Works matching AU Cody, Jannine D.

Results: 27

Causes of death in individuals with trisomy 18 after the first year of life.

Published in:

American Journal of Medical Genetics. Part A, 2024, v. 194, n. 2, p. 279, doi. 10.1002/ajmg.a.63436

By:

Mehl, Justin M.;
Gelfond, Jonathan;
Carey, John C.;
Cody, Jannine D.

Publication type:

Article

An Evaluation Tool for Collaborative Clinical Research Centers.

Published in:

CTS: Clinical & Translational Science, 2013, v. 6, n. 3, p. 244, doi. 10.1111/cts.12037

By:

Tragus, Robin;
Cody, Jannine D.

Publication type:

Article

Large Inverted Duplications in the Human Genome Form via a Fold-Back Mechanism.

Published in:

PLoS Genetics, 2014, v. 10, n. 1, p. 1, doi. 10.1371/journal.pgen.1004139

By:

Hermetz, Karen E.;
Newman, Scott;
Conneely, Karen N.;
Martin, Christa L.;
Ballif, Blake C.;
Shaffer, Lisa G.;
Cody, Jannine D.;
Rudd, M. Katharine

Publication type:

Article

Mood disorders in individuals with distal 18q deletions.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 879, doi. 10.1002/ajmg.b.32197

By:

Daviss, William B.;
O'Donnell, Louise;
Soileau, Bridgette T.;
Heard, Patricia;
Carter, Erika;
Pliszka, Steven R.;
Gelfond, Jonathan A. L.;
Hale, Daniel E.;
Cody, Jannine D.

Publication type:

Article

Three Novel Mutations in SQSTM1 Identified in Familial Paget's Disease of Bone.

Published in:

Journal of Bone & Mineral Research, 2003, v. 18, n. 10, p. 1748, doi. 10.1359/jbmr.2003.18.10.1748

By:

Johnson-Pais, Teresa L;
Wisdom, Julie H;
Weldon, Korri S;
Cody, Jannine D;
Hansen, Marc F;
Singer, Frederick R;
Leach, Robin J

Publication type:

Article

Variable disease severity associated with a paget's disease predisposition gene.

Published in:

Journal of Bone & Mineral Research, 1999, v. 14, n. S2, p. 17, doi. 10.1002/jbmr.5650140205

By:

Leach, Robin J.;
Singer, Frederick R.;
Cody, Jannine D.;
Roodman, G. David

Publication type:

Article

The Spectrum of Thyroid Abnormalities in Individuals with 18q Deletions.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 4, p. 2259, doi. 10.1210/jc.2004-1630

By:

Schaub, Rebecca L.;
Hale, Daniel E.;
Rose, Susan R.;
Leach, Robin J.;
Cody, Jannine D.

Publication type:

Article

The Spectrum of Growth Abnormalities in Children with 18q Deletions.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 12, p. 4450, doi. 10.1210/jcem.85.12.7016

By:

HALE, DANIEL E.;
CODY, JANNINE D.;
BAILLARGEON, JACQUES;
SCHAUB, REBECCA;
DANNEY, MARK M.;
LEACH, ROBIN J.

Publication type:

Article

Mapping structural differences of the corpus callosum in individuals with 18q deletions using targetless regional spatial normalization.

Published in:

Human Brain Mapping, 2005, v. 24, n. 4, p. 325, doi. 10.1002/hbm.20090

By:

Kochunov, Peter;
Lancaster, Jack;
Hardies, Jean;
Thompson, Paul M.;
Woods, Roger P.;
Cody, Jannine D.;
Hale, Daniel E.;
Laird, Angela;
Fox, Peter T.

Publication type:

Article

Cognitive ability predicts degree of genetic abnormality in participants with 18q deletions.

Published in:

Journal of the International Neuropsychological Society, 2005, v. 11, n. 5, p. 584, doi. 10.1017/s1355617705050691

By:

MARGARET SEMRUD-CLIKEMAN;
NORA M. THOMPSON;
BECKY L. SCHAUB;
ROBIN LEACH;
ANDREA HESTER;
DANIEL E. HALE;
AND JANNINE D. CODY

Publication type:

Article

Understanding type and quality of relationships between individuals with chromosome 18 syndromes and their siblings.

Published in:

Journal of Genetic Counseling, 2024, v. 33, n. 5, p. 1070, doi. 10.1002/jgc4.1823

By:

Larson, Catherine Cody;
O'Donnell, Louise;
Soileau, Bridgette;
Van Riper, Marcia;
Stark, Debra;
Hale, Daniel E.;
Cody, Jannine D.

Publication type:

Article

Otologic characteristics of individuals with deletions of distal 18q.

Published in:

Laryngoscope, 2014, v. 124, n. 11, p. 2606, doi. 10.1002/lary.24769

By:

Perry, Brian P.;
Cody, Jannine D.

Publication type:

Article

Differential expression analysis with global network adjustment.

Published in:

BMC Bioinformatics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2105-14-258

By:

Gelfond, Jonathan A.;
Ibrahim, Joseph G.;
Gupta, Mayetri;
Ming-Hui Chen;
Cody, Jannine D.

Publication type:

Article

Dental caries history in nine children with chromosome 18p deletion syndrome.

Published in:

2000

By:

Hermesch, Charles B.;
Cody, John T.;
Cody, Jannine D.;
Hermesch, C B;
Cody, J T;
Cody, J D

Publication type:

journal article

Chromosome 18 gene dosage map 2.0.

Published in:

Human Genetics, 2018, v. 137, n. 11/12, p. 961, doi. 10.1007/s00439-018-1960-6

By:

Cody, Jannine D.;
Heard, Patricia;
Rupert, David;
Hasi-Zogaj, Minire;
Hill, Annice;
Sebold, Courtney;
Hale, Daniel E.

Publication type:

Article

Genetic determinants of autism in individuals with deletions of 18q.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 155, doi. 10.1007/s00439-010-0839-y

By:

O'Donnell, Louise;
Soileau, Bridgette;
Heard, Patricia;
Carter, Erika;
Sebold, Courtney;
Gelfond, Jon;
Hale, Daniel E.;
Cody, Jannine D.

Publication type:

Article

Abnormal bone mineral content and density in people with tetrasomy 18p.

Published in:

American Journal of Medical Genetics. Part A, 2019, v. 179, n. 3, p. 417, doi. 10.1002/ajmg.a.61005

By:

Moreira, Alvaro;
Das, Hrishikesh;
Hasi‐Zogaj, Minire;
Soileau, Bridgette;
Hill, Annice;
Bruder, Jan M.;
Hale, Daniel E.;
Cody, Jannine D.

Publication type:

Article

Tetrasomy 18p: Report of cognitive and behavioral characteristics.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 7, p. 1474, doi. 10.1002/ajmg.a.37036

By:

O'Donnell, Louise;
Soileau, Bridgette T.;
Sebold, Courtney;
Gelfond, Jonathan;
Hale, Daniel E.;
Cody, Jannine D.

Publication type:

Article

Whole arm deletions of 18p: Medical and developmental effects.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 2, p. 313, doi. 10.1002/ajmg.a.36880

By:

Sebold, Courtney;
Soileau, Bridgette;
Heard, Patricia;
Carter, Erika;
O'Donnell, Louise;
Hale, Daniel E.;
Cody, Jannine D.

Publication type:

Article

Ring 18 molecular assessment and clinical consequences.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 1, p. 54, doi. 10.1002/ajmg.a.36822

By:

Carter, Erika;
Heard, Patricia;
Hasi, Minire;
Soileau, Bridgette;
Sebold, Courtney;
Hale, Daniel E.;
Cody, Jannine D.

Publication type:

Article

Linking chromosome abnormality and copy number variation.

Published in:

2011

By:

Cody, Jannine D.;
Hale, Daniel E.

Publication type:

Editorial

A review of 18p deletions.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2015, v. 169C, n. 3, p. 251, doi. 10.1002/ajmg.c.31445

By:

Hasi‐Zogaj, Minire;
Sebold, Courtney;
Heard, Patricia;
Carter, Erika;
Soileau, Bridgette;
Hill, Annice;
Rupert, David;
Perry, Brian;
Atkinson, Sidney;
O'Donnell, Louise;
Gelfond, Jon;
Lancaster, Jack;
Fox, Peter T.;
Hale, Daniel E.;
Cody, Jannine D.

Publication type:

Article

Consequences of chromsome18q deletions.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2015, v. 169C, n. 3, p. 265, doi. 10.1002/ajmg.c.31446

By:

Cody, Jannine D.;
Sebold, Courtney;
Heard, Patricia;
Carter, Erika;
Soileau, Bridgette;
Hasi‐Zogaj, Minire;
Hill, Annice;
Rupert, David;
Perry, Brian;
O'Donnell, Louise;
Gelfond, Jon;
Lancaster, Jack;
Fox, Peter T.;
Hale, Daniel E.

Publication type:

Article

Identification of Two Novel Chromosome Regions Associated with Isolated Growth Hormone Deficiency.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2010, v. 23, n. 11, p. 1159, doi. 10.1515/jpem.2010.181

By:

Cody, Jannine D.;
Heard, Patricia;
Hale, Daniel

Publication type:

Article

Hemizygosity for SMCHD1 in Facioscapulohumeral Muscular Dystrophy Type 2: Consequences for 18p Deletion Syndrome.

Published in:

Human Mutation, 2015, v. 36, n. 7, p. 679, doi. 10.1002/humu.22792

By:

Lemmers, Richard J. L. F.;
Boogaard, Marlinde L.;
Vliet, Patrick J.;
Donlin‐Smith, Colleen M.;
Nations, Sharon P.;
Ruivenkamp, Claudia A. L.;
Heard, Patricia;
Bakker, Bert;
Tapscott, Stephen;
Cody, Jannine D.;
Tawil, Rabi;
Maarel, Silvère M.

Publication type:

Article

The Chromosome 18 Clinical Resource Center.

Published in:

Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 3, p. 416, doi. 10.1002/mgg3.385

By:

Cody, Jannine D.;
Hasi-Zogaj, Minire;
Heard, Patricia;
Hill, Annice;
Rupert, David;
Sebold, Courtney;
Soileau, Bridgette;
Hale, Daniel E.

Publication type:

Article

Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements.

Published in:

Human Molecular Genetics, 2011, v. 20, n. 19, p. 3769, doi. 10.1093/hmg/ddr293

By:

Luo, Yue;
Hermetz, Karen E.;
Jackson, Jodi M.;
Mulle, Jennifer G.;
Dodd, Anne;
Tsuchiya, Karen D.;
Ballif, Blake C.;
Shaffer, Lisa G.;
Cody, Jannine D.;
Ledbetter, David H.;
Martin, Christa L.;
Rudd, M. Katharine

Publication type:

Article