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1

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, Carlos A. Bacino, Seema R. Lalani, Pawel Stankiewicz, Svetlana A. Yatsenko, Yinfeng Li, Sarah Neill, Amber N. Pursley, A. Craig Chinault, Ankita P

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 155 KB

english, 2008

2

Application of metaphase HR-CGH and targeted chromosomal microarray analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features

B. Nowakowska, P. Stankiewicz, E. Obersztyn, Z. Ou, J. Li, A.C. Chinault, M. Smyk, K. Borg, T. Mazurczak, S.W. Cheung, E. Bocian

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 157 KB

english, 2008

3

11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity

Marwan Shinawi, Trilochan Sahoo, Bruno Maranda, S.A. Skinner, Cindy Skinner, Craig Chinault, Roxanne Zascavage, Sarika U. Peters, Ankita Patel, Roger E. Stevenson, Arthur L. Beaudet

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 943 KB

english, 2011

4

Analysis of DNA Replication by Fluorescencein SituHybridization

Barbara A. Boggs, A.Craig Chinault

Journal:

Year:

1997

Language:

english

File:

PDF, 1.40 MB

english, 1997

5

15. Application of oligonucleotide aCGH to the diagnosis of mitochondrial DNA deletion and depletion syndromes

A. Craig Chinault, Chad Shaw, Lin-Ya Tang, Lee-Jun C. Wong

Journal:

Year:

2009

Language:

english

File:

PDF, 50 KB

english, 2009

6

Comprehensive analysis of entire mitochondrial genome by long-range PCR and next generation sequencing for the diagnosis of mitochondrial disorders: Yield of 216 cases

Renkui Bai, Jaimie Higgs, Sharon Suchy, Mustafa Saifi, Melanie Knight, Sabrina Buchholz, Sonia Benhamed, Dolores Arjona, Barbara Boggs, Craig Chinault, Yuriy Shevchenko, Nizar Smaoui, Gabriele Richard

Journal:

Year:

2012

Language:

english

File:

PDF, 64 KB

english, 2012

7

PCR-based target sequence enrichment and next generation sequencing of 24 nuclear genes for the diagnosis of mitochondrial disorders: Yield of 262 cases

Renkui Bai, Jaimie Higgs, Sharon Suchy, Mustafa Saifi, Melanie Knight, Federica Gibellini, Sabrina Buchholz, Sonia Benhamed, Dolores Arjona, Barbara Boggs, Craig Chinault, Yuriy Shevchenko, Nizar Smao

Journal:

Year:

2012

Language:

english

File:

PDF, 81 KB

english, 2012

8

PCR-based targeted enrichment and next-generation sequencing of 101 nuclear genes for the diagnosis of mitochondrial disorders

Renkui Bai, Jaimie Higgs, Sharon Suchy, Federica Gibellini, Melanie Knight, Sabrina Buchholz, Sonia Benhamed, Dolores Arjona, Craig Chinault, Rhonda Brandon, Nizar Smaoui, Gabriele Richard, Sherri Bal

Journal:

Year:

2012

Language:

english

File:

PDF, 59 KB

english, 2012

9

Dosimetric Comparison of VMAT-Based Lung SBRT Treatments With and Without a Flattening Filter: An Interinstitutional Study

Maidment, B.W., Geesey, C., Xie, C., Chinault, J., Best, R., Larner, J.M., Wijesooriya, K.

Journal:

International Journal of Radiation Oncology*Biology*Physics

Year:

2014

Language:

english

File:

PDF, 55 KB

english, 2014

10

Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia

Ankita Patel, Sung-Hae Kang, Patrick Alan Lennon, Yin Feng Li, P. Nagesh Rao, Lynne Abruzzo, Chad Shaw, Alan Craig Chinault, Sau W Cheung

Journal:

American Journal of Hematology

Year:

2008

Language:

english

File:

PDF, 293 KB

english, 2008

11

Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome

Kimberly A. Ellison, E. Jill Roth, Edward R. B. McCabe, A. Craig Chinault, Huda Y. Zoghbi

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 1.07 MB

english, 1993

12

Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation

Frank J. Probst, Elizabeth R. Roeder, Victoria B. Enciso, Zhishuo Ou, M. Lance Cooper, Patricia Eng, Jiangzhen Li, Yanghong Gu, Robert F. Stratton, A. Craig Chinault, Chad A. Shaw, V. Reid Sutton, Sau

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 257 KB

english, 2007

13

Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome

Oleg A. Shchelochkov, Ankita Patel, George M. Weissenberger, A. Craig Chinault, Joanna Wiszniewska, Priscilla H. Fernandes, Christine Eng, Mary K. Kukolich, V. Reid Sutton

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 199 KB

english, 2008

14

Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement

Zhishuo Ou, Donna M. Martin, Jirair K. Bedoyan, M. Lance Cooper, A. Craig Chinault, Pawel Stankiewicz, Sau W. Cheung

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 382 KB

english, 2008

15

A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies

Daniel R. Jensen, Donna M. Martin, Stephen Gebarski, Trilochan Sahoo, Ellen K. Brundage, A. Craig Chinault, Edgar A. Otto, Moumita Chaki, Friedhelm Hildebrandt, Sau Wai Cheung, Marci M. Lesperance

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 281 KB

english, 2009

16

Mosaic deletion 11p13 in a child with dopamine beta-hydroxylase deficiency—Case report and review of the literature

A. Erez, J. Li, M.T. Geraghty, S. Ben-Shachar, M.L. Cooper, D.E. Mensing, K.D. Vonalt, Z. Ou, A.N. Pursley, A.C. Chinault, A. Patel, S.W. Cheung, T. Sahoo

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 351 KB

english, 2010

17

Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) results

Sung-Hae L. Kang, Chad Shaw, Zhishuo Ou, Patricia A. Eng, M. Lance Cooper, Amber N. Pursley, Trilochan Sahoo, Carlos A. Bacino, A. Craig Chinault, Pawel Stankiewicz, Ankita Patel, James R. Lupski, Sau

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 730 KB

english, 2010

18

Characterization of the deletion breakpoints in a patient with steroid sulfatase deficiency

Pauline H. Yen, Giovanni B. Ferrero, A. Craig Chinault, Thuluvancheri Mohandas, Andrea Ballabio

Journal:

Year:

1994

Language:

english

File:

PDF, 207 KB

english, 1994

19

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, Jennifer A. Lee, Trilochan Sahoo, Hoang T. Pham, Joanna Wiszniewska, A. Craig Chinault, Arthur L. Beaudet, Christine M. Eng

Journal:

Year:

2008

Language:

english

File:

PDF, 389 KB

english, 2008

20

Ultrastructural and biochemical comparisons of nuclear matrices prepared by high salt or LIS extraction

Harold C. Smith, Robert L. Ochs, Dong Lin, A. Craig Chinault

Journal:

Molecular and Cellular Biochemistry

Year:

1987

Language:

english

File:

PDF, 1.03 MB

english, 1987

21

Yeast ARS function and nuclear matrix association coincide in a short sequence from the humanHPRTlocus

Robert C. Sykes, Dong Lin, Sung J. Hwang, Paul E. Framson, A. Craig Chinault

Journal:

Molecular Genetics and Genomics

Year:

1988

Language:

english

File:

PDF, 1.00 MB

english, 1988

22

Reduced levels of histone H3 acetylation on the inactive X chromosome in human females

Barbara A. Boggs, Bernadette Connors, Richard E. Sobel, A. Craig Chinault, C. David Allis

Journal:

Year:

1996

Language:

english

File:

PDF, 675 KB

english, 1996

23

Replication timing properties, of the humanHPRTlocus on active, inactive and reactivated X chromosomes

Prem S. Subramanian, A. Craig Chinault

Journal:

Somatic Cell and Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 1.25 MB

english, 1997

24

Replication timing properties across the pseudoautosomal region boundary and cytogenetic band boundaries on human distal Xp

Kristin Bilyeu, A. Craig Chinault

Journal:

Year:

1998

Language:

english

File:

PDF, 695 KB

english, 1998

25

Immunofluorescent studies of human chromosomes with antibodies against phosphorylated H1 histone

Barbara A. Boggs, C. David Allis, A. Craig Chinault

Journal:

Year:

2000

Language:

english

File:

PDF, 202 KB

english, 2000

26

Physical mapping and genomic structure of the Lowe syndrome gene OCRL1

R. L. Nussbaum, Bonnie M. Orrison, Pasi A. Jänne, Lawrence Charnas, A. Craig Chinault

Journal:

Year:

1997

Language:

english

File:

PDF, 76 KB

english, 1997

27

Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization

N Brunetti-Pierri, DK Grange, Z Ou, DA Peiffer, SKG Peacock, ML Cooper, PA Eng, SR Lalani, AC Chinault, KL Gunderson, WJ Craigen, S-W Cheung

Journal:

Clinical Genetics

Year:

2007

Language:

english

File:

PDF, 612 KB

english, 2007

28

Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome

S-HL Kang, A Scheffer, Z Ou, J Li, F Scaglia, J Belmont, SR Lalani, E Roeder, V Enciso, S Braddock, J Buchholz, S Vacha, AC Chinault, SW Cheung, CA Bacino

Journal:

Clinical Genetics

Year:

2007

Language:

english

File:

PDF, 606 KB

english, 2007

29

Identification of critical regions for clinical features of distal 10q deletion syndrome

SA Yatsenko, MC Kruer, PI Bader, D Corzo, J Schuette, CE Keegan, B Nowakowska, S Peacock, WW Cai, DA Peiffer, KL Gunderson, Z Ou, AC Chinault, SW Cheung

Journal:

Clinical Genetics

Year:

2009

Language:

english

File:

PDF, 630 KB

english, 2009

30

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

Hildebrand, Beth M., Caskey, C. Thomas, Yang, Thomas P., Patel, Pragna I., Chinault, A. Craig, Stout, John T., Jackson, Laird G.

Journal:

Year:

1984

File:

PDF, 387 KB

1984

31

Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss

Nagamani, Sandesh Chakravarthy Sreenath, Erez, Ayelet, Eng, Christine, Ou, Zhishuo, Chinault, Craig, Workman, Laura, Coldwell, James, Stankiewicz, Pawel, Patel, Ankita, Lupski, James R

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 298 KB

english, 2008

32

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

Chen, Ken-Shiung, Manian, Prasad, Koeuth, Thearith, Potocki, Lorraine, Zhao, Qi, Chinault, A. Craig, Lee, Cheng Chi, Lupski, James R.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 1.29 MB

1997

33

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

Boggs, Barbara A., Cheung, Peter, Heard, Edith, Spector, David L., Chinault, A. Craig, Allis, C. David

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 534 KB

english, 2001

34

Functional identification of LZTS1 as a candidate prostate tumor suppressor gene on human chromosome 8p22

Cabeza-Arvelaiz, Yofre, Sepulveda, Jorge L, Lebovitz, Russell M, Thompson, Timothy C, Chinault, A Craig

Journal:

Year:

2001

Language:

english

File:

PDF, 622 KB

english, 2001

35

LAPSER1: a novel candidate tumor suppressor gene from 10q24.3

Cabeza-Arvelaiz, Yofre, Thompson, Timothy C, Sepulveda, Jorge L, Chinault, A Craig

Journal:

Year:

2001

Language:

english

File:

PDF, 590 KB

english, 2001

36

Comparative study of DNase I sensitivity at the X-linked humanHPRTlocus

Dong Lin, A. Craig Chinault

Journal:

Somatic Cell and Molecular Genetics

Year:

1988

Language:

english

File:

PDF, 1.36 MB

english, 1988

37

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

Pragna I. Patel, Robert L. Nussbaum, Paul E. Framson, David H. Ledbetter, C. Thomas Caskey, A. Craig Chinault

Journal:

Somatic Cell and Molecular Genetics

Year:

1984

Language:

english

File:

PDF, 967 KB

english, 1984

38

Physical and transcription map of double minutes with micro-dissected DNA from a human breast cancer cell line

S. Sen, H. Zhou, P. Sen, A.C. Chinault

Journal:

Cancer Genetics and Cytogenetics

Year:

1995

Language:

english

File:

PDF, 158 KB

english, 1995

39

Characterization of human genomic yeast artificial chromosome inserts containing hexokinase 1 coding information on chromosome 10

Bruce D. Gelb, Kim C. Worley, Lisa D. Griffin, Volker Admas, A.Craig Chinault, Edward R.B. McCabe

Journal:

Biochemical Medicine and Metabolic Biology

Year:

1992

Language:

english

File:

PDF, 382 KB

english, 1992

40

601: Rapid prenatal diagnosis of cytogenetic abnormalities by array CGH analysis

Sau Wai Cheung, Chad Shaw, Sung-Hae Kang, Marcia Simovich, Amber Pursley, Sandra Darilek, Patricia Ward, A. Craig Chinault, Ankita Patel, James Lupski, Arthur Beaudet, Christine Eng, Ignatia van den V

Journal:

American Journal of Obstetrics and Gynecology

Year:

2007

Language:

english

File:

PDF, 47 KB

english, 2007

41

Yeast Artificial Chromosome Cloning in the Glycerol Kinase and Adrenal Hypoplasia Congenita Region of Xp21

K.C. Worley, K.A. Ellison, Y-H. Zhang, D-F. Wang, J. Mason, E.J. Roth, V. Adams, D.D. Fogt, X.M. Zhu, J.A. Towbin, A.C. Chinault, H. Zoghbi, E.R.B. McCabe

Journal:

Year:

1993

File:

PDF, 636 KB

1993

42

A Yeast Artificial Chromosome Contig Linking the Steroid Sulfatase and Kallmann Syndrome Loci on the Human X Chromosome Short Arm

Wen-Chuan Lee, Giovanni B. Ferrero, A.Craig Chinault, Pauline H. Yen, Andrea Ballabio

Journal:

Year:

1993

File:

PDF, 433 KB

1993

43

Isolation and Chromosomal Mapping of Genomic Clones Encoding the Human Fatty Acid Synthase Gene

Arumugam Jayakumar, Subrahmanyam S. Chirala, A.Craig Chinault, Antonio Baldini, Lutfi Abu-Elheiga, Salih J. Wakil

Journal:

Year:

1994

File:

PDF, 399 KB

1994

44

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)

J. Hou, J. Parrish, H.-J. Lüdecke, M. Sapru, Y. Wang, W. Chen, A. Hill, J. Siegel-Bartelt, H. Northrup, F.F.B. Elder, C. Chinault, B. Horsthemke, M.J. Wagner, D.E. Wells

Journal:

Year:

1995

File:

PDF, 840 KB

1995

45

A 2.8-Mb Clone Contig of the Multiple Endocrine Neoplasia Type 1 (MEN1) Region at 11q13

Siradanahalli C. Guru, Shodimu-Emmanuel Olufemi, Pachiappan Manickam, Christiano Cummings, Linn M. Gieser, Brian L. Pike, Michael L. Bittner, Yuan Jiang, A.Craig Chinault, Norma J. Nowak, Anna Brzozow

Journal:

Year:

1997

Language:

english

File:

PDF, 633 KB

english, 1997

46

BAC Contig from a 3-cM Region of Mouse Chromosome 11 Surrounding Brca1

Mark Pershouse, Jiewen Li, Chun Yang, Hong Su, Ellen Brundage, Weimei Di, Patrick J. Biggs, Allan Bradley, A.Craig Chinault

Journal:

Year:

2000

Language:

english

File:

PDF, 79 KB

english, 2000

47

High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)

Irène Wang, Brunella Franco, Giovanni B. Ferrero, A.Craig Chinault, Jean Weissenbach, Ilya Chumakov, Denis Le Paslier, Jacqueline Levilliers, Albrecht Klink, Gudrun A. Rappold, Andrea Ballabio, Christ

Journal:

Year:

1995

Language:

english

File:

PDF, 1014 KB

english, 1995

48

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, Millan S. Patel, Marybeth Hummel, Stephen Amato, Nicole Tartaglia, Jonathan Berg, V. Reid Sutton, Seema R. Lalani, A. Craig Chinault, Sau W

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 589 KB

english, 2008

49

Respiratory Uncoupling in Skeletal Muscle Delays Death and Diminishes Age-Related Disease

Allison C. Gates, Carlos Bernal-Mizrachi, Sharon L. Chinault, Chu Feng, Jochen G. Schneider, Trey Coleman, James P. Malone, R. Reid Townsend, Manu V. Chakravarthy, Clay F. Semenkovich

Journal:

Cell Metabolism

Year:

2007

Language:

english

File:

PDF, 1.24 MB

english, 2007

50

Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb

S. Banfi, M.-Y. Chung, T.J. Kwiatkowski Jr., L.P.W. Ranum, A.E. McCall, A.C. Chinault, H.T. Orr, H.Y. Zoghbi

Journal:

Year:

1993

Language:

english

File:

PDF, 1.27 MB

english, 1993