Craig Chinault

3.3k citations

6 papers · 189 indexed · h-index 6

Co-authors: Ankita Patel Sarika U. Peters Marwan Shinawi Trilochan Sahoo Cindy Skinner Steven A. Skinner Bruno Maranda Arthur L. Beaudet
Topics: Genomic variations and chromosomal abnormalities (4 papers)Congenital heart defects research (3 papers)Genetic Syndromes and Imprinting (1 paper)
Cited by: Genetics Sensory Systems Cognitive Neuroscience
Journals: Genome Research Genomics European Journal of Human Genetics
Partner nations: United States Canada Sweden

In The Last Decade

Craig Chinault

6 papers receiving 186 citations

Peers

Countries citing papers authored by Craig Chinault

Since Specialization

Citations

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

Fields of papers citing papers by Craig Chinault

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Craig Chinault

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

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity 2011 ·American Journal of Medical Genetics Part A ·Marwan Shinawi,Trilochan Sahoo,Bruno Maranda,Steven A. Skinner,Cindy Skinner,Craig Chinault,(unknown),Sarika U. Peters,Ankita Patel,Roger E. Stevenson,Arthur L. Beaudet	71
2	Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss 2008 ·European Journal of Human Genetics ·Sandesh C. Sreenath Nagamani,Ayelet Erez,Christine M. Eng,Zhishuo Ou,Craig Chinault,(unknown),James G. Coldwell,Paweł Stankiewicz,Ankita Patel,James R. Lupski,Sau Wai Cheung	39
3	15q13q14 deletions: Phenotypic characterization and molecular delineation by comparative genomic hybridization 2008 ·American Journal of Medical Genetics Part A ·Nicola Brunetti‐Pierri,Trilochan Sahoo,(unknown),Craig Chinault,(unknown),Sau Wai Cheung,Sarika U. Peters,Marwan Shinawi	10
4	A Yeast Artificial Chromosome (YAC) Contig Encompassing the Critical Region of the X-Linked Lymphoproliferative Disease (XLP) Locus 1997 ·Genomics ·Árpád Lányi,(unknown),(unknown),Catherine B. Talmadge,Beda Břicháček,Jack R. Davis,Beth A. Kozel,Barbara J. Trask,Ger van den Engh,É. Uzvölgyi,Eric J. Stanbridge,David L. Nelson,Craig Chinault,Helen E. Heslop,Thomas G. Gross,Thomas A. Seemayer,George Klein,David T. Purtilo,János Sümegi	15
5	Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1. 1996 ·Genome Research ·Radha Ayyagari,Ann Nestorowicz,Yunjian Li,Settara C. Chandrasekharappa,Craig Chinault,Peter van Tuinen,Richard J. Smith,J. Fielding Hejtmancik,M. Alan Permutt	15
6	A 4-Megabase YAC Contig That Spans the Langer-Giedion Syndrome Region on Human Chromosome 8q24.1: Use in Refining the Location of the Trichorhinophalangeal Syndrome and Multiple Exostoses Genes (TRPS1 and EXT1) 1995 ·Genomics ·Jiakai Hou,Julia Parrish,H.‐J. Lüdecke,(unknown),Y. Wang,Wen‐Shan Chen,(unknown),J. Siegel‐Bartelt,Hope Northrup,(unknown),Craig Chinault,Bernhard Horsthemke,M.J. Wagner,Dan E. Wells	39

About Craig Chinault

Craig Chinault is a scholar working on Genetics, Genetics and Molecular Biology, having authored 6 papers that have together received 189 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (94 citations), Sensory Systems (8 citations) and Cognitive Neuroscience (30 citations). Craig Chinault has collaborated with scholars based in United States, Canada and Sweden. Frequent co-authors include Ankita Patel, Sarika U. Peters, Marwan Shinawi, Trilochan Sahoo, Cindy Skinner, Steven A. Skinner, Bruno Maranda, Arthur L. Beaudet, Roger E. Stevenson and Sau Wai Cheung. Their work appears in journals such as Genome Research, Genomics and European 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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