World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
47
Citations
7423
World Ranking
4130
National Ranking
1781

Overview

A. Craig Chinault is affiliated with Baylor College of Medicine in the United States. Their academic work is connected to this institution, contributing to the scientific community through research activities based at this center.

The available data does not list any recent publications by this researcher, nor does it specify frequent co-authors or commonly targeted publication venues. Information on main and subfields of study or particular topics of work is also not provided, making it difficult to define precise areas of expertise or research focus.

There are no documented book publications or awards associated with A. Craig Chinault in the provided information. Additionally, there is no record of the scientist being deceased, so the profile reflects current status.

The absence of detailed data on research topics, publications, or collaborations suggests that either the public record is limited or that the researcher maintains a low profile in publicly available research databases. However, affiliation with a notable institution such as Baylor College of Medicine indicates involvement in scientific research and higher education.

Best Publications

  • Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes

    Barbara A. Boggs;Peter Cheung;Edith Heard;Edith Heard;David L. Spector

  • Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit.

    Liu Pentao;Carol A. Wise;A. Craig Chinault;Pragna I. Patel

  • Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

    K.-S. Chen;P. Manian;T. Koeuth;L. Potocki

  • Hypoxanthine-guanine phosphoribosyltransferase genes of mouse and Chinese hamster: construction and sequence analysis of cDNA recombinants.

    David S. Konecki;John Brennand;James C. Fuscoe;C.Thomas Caskey;C.Thomas Caskey

  • Development and validation of a CGH microarray for clinical cytogenetic diagnosis

    Sau W Cheung;Chad A Shaw;Wei Yu;Jiangzham Li

  • Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases

    Xinyan Lu;Chad A. Shaw;Ankita Patel;Jiangzhen Li

  • 22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome

    Shay Ben-Shachar;Zhishuo Ou;Chad A. Shaw;John W. Belmont

  • Microarray‐based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

    Sau W. Cheung;Chad A. Shaw;Daryl A. Scott;Ankita Patel

  • Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients.

    Thomas P. Yang;Thomas P. Yang;Pragna I. Patel;Pragna I. Patel;A. Craig Chinault;A. Craig Chinault;John T. Stout

  • Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.

    Zhishuo Ou;Jonathan S Berg;Hagith Yonath;Victoria B Enciso

  • Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.

    Trilochan Sahoo;Sau Wai Cheung;Patricia Ward;Sandra Darilek

  • Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis

    Xin Yan Lu;Mai T. Phung;Chad A. Shaw;Kim Pham

  • Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases

    Lina Shao;Chad A. Shaw;Xin Yan Lu;Trilochan Sahoo

  • Microdeletions including YWHAE in the Miller–Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment

    S C Sreenath Nagamani;F Zhang;O A Shchelochkov;W Bi

  • Organization of the HPRT gene and related sequences in the human genome

    Pragna I. Patel;Robert L. Nussbaum;Paul E. Framson;David H. Ledbetter

  • Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses

    Zhishuo Ou;Sung-Hae L Kang;Chad A Shaw;Condie E Carmack

  • Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

    Patricia B.S. Celestino-Soper;Chad A. Shaw;Stephan J. Sanders;Jian Li

  • Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.

    Daniela del Gaudio;Yaping Yang;Barbara A. Boggs;Eric S. Schmitt

  • Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes

    Zhishuo Ou;Paweł Stankiewicz;Zhilian Xia;Amy M. Breman

  • Microduplications of 22q11.2 are frequently inherited and are associated with variable

    Jonathan S. Berg;Hagith Yonath;Victoria B. Enciso;David T. Miller

Frequent Co-Authors

James R. Lupski
James R. Lupski Baylor College of Medicine
Chad A. Shaw
Chad A. Shaw Baylor College of Medicine
Sau Wai Cheung
Sau Wai Cheung Baylor College of Medicine
Ankita Patel
Ankita Patel Baylor College of Medicine
Arthur L. Beaudet
Arthur L. Beaudet Baylor College of Medicine
Pawel Stankiewicz
Pawel Stankiewicz Baylor College of Medicine
Trilochan Sahoo
Trilochan Sahoo Baylor College of Medicine
Seema R. Lalani
Seema R. Lalani Baylor College of Medicine
Pragna Patel
Pragna Patel Centers for Disease Control and Prevention
Carlos A. Bacino
Carlos A. Bacino Baylor College of Medicine

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Best Scientists Citing A. Craig Chinault