CE Schwartz

995 total citations
22 papers, 617 citations indexed

About

CE Schwartz is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, CE Schwartz has authored 22 papers receiving a total of 617 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 15 papers in Genetics and 2 papers in Surgery. Recurrent topics in CE Schwartz's work include Genetics and Neurodevelopmental Disorders (13 papers), Ubiquitin and proteasome pathways (4 papers) and RNA regulation and disease (3 papers). CE Schwartz is often cited by papers focused on Genetics and Neurodevelopmental Disorders (13 papers), Ubiquitin and proteasome pathways (4 papers) and RNA regulation and disease (3 papers). CE Schwartz collaborates with scholars based in United States, France and South Africa. CE Schwartz's co-authors include Roger E. Stevenson, Maria Giuseppina Miano, JC Murray, Mark H. Skolnick, L.A. Menlove, Curtis L. Atkin, Sandra J. Hasstedt, Lisa A. Cannon, K. Nguyen and C. H. van der Meyden and has published in prestigious journals such as Nucleic Acids Research, JNCI Journal of the National Cancer Institute and Journal of Psychosomatic Research.

In The Last Decade

CE Schwartz

22 papers receiving 603 citations

Peers

Countries citing papers authored by CE Schwartz

Since Specialization

Citations

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

Fields of papers citing papers by CE Schwartz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of CE Schwartz

This figure shows the co-authorship network connecting the top 25 collaborators of CE Schwartz. A scholar is included among the top collaborators of CE 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 CE Schwartz. CE 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	Two percent of patients suspected of having Angelman syndrome have TCF4 mutations 2010 ·Clinical Genetics ·Kyoko Takano, Michael J. Lyons, C. D. Moyes, Julie R. Jones, CE Schwartz	40
2	ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal 2009 ·BMJ Case Reports ·Elysa J. Marco, Fatima Abidi, James Bristow, (unknown), Philip D. Cotter, Rita J. Jeremy, CE Schwartz, Elliott H. Sherr	5
3	A novel mutation in the PHF8 gene is associated with X‐linked mental retardation with cleft lip/cleft palate 2007 ·Clinical Genetics ·(unknown), Maria Giuseppina Miano, JC Murray, CE Schwartz	83
4	Expanding the phenotypic spectrum of L1CAM‐associated disease 2006 ·Clinical Genetics ·Lina Basel‐Vanagaite, Rachel Straussberg, (unknown), Dov Inbar, (unknown), M Shohat, CE Schwartz	25
5	High prevalence of SLC6A8 deficiency, a novel X-linked mental retardation syndrome 2005 ·Molecular Genetics and Metabolism ·(unknown), Tjitske Kleefstra, Trevor Wood, Leonardo Almeida, (unknown), (unknown), (unknown), (unknown), (unknown), Claude Moraine, (unknown), Jean‐Pierre Fryns, (unknown), (unknown), CE Schwartz, (unknown)	1
6	OPD-spectrum Disorders Clinical Collaborative Group. Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans 2003 ·Lirias (KU Leuven) ·(unknown), (unknown), (unknown), (unknown), R J Gorlin, David Horn, (unknown), (unknown), Éva Morava, Ruth Newbury‐Ecob, (unknown), (unknown), CE Schwartz, (unknown), Mohnish Suri, John Kendrick‐Jones, Andrew O.M. Wilkie	34
7	Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation 2002 ·Journal of Medical Genetics ·Anne-Marie Lossi, (unknown), D. Depétris, Jozef Gécz, Ági K. Gedeon, R. Frank Kooy, CE Schwartz, Marie‐Geneviève Mattéi, M. F. Croquette, Laurent Villard	23
8	Non‐syndromic X‐linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene 2002 ·Clinical Genetics ·R. David Lebel, Melanie May, (unknown), (unknown), (unknown), CE Schwartz	61
9	Cognitive function in Coffin–Lowry syndrome 2002 ·Clinical Genetics ·(unknown), Fatima Abidi, (unknown), CE Schwartz, (unknown)	14
10	Clinical and molecular contributions to the understanding of X-linked mental retardation 2002 ·Cytogenetic and Genome Research ·Roger E. Stevenson, CE Schwartz	33
11	Penetrance of Mutations in the Familial Wilms Tumor Gene FWT1 2000 ·JNCI Journal of the National Cancer Institute ·Nazneen Rahman, Laura Arbour, Richard S. Houlston, Catherine Bonaïti‐Pellié, Fatima Abidi, (unknown), Deborah Ford, Steven A. Narod, Kathy Pritchard‐Jones, William D. Foulkes, CE Schwartz, Michael R. Stratton	8
12	X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27 1999 ·Journal of Medical Genetics ·Arnold L. Christianson, Roger E. Stevenson, C. H. van der Meyden, (unknown), (unknown), (unknown), (unknown), CE Schwartz	88
13	A family with mental retardation, variable macrocephaly and macro-orchidism, and linkage to Xq12-q21. 1998 ·Journal of Medical Genetics ·John P. Johnson, (unknown), CE Schwartz	8
14	A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28. 1997 ·Journal of Medical Genetics ·G. Shashidhar Pai, (unknown), Maries Joseph, (unknown), (unknown), J. Fernando Arena, Herbert A. Lubs, Roger E. Stevenson, CE Schwartz	25
15	Maternal expressed emotion and parental affective disorder : risk for childhood depressive disorder, substance abuse or conduct disorder 1990 ·Journal of Psychosomatic Research ·CE Schwartz	1
16	New TaqI RFLPs at the DXS52 (St14) locus in the black population 1989 ·Nucleic Acids Research ·(unknown), CE Schwartz	2
17	Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXA 1989 ·Cytogenetic and Genome Research ·(unknown), (unknown), C.-L. Richer, CE Schwartz	2
18	Mapping of Alport syndrome to the long arm of the X chromosome. 1988 ·PubMed ·Curtis L. Atkin, Sandra J. Hasstedt, L.A. Menlove, Lisa A. Cannon, (unknown), CE Schwartz, K. Nguyen, Mark H. Skolnick	95
19	Relationships between the human pepsinogen DNA and protein polymorphisms. 1986 ·PubMed ·R.T. Taggart, I. Michael Samloff, Leslie J. Raffel, (unknown), (unknown), Gloria M. Petersen, Jerome I. Rotter, Mark H. Skolnick, CE Schwartz, G I Bell	20
20	Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene. 1985 ·PubMed ·S.C. Bock, John F. Harris, CE Schwartz, John H. Ward, E. J. Hershgold, Mark H. Skolnick	27

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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