Christine J. Shaw

1.3k citations

14 papers · 913 indexed · h-index 13

Genetics top 2%
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 2
Genetics top 10%
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 2
Plant Science top 10%
- Chromosomal and Genetic Variations 7
Molecular Biology
- Genomics and Chromatin Dynamics 3
- Congenital heart defects research 2
- Chromatin Remodeling and Cancer 2
- RNA and protein synthesis mechanisms 2
Developmental Neuroscience
Developmental Biology
- Congenital limb and hand anomalies 2

Co-authors: James R. Lupski Paweł Stankiewicz Marjorie Withers Weimin Bi Sung Sup Park Lorraine Potocki Ken Inoue Lisa G. Shaffer
Cited by: Genetics Plant Science
Journals: Molecular Cell (1 paper)Genome Research (2 papers)The American Journal of Human Genetics (4 papers)
Partner nations: United States Australia Netherlands

In The Last Decade

Christine J. Shaw

14 papers receiving 892 citations

Peers

Countries citing papers authored by Christine J. Shaw

Since Specialization

Citations

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

Fields of papers citing papers by Christine J. Shaw

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christine J. Shaw. 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 Christine J. Shaw. The network helps show where Christine J. Shaw may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Christine J. Shaw, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Christine J. Shaw Line = papers co-authored together Christine J. Shaw links everyone, so they are left out of the graph.

All Works

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14 of 14 papers shown

#	Work
1	Platform comparison of detecting copy number variants with microarrays and whole-exome sequencing Genomics Data ·Joep de Ligt,Philip M. Boone,Rolph Pfundt,Lisenka E.L.M. Vissers,Nicole de Leeuw,Christine J. Shaw,Han G. Brunner,James R. Lupski,Joris A. Veltman,Jayne Y. Hehir‐Kwa	2014	13
2	Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing Human Mutation ·Joep de Ligt,Philip M. Boone,Rolph Pfundt,Lisenka E.L.M. Vissers,Todd Richmond,Joel Geoghegan,Kathleen O’Moore,Nicole de Leeuw,Christine J. Shaw,Han G. Brunner,James R. Lupski,Joris A. Veltman,Jayne Y. Hehir‐Kwa	2013	79
3	Uncommon Deletions of the Smith-Magenis Syndrome Region Can Be Recurrent When Alternate Low-Copy Repeats Act as Homologous Recombination Substrates The American Journal of Human Genetics ·Christine J. Shaw,Marjorie Withers,James R. Lupski	2004	46
4	Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms Human Genetics ·Christine J. Shaw,James R. Lupski	2004	81
5	Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome Human Genetics ·Weimin Bi,Gulam Mustafa Saifi,Christine J. Shaw,Katherina Walz,Patricia Fonseca,Meredith Wilson,Lorraine Potocki,James R. Lupski	2004	81
6	Serial segmental duplications during primate evolution result in complex human genome architecture Genome Research ·Paweł Stankiewicz,Christine J. Shaw,Marjorie Withers,Ken Inoue,James R. Lupski	2004	87
7	Small marker chromosomes in two patients with segmental aneusomy for proximal 17p Human Genetics ·Marta Carrera,Christine J. Shaw,Pawel Stankiewicz,Gabriel A. Bien‐Willner,Scott C. Bello,Luis Pérez Jurado,Xavier Estivill,James R. Lupski,Chad A. Shaw	2004	19
8	Genome Architecture Catalyzes Nonrecurrent Chromosomal Rearrangements The American Journal of Human Genetics ·Paweł Stankiewicz,Christine J. Shaw,Jason Dapper,Keiko Wakui,Lisa G. Shaffer,Marjorie Withers,Leah I. Elizondo,Sung Sup Park,James R. Lupski	2003	144
9	Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)] Genetics in Medicine ·Lorraine Potocki,Christine J. Shaw,Paweł Stankiewicz,James R. Lupski	2003	80
10	Arm Sequences Contribute to the Architecture and Catalytic Function of a λ Integrase-Holliday Junction Complex Molecular Cell ·Marta Radman‐Livaja,Christine J. Shaw,Marco A. Azaro,Tapan Biswas,Tom Ellenberger,Arthur Landy	2003	27
11	A girl with duplication 17p10‐p12 associated with a dicentric chromosome American Journal of Medical Genetics Part A ·Christine J. Shaw,Paweł Stankiewicz,John Christodoulou,Ellie Smith,Kristi Jones,James R. Lupski	2003	8
12	Reciprocal Crossovers and a Positional Preference for Strand Exchange in Recombination Events Resulting in Deletion or Duplication of Chromosome 17p11.2 The American Journal of Human Genetics ·Weimin Bi,Sung Sup Park,Christine J. Shaw,Marjorie Withers,Pragna I. Patel,James R. Lupski	2003	94
13	Genetic Proof of Unequal Meiotic Crossovers in Reciprocal Deletion and Duplication of 17p11.2 The American Journal of Human Genetics ·Christine J. Shaw,Weimin Bi,James R. Lupski	2002	68
14	Structure and Evolution of the Smith-Magenis Syndrome Repeat Gene Clusters, SMS-REPs Genome Research ·Sung Sup Park,Paweł Stankiewicz,Weimin Bi,Christine J. Shaw,Jessica A. Lehoczky,Ken Dewar,Bruce W. Birren,James R. Lupski	2002	86

About Christine J. Shaw

Christine J. Shaw is a scholar working on Developmental Biology, Genetics and Plant Science, having authored 14 papers that have together received 913 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (7 papers), Genomics and Chromatin Dynamics (3 papers), Genomics and Rare Diseases (2 papers), Congenital limb and hand anomalies (2 papers), Congenital heart defects research (2 papers), Chromatin Remodeling and Cancer (2 papers) and RNA and protein synthesis mechanisms (2 papers). The work is most often cited by research in Genetics (746 citations), Genetics (103 citations) and Plant Science (313 citations). Christine J. Shaw has collaborated with scholars based in United States, Australia and Netherlands. Frequent co-authors include James R. Lupski, Paweł Stankiewicz, Marjorie Withers, Weimin Bi, Sung Sup Park, Lorraine Potocki, Ken Inoue, Lisa G. Shaffer, Jason Dapper and Leah I. Elizondo. Their work appears in journals such as Molecular Cell, Genome Research and The American Journal of Human Genetics.

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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