	Work	Indexed citations
1	Expanding allelic and phenotypic spectrum of ZC4H2‐related disorder: A novel hypomorphic variant and high prevalence of tethered cord 2022 ·Clinical Genetics ·Parith Wongkittichote, Tae‐Ik Choi, (unknown), (unknown), Dwight D. Koeberl, Vinodh Narayanan, Keri Ramsey, Chris Balak, Charles E. Schwartz, Anna M. Cueto‐González, Francina Munell, Cheol‐Hee Kim, Marwan Shinawi	5
2	Increased p53 signaling impairs neural differentiation in HUWE1-promoted intellectual disabilities 2021 ·Cell Reports Medicine ·(unknown), (unknown), (unknown), (unknown), Wei Wang, (unknown), (unknown), (unknown), Sarah L. Fordyce Martin, Diana L. Bordin, Matthias Bosshard, Yunhui Peng, Emil Alexov, Cindy Skinner, Nina‐Beate Liabakk, Gareth J. Sullivan, Magnar Bjørås, Charles E. Schwartz, Barbara van Loon	5
3	Detection of a DNA Methylation Signature for the Intellectual Developmental Disorder, X-Linked, Syndromic, Armfield Type 2021 ·International Journal of Molecular Sciences ·Sadegheh Haghshenas, Michael A. Levy, Jennifer Kerkhof, Erfan Aref‐Eshghi, Haley McConkey, Tuğçe B. Balcı, Victoria Mok Siu, Cindy Skinner, Roger E. Stevenson, Bekim Sadiković, Charles E. Schwartz	6
4	The complete loss of function of the SMS gene results in a severe form of Snyder-Robinson syndrome 2019 ·European Journal of Medical Genetics ·Lise Larcher, Joy Norris, (unknown), Julien Buratti, Cyril Mignot, Cathérine Garel, Boris Keren, Charles E. Schwartz, Sandra Whalen	21
5	Polyamine Homeostasis in Snyder-Robinson Syndrome 2018 ·SHILAP Revista de lepidopterología ·Tracy Murray Stewart, Matthew Dunworth, Jackson R. Foley, Charles E. Schwartz, Robert A. Casero	32
6	Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome 2017 ·Epigenetics & Chromatin ·Laila C. Schenkel, Kristin D. Kernohan, Arran McBride, (unknown), Amanda Hodge, Peter Ainsworth, David I. Rodenhiser, Guillaume Paré, Nathalie G. Bérubé, Cindy Skinner, Kym M. Boycott, Charles E. Schwartz, Bekim Sadiković	42
7	MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression 2017 ·Human Molecular Genetics ·(unknown), (unknown), Satoru Hashimoto, Melanie May, Alexey Epanchintsev, Colm J. Ryan, William Allen, Anna Hackett, Jozef Gécz, Cindy Skinner, Roger E. Stevenson, Arjan P.M. de Brouwer, Charles Coutton, Christine Francannet, Pierre‐Simon Jouk, Charles E. Schwartz, Jean‐Marc Egly	17
8	MED12 related disorders 2013 ·American Journal of Medical Genetics Part A ·John M. Graham, Charles E. Schwartz	53
9	A Y328C missense mutation in spermine synthase causes a mild form of Snyder–Robinson syndrome 2013 ·Human Molecular Genetics ·Zhe Zhang, Joy Norris, Vera M. Kalscheuer, Tim Wood, Lin Wang, Charles E. Schwartz, Emil Alexov, Hilde Van Esch	31
10	Spermine Synthase Deficiency Resulting in X-Linked Intellectual Disability (Snyder–Robinson Syndrome) 2011 ·Methods in molecular biology ·Charles E. Schwartz, (unknown), Roger E. Stevenson, Anthony E. Pegg	28
11	Characterization of novel SLC6A8 variants with the use of splice-site analysis tools and implementation of a newly developed LOVD database 2010 ·European Journal of Human Genetics ·(unknown), Efraim H. Rosenberg, Lígia S. Almeida, Tjitske Kleefstra, Charles E. Schwartz, Vassili Valayannopoulos, Omar Abdul‐Rahman, Nicola Poplawski, Laura Vilarinho, Philipp Wolf, Johan T. den Dunnen, Cornelis Jakobs, Gajja S. Salomons	15
12	Intellectual disability, midface hypoplasia, facial hypotonia, and alport syndrome are associated with a deletion in Xq22.3 2010 ·American Journal of Medical Genetics Part A ·Jayson Rodriguez, (unknown), Ilaria Meloni, Sydney Ladd, Nancy D. Leslie, (unknown), Alessandra Renieri, Barbara R. DuPont, Roger E. Stevenson, Charles E. Schwartz, Anand K. Srivastava	13
13	A missense mutation, p.V132G, in the X‐linked spermine synthase gene (SMS) causes Snyder–Robinson syndrome 2009 ·American Journal of Medical Genetics Part A ·(unknown), J. Butler, (unknown), Diane E. McCloskey, (unknown), Anthony E. Pegg, Charles E. Schwartz, José Sánchez‐Corona, José Elías García‐Ortíz	48
14	Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia 2008 ·Journal of Medical Genetics ·Fatima Abidi, (unknown), (unknown), David D. Weaver, Richard J. Simensen, Roger E. Stevenson, R. Curtis Rogers, Charles E. Schwartz	76
15	Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair 2008 ·Genome Research ·Marijke Bauters, Hilde Van Esch, Michael J. Friez, Odile Boespflug‐Tanguy, Martin Zenker, Angela Maria Vianna‐Morgante, Carla Rosenberg, Jaakko Ignatius, Martine Raynaud, Karen Hollanders, Karen Govaerts, (unknown), Florence Niel, Pierre Blanc, Roger E. Stevenson, Jean‐Pierre Fryns, Peter Marynen, Charles E. Schwartz, Guy Froyen	92
16	XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene 2005 ·BMC Medical Genetics ·(unknown), (unknown), Merran Finnis, Marie Mangelsdorf, Elke Holinski‐Feder, (unknown), Andrée MacMillan, (unknown), Jozef Gécz, Roger E. Stevenson, Charles E. Schwartz	23
17	Shashi XLMR syndrome: Report of a second family 2003 ·American Journal of Medical Genetics Part A ·(unknown), Rita de Cássia Stocco, (unknown), Willy Beçak, (unknown), C.J. Lindsey, Herbert A. Lubs, Roger E. Stevenson, Charles E. Schwartz	8
18	AGTR2 Mutations in X-Linked Mental Retardation breakdown → 2002 ·Science ·Virginie Vervoort, (unknown), (unknown), Sydney Ladd, (unknown), (unknown), Katie Clarkson, Barbara R. DuPont, Charles E. Schwartz, Roger E. Stevenson, (unknown), Anand K. Srivastava	521
19	Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1 1998 ·Human Molecular Genetics ·Chris Gunter, William Paradee, Dana C. Crawford, (unknown), Jane Newman, Catherine B. Kunst, David L. Nelson, Charles E. Schwartz, Anna Murray, John MacPherson, S. L. Sherman, Stephen T. Warren	59
20	Localization to Xq22 and clinical update of a family with X-linked recessive mental retardation with progression sensorineural deafness, progressive tapeto-retinal degeneration and dystonia 1994 ·American Journal of Medical Genetics Part A ·Lisbeth Tranebjærg, Charles E. Schwartz, (unknown), David Barker, (unknown), J. Fernando Arena, Tobias Gedde‐Dahl, Margareta Mikkelsen, Svein Ivar Mellgren, Karen E. Anderson	1

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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