C. Morton

C. Cremers, C. Morton, H. Kremer, 2005, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder

C. Morton, A. Griffith, T. Makishima, 2005, Human Genetics.

Uterine leiomyomata with deletions of Ip represent a distinct cytogenetic subgroup associated with unusual histologic features

P. Cin, C. Morton, B. Quade, 2006, Genes, chromosomes & cancer.

Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders

Erez Lieberman Aiden, Ryan L. Collins, S. G. Temel, 2022, medRxiv.

Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin

C. Morton, M. Talkowski, D. Harris, 2018, European Journal of Human Genetics.

Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements.

Fowzan S Alkuraya, Michael E Talkowski, Karen W Gripp, 2017, American journal of human genetics.

Cytogenetic evidence of clonality in a case of pigmented villonodular synovitis

J. Fletcher, C. Morton, J. Corson, 1991, Cancer.

Gene therapy for hearing loss.

C. Morton, Richard J. H. Smith, S. B. Shibata, 2019, Human molecular genetics.

Trisomy 5 and trisomy 7 are nonrandom aberrations in pigmented villonodular synovitis: Confirmation of trisomy 7 in uncultured cells

J. Fletcher, C. Morton, A. Rosenberg, 1992, Genes, chromosomes & cancer.

Comprehensive clinically oriented workflow for nucleotide level resolution and interpretation in prenatal diagnosis of de novo apparently balanced chromosomal translocations in their genomic landscape

C. Morton, Joana Fino, D. David, 2020, Human Genetics.

Functional Analysis of SPECC1L in Craniofacial Development and Oblique Facial Cleft Pathogenesis

C. Morton, R. Maas, P. Pietschmann, 2014, Plastic and reconstructive surgery.

Newborn hearing screening--a silent revolution.

C. Morton, W. Nance, 2006, The New England journal of medicine.

Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells.

P. Leder, C. Morton, G. Lenoir, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Hodgkin's disease, lymphomatoid papulosis, and cutaneous T-cell lymphoma derived from a common T-cell clone.

C. Morton, S. Balk, M. Kadin, 1992, The New England journal of medicine.

Human vitamin C (L-ascorbic acid) transporter SVCT1.

S. Weremowicz, M. Hediger, C. Morton, 2000, Biochemical and biophysical research communications.

Quinacrine mustard and nucleolar organizer region heteromorphisms in twins.

C. Morton, W. Nance, L. Corey, 1981, Acta geneticae medicae et gemellologiae.

Historical and Clinical Perspectives on Chromosomal Translocations.

C. Morton, E. Wilch, 2018, Advances in experimental medicine and biology.

Stain intensity of human nucleolus organizer region reflects incorporation of uridine into mature ribosomal RNA.

C. Morton, W. Nance, B. Wolf, 1983, Experimental Cell Research.

Expression studies of osteoglycin/mimecan (OGN) in the cochlea and auditory phenotype of Ogn-deficient mice

E. Tasheva, G. Conrad, C. Morton, 2008, Hearing Research.

Pleiotropic defects in ataxia-telangiectasia protein-deficient mice.

P. Leder, C. Morton, A. Elson, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21.

L. Holmes, C. Lee, C. Morton, 2001, American journal of medical genetics.

Clonal 6p21 rearrangement is restricted to the mesenchymal component of an endometrial polyp

G. Pinkus, J. Fletcher, C. Morton, 1992, Genes, chromosomes & cancer.

Consistent cytogenetic aberrations in hepatoblastoma: A common pathway of genetic alterations in embryonal liver and skeletal muscle malignancies?

J. Fletcher, B. Korf, C. Morton, 1991, Genes, chromosomes & cancer.

A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children

C. Morton, S. Amr, Jun Shen, 2019, Genetics in Medicine.

Human immunoglobulin heavy chain genes map to a region of translocations in malignant B lymphocytes.

P. Leder, C. Morton, I. Kirsch, 1982, Science.

Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China

Huanming Yang, Jian Wang, Zhiyu Peng, 2018, bioRxiv.

Characterization of an Abundant COL9A1 Transcript in the Cochlea with a Novel 3′ UTR: Expression Studies and Detection of miRNA Target Sequence

C. Morton, T. A. Sivakumaran, A. Giersch, 2006, Journal of the Association for Research in Otolaryngology.

Using population admixture to help complete maps of the human genome

Alkes L. Price, Heng Li, Bogdan Pasaniuc, 2013, Nature Genetics.

Tumor-Associated Endothelial Cells with Cytogenetic Abnormalities

Dhara N. Amin, C. Morton, M. Klagsbrun, 2004, Cancer Research.

Disruption of neurexin 1 associated with autism spectrum disorder.

Yiping Shen, Ilse Noens, Mark J Daly, 2008, American journal of human genetics.

Genome-wide association analysis identifies 27 novel loci associated with uterine leiomyomata revealing common genetic origins with endometriosis

J. Cook, A. Morris, R. Cantor, 2018, bioRxiv.

Expression profiling of uterine leiomyomata cytogenetic subgroups reveals distinct signatures in matched myometrium: transcriptional profilingof the t(12;14) and evidence in support of predisposing genetic heterogeneity.

Tae-Min Kim, Peter J Park, Elizabeth A Stewart, 2012, Human molecular genetics.

Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma

P. Cin, C. Morton, B. Quade, 2010, Genes, chromosomes & cancer.

Constitutional rearrangement of the architectural factor HMGA2: a novel human phenotype including overgrowth and lipomas.

Cynthia C Morton, C. Morton, A. Ligon, 2005, American journal of human genetics.

Expression of HMGIY in three uterine leiomyomata with complex rearrangements of chromosome 6.

S. Weremowicz, C. Morton, A. Ligon, 1999, Cancer genetics and cytogenetics.

Chromosome Translocation

C. Morton, E. Wilch, Yu Zhang, 2018, Advances in Experimental Medicine and Biology.

Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus.

S. Scherer, J. Rosenfeld, E. Eichler, 2013, American journal of human genetics.

Cytogenetics and Cochlear Expressed Sequence Tags (ESTs) for Identification of Genes Involved in Hearing and Deafness

C. Morton, A. Giersch, 2002 .

A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mapping.

A. Hudspeth, S. Heller, S. Weremowicz, 2000, Genomics.

Diagnostic relevance of clonal cytogenetic aberrations in malignant soft-tissue tumors.

G. Pinkus, J. Fletcher, C. Morton, 1991, The New England journal of medicine.

Isolation from Cochlea of a Novel Human Intronless Gene with Predominant Fetal Expression

Joe C. Adams, O. Ohara, C. Morton, 2004, Journal of the Association for Research in Otolaryngology.

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

H. Rehm, C. Cremers, C. Möller, 1998, Science.

X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4.

C. Morton, Kerry K. Brown, J. MacKenzie, 2014, American journal of audiology.

Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35)

C. Morton, Kerry K. Brown, H. Ferguson, 2009, Human Genetics.

Genetics, genomics and gene discovery in the auditory system.

C. Morton, 2002, Human molecular genetics.

The human phosphoglycerate kinase multigene family. HLA-associated sequences and an X-linked locus containing a processed pseudogene and its functional counterpart.

A. Michelson, S. Orkin, C. Morton, 1985, Journal of Biological Chemistry.

Beginning of a molecular era in hearing and deafness

C. Morton, N. G. Robertson, 1999 .

Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness.

C. Morton, A. J. Yee, Z. Weng, 1999, Human molecular genetics.

Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening.

F. Bieber, C. Morton, N. G. Robertson, 1994, Genomics.

Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies.

L. Shaffer, Cheol‐Hee Kim, M. MacDonald, 2012, American journal of human genetics.

Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis

P. Park, C. Morton, B. Quade, 2009, Genes, chromosomes & cancer.

Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1

M. MacDonald, J. Gusella, C. Morton, 2005, Journal of Medical Genetics.

Uterine Leiomyomata with t(10;17) Disrupt the Histone Acetyltransferase MORF

P. Cin, C. Morton, S. Herrick, 2004, Cancer Research.

Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.

J. Rosenfeld, B. V. van Bon, M. Fichera, 2011, American journal of human genetics.

Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research.

Yiping Shen, Colby Chiang, Michael E Talkowski, 2011, American journal of human genetics.

Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities

J. Gusella, C. Morton, M. Talkowski, 2014, Molecular Psychiatry.

CHAPTER 31 – Cytogenetics in Reproduction

C. Morton, Charles Lee, 2009 .

GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank.

C. Morton, A. Payton, F. Williams, 2019, American journal of human genetics.

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

C. Morton, J. Touchman, T. Friedman, 1998, Science.

Cytogenetic findings in pediatric adipose tumors: Consistent rearrangement of chromosome 8 in lipoblastoma

J. Fletcher, C. Morton, H. Kozakewich, 1993, Genes, chromosomes & cancer.

Leiomyomata: heritability and cytogenetic studies.

C. Morton, A. Ligon, 2001, Human reproduction update.

Analysis of androgen receptor DNA reveals the independent clonal origins of uterine leiomyomata and the secondary nature of cytogenetic aberrations in the development of leiomyomata

J. Sklar, R. Mashal, C. Morton, 1994, Genes, chromosomes & cancer.

Chromosome aberrations in uterine smooth muscle tumors: potential diagnostic relevance of cytogenetic instability.

J. Fletcher, C. Morton, J. Lage, 1990, Cancer research.

Cytogenetic abnormalities in uterine myomas are associated with myoma size.

R. Cantor, R. Barbieri, S. Weremowicz, 1998, Molecular human reproduction.

Chromosomal translocation t(8;12) induces aberrant HMGIC expression in aggressive angiomyxoma of the vulva

S. Weremowicz, C. Morton, B. Quade, 2001, Genes, chromosomes & cancer.

Genetic heterogeneity among uterine leiomyomata: insights into malignant progression.

C. Morton, J. Hodge, Jennelle C. Hodge, 2007, Human molecular genetics.

The del(7q) subgroup in uterine leiomyomata: genetic and biologic characteristics. Further evidence for the secondary nature of cytogenetic abnormalities in the pathobiology of uterine leiomyomata.

C. Morton, Y. Xing, W. Powell, 1997, Cancer genetics and cytogenetics.

HMGI(Y) expression in human uterine leiomyomata. Involvement of another high-mobility group architectural factor in a benign neoplasm.

C. Morton, T. Collins, A. Williams, 1997, The American journal of pathology.

Localization and expression of the human estrogen receptor beta gene in uterine leiomyomata

Simak Ali, S. Weremowicz, C. Morton, 1998, Genes, chromosomes & cancer.

Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomas

R. Kucherlapati, S. Weremowicz, C. Morton, 1996, Genes, chromosomes & cancer.

A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosis

J. Fletcher, S. Weremowicz, C. Morton, 2000, Genes, chromosomes & cancer.

Is Hmgic rearranged due to cryptic paracentric inversion of 12q in karyotypically normal uterine leiomyomas?

C. Morton, Stanislawa Weremowicz, 1999, Genes, chromosomes & cancer.

The genetic heterogeneity of uterine leiomyomata.

C. Morton, P. Somasundaram, Melissa K. Lobel, 2006, Obstetrics and gynecology clinics of North America.

Cytogenetic and other genetic insights into the pathogenesis of uterine leiomyomata

P. Cin, C. Morton, 2005 .

Rearrangements in 12 q 15 Molecular Mechanism in Uterine Leiomyomata with Are not a Common HMGA 2 Fusion Transcripts Involving Updated

C. Ladd, S. Weremowicz, P. Cin, 2003 .

Genetic approaches to the study of uterine leiomyomata.

C. Morton, 2000, Environmental health perspectives.

Translocations in 7q22 define a critical region in uterine leiomyomata.

S. Weremowicz, C. Morton, M. Rein, 1994, Cancer genetics and cytogenetics.

The t(10;14)(q24;q11) of T-cell acute lymphoblastic leukemia juxtaposes the delta T-cell receptor with TCL3, a conserved and activated locus at 10q24.

S. Korsmeyer, L. Deaven, C. Roberts, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Translocations that highlight chromosomal regions of differentiated activity.

S. Korsmeyer, C. Morton, I. Kirsch, 1985, Cancer genetics and cytogenetics.

Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice.

N. Copeland, N. Jenkins, C. Morton, 1997, Human molecular genetics.

Multicolor karyotypic interpretation of a heterochromatin-associated marker chromosome in a dysmorphic girl with developmental delay.

S. Weremowicz, C. Morton, J. Picker, 2002, American journal of medical genetics.

Novel Isoform of Lymphoid Adaptor FYN-T-binding Protein (FYB-130) Interacts with SLP-76 and Up-regulates Interleukin 2 Production*

S. Weremowicz, C. Morton, C. Rudd, 1999, The Journal of Biological Chemistry.

Human γ-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7

T. Waldmann, J. Seidman, T. Shows, 1985, Nature.

Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases †

F. Bieber, S. Weremowicz, C. Morton, 2001, Prenatal diagnosis.

Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and mice.

M. Kelz, K. Ligon, J. Gusella, 2007, American journal of human genetics.

Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1→p14

L. H. Haley, R. Eddy, T. Shows, 2001, Cytogenetic and Genome Research.

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.

S. Schwartz, C. Lee, C. Morton, 2001, Human molecular genetics.

Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele

C. Panhuysen, C. Morton, E. Stewart, 2009, Human Genetics.

Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partner

S. Orkin, N. Andrews, S. Weremowicz, 1993, Molecular and cellular biology.

Identification and function of long non-coding RNA

Carl Ernst, C. Morton, C. Ernst, 2013, Front. Cell. Neurosci..

The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing

C. Morton, K. Choy, A. Giersch, 2022, International journal of neonatal screening.

Ryan L. Collins, J. Gusella, C. Morton, 2016, European Journal of Human Genetics.

Low-pass genome sequencing-based detection of absence of heterozygosity: validation in clinical cytogenetics

C. Morton, K. Choy, T. Leung, 2021, Genetics in Medicine.

Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex.

R Kucherlapati, C J Vaughan, R. Kucherlapati, 2000, The Journal of clinical investigation.

Balanced Chromosomal Rearrangement Detection by Low‐Pass Whole‐Genome Sequencing

Hui Jiang, Fang Chen, Jun Wang, 2018, Current protocols in human genetics.

Identification of Balanced Chromosomal Rearrangements Previously Unknown Among Participants in the 1000 Genomes Project: Implications for Interpretation of Structural Variation in Genomes and the Future of Clinical Cytogenetics

Hui Jiang, Zhenjun Yang, Jianying Yuan, 2017, Genetics in Medicine.

Candidate loci for Zimmermann–Laband syndrome at 3p14.3

M. MacDonald, J. Gusella, C. Morton, 2007, American journal of medical genetics. Part A.

Primary Parauterine Leiomyoma With a t(6;14)

S. Weremowicz, C. Morton, B. Quade, 1999, Genes, chromosomes & cancer.

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis

S. Cheung, C. Morton, K. Choy, 2019, Genetics in Medicine.

Yield of Additional Genetic Testing after Chromosomal Microarray for Diagnosis of Neurodevelopmental Disability and Congenital Anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

S. Schwartz, David T. Miller, C. Morton, 2018, Genetics in Medicine.

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Ryan L. Collins, D. MacArthur, Daisuke Sato, 2017, Nature Genetics.

Genomic alterations in myeloid neoplasms with novel, apparently balanced translocations.

D. Costa, C. Morton, R. Stone, 2011, Cancer genetics.

Impaired nonhomologous end-joining provokes soft tissue sarcomas harboring chromosomal translocations, amplifications, and deletions.

L. Chin, F. Alt, R. DePinho, 2001, Molecular cell.

Resolving Breakpoints of Chromosomal Rearrangements at the Nucleotide Level Using Sanger Sequencing

C. Morton, R. Piña-Aguilar, Katarena Nalbandian, 2020, Current protocols in human genetics.

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.

S. Cheung, Yuan Jiang, Huanming Yang, 2019, American journal of human genetics.

The Iceberg under Water: Unexplored Complexity of Chromoanagenesis in Congenital Disorders.

C. Morton, C. Zepeda-Mendoza, 2019, American journal of human genetics.

3C-PCR: a novel proximity ligation-based approach to phase chromosomal rearrangement breakpoints with distal allelic variants

C. Morton, Samantha L. P. Schilit, 2017, Human Genetics.

Clinical diagnosis by whole-genome sequencing of a prenatal sample.

Michael E Talkowski, Naveed Hussain, Lisa G Shaffer, 2012, The New England journal of medicine.

NFIA Haploinsufficiency Is Associated with a CNS Malformation Syndrome and Urinary Tract Defects

C. Walsh, K. Devriendt, J. Gusella, 2007, PLoS genetics.

Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole‐genome sequencing

V. Jobanputra, C. Morton, M. Talkowski, 2015, Prenatal diagnosis.

Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities.

Yiping Shen, Manolis Kellis, Va Lip, 2012, American journal of human genetics.

A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPs.

P. Leder, R. Eddy, T. Shows, 1991, American journal of human genetics.

Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis†.

J. Gusella, C. Morton, M. Talkowski, 2016, Human molecular genetics.

Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell line

J. Fletcher, C. Morton, S. Diehl, 1992, Human Genetics.

Association of trisomy 8 and squamous differentiation in an endometrial adenocarcinoma.

J. Aster, J. Fletcher, C. Morton, 1989, Cancer genetics and cytogenetics.

1q42∼q44 is rarely cytogenetically involved in sporadic uterine leiomyomata

P. Cin, C. Morton, 2002 .

Epstein-Barr virus exploits intrinsic B-lymphocyte transcription programs to achieve immortal cell growth

John Quackenbush, E. Kieff, E. Johannsen, 2011, Proceedings of the National Academy of Sciences.

Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24)

P. D. Dal Cin, S. Weremowicz, C. Morton, 2003, Genes, chromosomes & cancer.

Genetics of uterine leiomyomata.

C. Morton, A. Ligon, 2000, Genes, chromosomes & cancer.

ORC5L, a New Member of the Human Origin Recognition Complex, Is Deleted in Uterine Leiomyomas and Malignant Myeloid Diseases*

Anindya Dutta, C. Morton, A. Ligon, 1998, The Journal of Biological Chemistry.

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

M. King, Ming K. Lee, C. Morton, 1998, Science.

Lineage-restrict ed Clonality inBiphasic Solid Tumors

G. Pinkus, J. Fletcher, C. Morton, 1991 .

Identification of PKDL, a Novel Polycystic Kidney Disease 2-Like Gene Whose Murine Homologue Is Deleted in Mice with Kidney and Retinal Defects*

S. Weremowicz, C. Morton, W. Ji, 1998, The Journal of Biological Chemistry.

RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS

C L Bradshaw, L. Shaffer, C. Disteche, 1997, Prenatal diagnosis.

Localization of the human angiogenin gene to chromosome band 14q11, proximal to the T cell receptor alpha/delta locus.

S. Weremowicz, C. Morton, E. Fox, 1990, American journal of human genetics.

Spectrum of genes involved in a unique case of Potocki Schaffer syndrome with a large chromosome 11 deletion

Yiping Shen, C. Morton, Hyung-Goo Kim, 2014, Clinical neuropathology.

Section E6.5–6.8 of the ACMG technical standards and guidelines: chromosome studies of lymph node and solid tumor–acquired chromosomal abnormalities

W. Sanger, C. Morton, F. Mikhail, 2016, Genetics in Medicine.

Disruption of ROBO2 Is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux

J. Lupski, C. Wijmenga, S. Kulkarni, 2007 .

Ovarian granulosa-stromal cell tumors are characterized by trisomy 12.

J. Fletcher, C. Morton, Cynthia C. Morton, 1991, The American journal of pathology.

Localization of the beta-globin gene by chromosomal in situ hybridization.

S. Orkin, C. Morton, R. Taub, 1984, American journal of human genetics.

Germline and Rearranged, Duplicated and Dispersed Forms

S. Korsmeyer, C. Morton, W. Graninger, 1988 .

2014 Presidential Address: The time of our lives.

C. Morton, 2015, American journal of human genetics.

Detection and localization of an extra HLA locus in a karyotypically normal male by chromosomal in situ hybridization

G. Evans, C. Morton, I. Kirsch, 1986, Clinical genetics.

Detection of a frequent restriction fragment length polymorphism in the human T cell antigen receptor beta chain locus. A potential diagnostic tool.

J. Seidman, P. Leder, C. Morton, 1985, The Journal of clinical investigation.

Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

S. Schwartz, David T. Miller, C. Martin, 2018, Genetics in Medicine.

Human Chromosome 7: DNA Sequence and Biology

Junjun Zhang, Nazneen Rahman, Alexander K. Hudek, 2003, Science.

MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus

Ronald Berezney, Kasper Lage, Raymond M. Anchan, 2015, Human molecular genetics.

MATR 3 disruption in human and mouse associated with bicuspid aortic valve , aortic coarctation and patent ductus arteriosus

K. Lage, J. Gusella, C. Morton, 2015 .

The cell adhesion gene PVRL3 is associated with congenital ocular defects

J. Gusella, C. Morton, M. Talkowski, 2012, Human Genetics.

NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness

Richard L Robertson, Fowzan S Alkuraya, Cynthia C Morton, 2009, American journal of medical genetics. Part A.

Methylthioadenosine phosphorylase (MTAP) in hearing: Gene disruption by chromosomal rearrangement in a hearing impaired individual and model organism analysis

C. Morton, M. Liberman, R. Maas, 2007, American journal of medical genetics. Part A.

SUMO1 Haploinsufficiency Leads to Cleft Lip and Palate

Jennifer J. Lund, C. Morton, F. Alkuraya, 2006, Science.

LFA-1 immunodeficiency disease. Definition of the genetic defect and chromosomal mapping of alpha and beta subunits of the lymphocyte function-associated antigen 1 (LFA-1) by complementation in hybrid cells

C. Morton, T. Springer, D. Anderson, 1986, The Journal of experimental medicine.

RSK3 encodes a novel pp90rsk isoform with a unique N-terminal sequence: growth factor-stimulated kinase function and nuclear translocation

S. Weremowicz, C. Morton, Y. Zhao, 1995, Molecular and cellular biology.

Multicolor fluorescence in situ hybridization in clinical cytogenetic diagnostics

C. Morton, E. Lemyre, P. Miron, 2001, Current opinion in pediatrics.

Unrepaired DNA Breaks in p53-Deficient Cells Lead to Oncogenic Gene Amplification Subsequent to Translocations

F. Alt, D. Ferguson, C. Morton, 2002, Cell.

Characterization of the human and rat myoadenylate deaminase genes.

C. Morton, T. Morisaki, P. Clarke, 1990, The Journal of biological chemistry.

Self-injurious behaviours in people with and without intellectual delay: implications for the genetics of suicide.

J. Gusella, C. Morton, C. Ernst, 2010, International Journal of Neuropsychopharmacology.

An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1).

F. Bieber, K. Beisel, S. Weremowicz, 1997, Genomics.

The human cationic amino acid transporter (ATRC1): physical and genetic mapping to 13q12-q14.

L. Cavalli-Sforza, A. Bowcock, R. Eddy, 1992, Genomics.

The human mannose-binding protein gene. Exon structure reveals its evolutionary relationship to a human pulmonary surfactant gene and localization to chromosome 10

C. Morton, G. Bruns, K. Sastry, 1989, The Journal of experimental medicine.

A genetic analysis of taste threshold for phenylthiocarbamide.

R. Cantor, C. Morton, W. Nance, 1981, Acta geneticae medicae et gemellologiae.

Assignment of the human small inducible cytokine A2 gene, SCYA2 (encoding JE or MCP-1), to 17q11.2-12: evolutionary relatedness of cytokines clustered at the same locus.

D. Ledbetter, R. Eddy, T. Shows, 1991, Genomics.

Human ARHGDIG, a GDP-dissociation inhibitor for Rho proteins: genomic structure, sequence, expression analysis, and mapping to chromosome 16p13.3.

S. Weremowicz, C. Morton, D. Higgs, 1998, Genomics.

Description of a case of distal 2p trisomy by array‐based comparative genomic hybridization: A high resolution genome‐wide investigation for chromosomal aneuploidy in a single assay

M. Listewnik, J. Mulliken, C. Morton, 2004, American Journal of Medical Genetics. Part A.

Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.

Saumil N Merchant, Bryan Krastins, Patrick L M Huygen, 2006, Human molecular genetics.

Next-Generation Newborn Hearing Screening

C. Morton, Jun Shen, 2016 .

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

C. Cremers, C. Morton, R. Lifton, 1999, Nature Genetics.

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

S. Bianca, C. Morton, V. Tasic, 2002, Journal of medical genetics.

Novel ATP 6 V 1 B 1 and ATP 6 V 0 A 4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

S. Bianca, C. Morton, V. Tasic, 2002 .

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.

C. Cremers, H. Brunner, C. Morton, 1999, Human molecular genetics.

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

C. Morton, F. Wuyts, E. Fransen, 1999, Human molecular genetics.

Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease.

S. Weremowicz, C. Morton, T. Dryja, 1995, Genomics.

Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9.

Joe C. Adams, J. Aster, C. Lee, 2001, Human molecular genetics.

Structural genomic variation and personalized medicine.

C. Morton, Cynthia C. Morton, Charles Lee, 2008, The New England journal of medicine.

Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.

Ping Liu, J Zhang, C. Morton, 2019, American journal of human genetics.

Genes for the tumor necrosis factors alpha and beta are linked to the human major histocompatibility complex.

W. Fiers, C. Morton, J. Strominger, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Chromosomal location of the genes encoding the leukocyte adhesion receptors LFA-1, Mac-1 and p150,95. Identification of a gene cluster involved in cell adhesion

C. Morton, T. Springer, R. Larson, 1988, The Journal of experimental medicine.

The thrombospondin-4 gene

G. Newton, N. Copeland, D. Gilbert, 1999, Mammalian Genome.

Mutation of perinatal myosin heavy chain associated with a Carney complex variant.

Mark Veugelers, Cynthia C Morton, S. Weremowicz, 2004, The New England journal of medicine.

A role for HLA‐DRB1*1101 and DRB1*0801 in cognitive ability and its decline with age

C. Morton, A. Payton, W. Ollier, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mutations in the protein kinase A R 1 α regulatory subunit cause familial cardiac myxomas and Carney complex Mairead Casy

R. Kucherlapati, K. Montgomery, S. Weremowicz, 2015 .

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.

C. Morton, K. Verhoeven, F. Declau, 2001, Human molecular genetics.

The placental ribonuclease inhibitor (RNH) gene is located on chromosome subband 11p15.5.

S. Weremowicz, C. Morton, E. Fox, 1990, Genomics.

Comprehensive conventional and molecular cytogenetic characterization of B-CPAP, a human papillary thyroid carcinoma-derived cell line.

C. Lee, C. Morton, A. Fusco, 2004, Cancer genetics and cytogenetics.

Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma.

J. Fletcher, S. Weremowicz, C. Morton, 1992, Cancer genetics and cytogenetics.

Cochlin in Normal Middle Ear and Abnormal Middle Ear Deposits in DFNA9 and CochG88E/G88E Mice

C. Morton, A. Giersch, J. O'malley, 2014, Journal of the Association for Research in Otolaryngology.

Identification of Pathogenic Mechanisms of COCH Mutations, Abolished Cochlin Secretion, and Intracellular Aggregate Formation: Genotype–Phenotype Correlations in DFNA9 Deafness and Vestibular Disorder

Jaetae Lee, C. Morton, U. Kim, 2014, Human mutation.

Validation of DNA probes for preimplantation genetic diagnosis (PGD) by fluorescence in situ hybridization (FISH) R1

S. Weremowicz, C. Morton, P. Miron, 2006, Prenatal diagnosis.

Preface

J. Haines, J. Seidman, Douglas R. Smith, 2011 .

Identification of genetically aberrant cell lineages in Wilms' tumors

J. Fletcher, D. Haber, S. Weremowicz, 1994, Genes, chromosomes & cancer.

A neural survival factor is a candidate oncogene in breast cancer

Jennifer Chan, Kornelia Polyak, Andrea Richardson, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Identification, localization, and expression of two novel human genes similar to deoxyribonuclease I.

S. Weremowicz, C. Morton, H. Nomura, 1997, Genomics.

A complement receptor locus: genes encoding C3b/C4b receptor and C3d/Epstein-Barr virus receptor map to 1q32.

C. Morton, G. Bruns, D. Fearon, 1987, Journal of immunology.

Mapping of the human complement factor I gene to 4q25.

K. Buetow, W. Sanger, C. Morton, 1989, Genomics.

Platelet-derived growth factor A chain: gene structure, chromosomal location, and basis for alternative mRNA splicing.

D. Bonthron, S. Orkin, C. Morton, 1988, Proceedings of the National Academy of Sciences of the United States of America.

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

H. Rehm, D. Kolbe, C. Morton, 2021, European Journal of Human Genetics.

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

H. Rehm, D. Kolbe, C. Morton, 2021, European Journal of Human Genetics.

Characterization of familial Waldenstrom's macroglobulinemia.

C. Lee, C. Morton, S. Treon, 2006, Annals of oncology : official journal of the European Society for Medical Oncology.

Genomic organization and chromosomal localization of the DUSP2 gene, encoding a MAP kinase phosphatase, to human 2p11.2-q11.

S. Weremowicz, C. Morton, O. Mcbride, 1995, Genomics.

Human gamma-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7.

T. Waldmann, J. Seidman, T. Shows, 1985, Nature.

STK25 is a candidate gene for pseudopseudohypoparathyroidism.

N. Copeland, D. Gilbert, N. Jenkins, 2001, Genomics.

Psoriasin expression in mammary epithelial cells in vitro and in vivo.

K. Polyak, D. Sgroi, S. Schnitt, 2002, Cancer research.

Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity.

S. Scherer, J. Rosenfeld, L. Shaffer, 2012, Archives of General Psychiatry.

A Sound Foundation Through Early Amplification

M. P. Moeller, Cheryl DeConde Johnson, C. Abdala, 2016 .

Pelvic and pulmonary benign metastasizing leiomyoma: A case report

C. Morton, R. Anchan, P. Bortoletto, 2018, Case reports in women's health.

Trinucleotide Repeats at the rad Locus: Allele Distributions in NIDDM and Mapping to a 3-cM Region on Chromosome 16q

S. Weremowicz, C. Morton, A. Krolewski, 1995, Diabetes.

A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site‐specific vestibular and central oculomotor dysfunction

C. Morton, N. G. Robertson, V. A. Street, 2005, American journal of medical genetics. Part A.

ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice

M. Tekin, C. Morton, X. Liu, 2016, Proceedings of the National Academy of Sciences.

P-243 Significant increase in pregnancy rate achieved by vigorous irrigation of endocervical mucus prior to embryo transfer with the wallace catheter in an IVF-ET program

Thomas T. F. Huang, C. Morton, P. McNamee, 1997 .

Ac ce pt ed m an us cr ip t 1 Cochlin in the eye : functional implications

C. Morton, S. Bhattacharya, T. Cogliati, 2017 .

Cochlin in the eye: Functional implications

C. Morton, S. Bhattacharya, T. Cogliati, 2007, Progress in Retinal and Eye Research.

Human calcium transport protein CaT1.

S. Weremowicz, E. Brown, C. Morton, 2000, Biochemical and biophysical research communications.

A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

Yiping Shen, C. Morton, Hyung-Goo Kim, 2023, Research square.

The gene for the human mast cell high-affinity IgE receptor alpha chain: chromosomal localization to Iq21-q23 and RFLP analysis.

P. Leder, R. Eddy, T. Shows, 1989, American journal of human genetics.

Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel

Andrew R. Grant, H. P. Kang, Marina T. DiStefano, 2018, Genetics in Medicine.

The sequence, expression, and chromosomal localization of a novel polycystic kidney disease 1-like gene, PKD1L1, in human.

S. Weremowicz, C. Morton, Jing Zhou, 2002, Genomics.

Human genes for insulin-like growth factors I and II and epidermal growth factor are located on 12q22----q24.1, 11p15, and 4q25----q27, respectively.

T. Shows, C. Morton, G. Bell, 1986, Cytogenetics and Cell Genetics.

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9.

J. Battey, F. Bieber, S. Weremowicz, 1997, Genomics.

Increasing evidence for syndromic phenotypes associated with RPGR mutations.

A. Swaroop, C. Morton, A. Baldi, 2004, American journal of ophthalmology-glaucoma.

Proteomics Reveal Cochlin Deposits Associated with Glaucomatous Trabecular Meshwork*

C. Morton, Scott D. Smith, S. Bhattacharya, 2005, Journal of Biological Chemistry.

Subcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9

J. Aster, C. Morton, N. G. Robertson, 2003, Journal of medical genetics.

A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domain

G. Vriend, C. Morton, H. Venselaar, 2012, Journal of Molecular Medicine.

Perinatal lethality (ple): a mutation caused by integration of a transgene into distal mouse chromosome 15.

P. Leder, C. Morton, D. Beier, 1989, Genomics.

Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease

H. Rehm, M. C. Brown, D. Corey, 2002, The Journal of Neuroscience.

GENETIC CAUSES OF NON-SYNDROMIC HEARING LOSS

C. Morton, Skvorak G.A.B., 1999 .

AnFiSA: An open-source computational platform for the analysis of sequencing data for rare genetic disease

S. Sunyaev, C. Morton, M. Bouzinier, 2021, medRxiv.

Generation of protective pneumococcal-specific nasal resident memory CD4+ T cells via parenteral immunization

C. Morton, R. Malley, C. Thompson, 2019, Mucosal Immunology.

Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome

D. Behar, C. Morton, A. Ligon, 2013, Clinical case reports.

Identification and characterization of a novel polycystin family member, polycystin-L2, in mouse and human: sequence, expression, alternative splicing, and chromosomal localization.

S. Weremowicz, C. Morton, T. Schreiber, 2000, Genomics.

S. Weremowicz, C. Morton, H. Nomura, 1996, Genomics.

Hereditary leiomyomatosis and renal cell cancer: Cutaneous lesions & atypical fibroids

C. Morton, B. Quade, E. Stewart, 2017, Case reports in women's health.

Position effects of 22q13 rearrangements on candidate genes in Phelan-McDermid syndrome

C. Morton, L. Boccuto, R. Pauly, 2021, PLoS ONE.

ABSENCE OF MAJOR DELETIONS OR REARRANGEMENTS OF CARDIAC MYOSIN HEAVY-CHAIN GENES IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY

J. Seidman, C. Morton, H. Watkins, 1993 .

A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domain

G. Vriend, C. Morton, H. Venselaar, 2012, Journal of Molecular Medicine.

Advances in Brief Psoriasin Expression in Mammary Epithelial Cells in Vitro and in Vivo 1

K. Polyak, D. Sgroi, S. Schnitt, 2001 .

Cochlin Deficiency Protects Against Noise-Induced Hearing Loss

C. Morton, K. Stankovic, N. G. Robertson, 2021, Frontiers in Molecular Neuroscience.

Report of the fourth international workshop on human chromosome 15 mapping 1997.

D. J. Driscoll, S. Christian, T. Lerner, 1999, Cytogenetics and cell genetics.

Complex cytogenetic aberrations in a well-differentiated chondrosarcoma.

J. Fletcher, C. Morton, N. Weidner, 1989, Cancer genetics and cytogenetics.

Clinical picture: Multicolour karyotyping.

C. Lee, C. Morton, L. Wilkins-Haug, 2001, Lancet.

A study of chromium induced allergic contact dermatitis with 54 volunteers: implications for environmental risk assessment.

D. Paustenbach, C. Morton, J. Fowler, 1994, Occupational and environmental medicine.

A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

Yiping Shen, C. Morton, Hyung-Goo Kim, 2023, Scientific reports.

Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and Genomics

S. Schwartz, F. Bieber, R. Stevenson, 2016, Genetics in Medicine.

Characterization of familial Waldenstrom's Macroglobulinemia.

C. Morton, S. Treon, Z. Hunter, 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Genomic structure of the human unconventional myosin VI gene.

C. Morton, N. Ahituv, K. Avraham, 2000, Gene.

Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage.

C. Morton, Joana Fino, D. David, 2023, Gene.

Clinical picture: Multicolour karyotyping.

C. Morton, L. Wilkins-Haug, P. Miron, 2001, Lancet.

Mapping of seven polymorphic loci on human chromosome 13 by in situ hybridization

C. Morton, T. Dryja, 2004, Human Genetics.

Target-enriched massively parallel sequencing for genetic diagnosis of hereditary hearing loss in patients with normal array CGH result.

C. Morton, K. Choy, T. Leung, 2018, Hong Kong medical journal = Xianggang yi xue za zhi.

Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit

Carol M. Hamilton, M. Rice, C. Morton, 2021, Annals of human genetics.

Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.

V. Sheffield, M. Lovett, C. Morton, 1997, Genome research.

A HumanGeneHomologous totheForminGeneResiding attheMurineLimbDeformity Locus: Chromosomal Location andRFLPs

R. Holcombe, C. Morton, R. Maas, 1991 .

Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies.

L. Shaffer, Cheol‐Hee Kim, M. MacDonald, 2012, American journal of human genetics.

ELF4 is fused to ERG in a case of acute myeloid leukemia with a t(X;21)(q25-26;q22).

C. Morton, Steven D. P. Moore, P. Amrein, 2006, Leukemia research.

Disruption of neurexin 1 associated with autism spectrum disorder.

M. Daly, F. Volkmar, M. MacDonald, 2008, American journal of human genetics.

Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries

Toshiro K. Ohsumi, M. Daly, J. Rosenfeld, 2012, Cell.

Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities

J. Gusella, C. Morton, M. Talkowski, 2014, Molecular Psychiatry.

Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity.

S. Scherer, J. Rosenfeld, L. Shaffer, 2012, Archives of general psychiatry.

Intravenous Leiomyomatosis: An Unusual Intermediate between Benign and Malignant Uterine Smooth Muscle Tumors

P. Park, C. Morton, B. Quade, 2016, Modern Pathology.

HumanJchain gene: Chromosomal localization andassociated restriction fragment length polymorphisms

C. Morton, E. E. Max, 1986 .