D. Parry

发表

Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma.

P. Cin, C. Turc‐Carel, F. Li, 1987, Proceedings of the National Academy of Sciences of the United States of America.

The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2

D. Evans, C. Lázaro, G. Rouleau, 2005, Journal of Medical Genetics.

Multiple schwannomas and meningiomas associated with irradiation in childhood.

A. Schneider, D. Parry, C. Abrahams, 1996, Archives of internal medicine.

Genetic linkage studies with neurofibromatosis: the question of heterogeneity.

M. Spence, S. Bale, V. Cortessis, 1987, Journal of medical genetics.

Clinical features distinguish childhood chordoma associated with tuberous sclerosis complex (TSC) from chordoma in the general paediatric population

A. Goldstein, D. Parry, M. McMaster, 2011, Journal of Medical Genetics.

A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.

N. Kley, M. Duyao, J. Rutter, 1993, Cell.

Monozygotic twins discordant for neurofibromatosis 1

Yiping Shen, J. Gusella, R. Foster, 2010, American journal of medical genetics. Part A.

Survival after retinoblastoma: long-term consequences and family history of cancer.

T. Fears, J. Byrne, D. Parry, 1995, Medical and pediatric oncology.

Genetic Variation in the 3′ Untranslated Region of the Neurofibromatosis 1 Gene: Application to Unequal Allelic Expression

J. Gusella, B. Korf, G. Cowley, 1998, Somatic cell and molecular genetics.

Neurofibromatosis type 2 appears to be a genetically homogeneous disease.

J. Haines, R. Martuza, G. Lenoir, 1992, American journal of human genetics.

Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.

M. Kaiser-Kupfer, J. Gusella, M. Maccollin, 1996, American journal of human genetics.

Lens opacities in neurofibromatosis 2: further significant correlations.

M. Kaiser-Kupfer, V. Freidlin, D. Parry, 1993, The British journal of ophthalmology.

Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.

R. Weksberg, G. Rouleau, V. Riccardi, 1996, American journal of human genetics.

Neurofibromatosis 2 (Bilateral Acoustic or Central Neurofibromatosis), a Treatable Cause of Deafness

M. Kaiser-Kupfer, D. Parry, R. Eldridge, 1991 .

A point mutation associated with a severe phenotype of neurofibromatosis 2

J. Gusella, R. Ojemann, D. Viskochil, 1996, Annals of neurology.

Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma

F. Couch, S. Chanock, M. Yeager, 2022, Human mutation.

Allelic expression of the NF2 gene in neurofibromatosis 2 and schwannomatosis

J. Gusella, L. Kluwe, M. Maccollin, 1999, Neurogenetics.

Vestibular schwannoma (acoustic neuroma). Consensus development conference.

D. Parry, R. Eldridge, 1992, Neurosurgery.

Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1).

J. Haines, M. Pericak-Vance, B. Korf, 1989, American journal of human genetics.

Intramedullary and spinal canal tumors in patients with neurofibromatosis 2: MR imaging findings and correlation with genotype.

N. Patronas, M. Maccollin, D. Parry, 2001, Radiology.

Symposium on Linkage of von Recklinghausen Neurofibromatosis (NF1). Closing in on the gene for von Recklinghausen neurofibromatosis.

J. Mulvihill, D. Parry, 1987, Genomics.

Predictors of vestibular schwannoma growth in patients with neurofibromatosis Type 2.

E. Makariou, M. Baser, D. Parry, 2002, Journal of neurosurgery.

Regulatory de novo mutations underlying intellectual disability

Inês Cebola, A. Lampe, D. Moore, 2022, Life Science Alliance.

Sarcomas in a child and her father: an etiologic consultation.

J. Mulvihill, D. Parry, R. W. Miller, 1979, American journal of diseases of children.

Baseline and mutagen-induced sister-chromatid exchanges in cultures of human whole blood and purified fresh or frozen lymphocytes.

J. Mulvihill, S. Galloway, D. Parry, 1987, Mutation research.

Segmental aneuploidy and the genetic gross structure of the Drosophila genome.

B. S. Baker, B. K. Davis, G. L. Miklos, 1972, Genetics.

CROSSING OVER NEAR THE CENTROMERE OF CHROMOSOME 3 IN DROSOPHILA MELANOGASTER FEMALES.

D. Suzuki, D. Parry, 1964, Genetics.

The association of posterior capsular lens opacities with bilateral acoustic neuromas in patients with neurofibromatosis type 2.

Manuel B. Datiles III, M. Kaiser-Kupfer, P. Edwards, 1989, Archives of ophthalmology.

Neurofibromatosis type 2

J. Butman, R. Lonser, D. Parry, 2009, The Lancet.

NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update.

M. Kaiser-Kupfer, J. Mulvihill, D. Parry, 1990, Annals of internal medicine.

Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications.

J. Mulvihill, H. Andersson, D. Parry, 1995, American journal of medical genetics.

Chordoma: incidence and survival patterns in the United States, 1973–1995

A. Goldstein, D. Parry, M. McMaster, 2004, Cancer Causes & Control.

Relationship between head circumference and height in normal adults and in the nevoid basal cell carcinoma syndrome and neurofibromatosis type I.

C. Amos, S. Bale, D. Parry, 1991, American journal of medical genetics.

Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndrome.

S. Bale, J. Mulvihill, D. Parry, 1989, Cancer genetics and cytogenetics.

THE DISTRIBUTION AND DIFFERENTIATION OF LYMPH‐BORNE IMMUNOBLASTS AFTER INTRAVENOUS INJECTION INTO SYNGENEIC RECIPIENTS

J. Hall, D. Parry, D. Parry, 1972, Cell and tissue kinetics.

Waardenburg-like features with cataracts, small head size, joint abnormalities, hypogonadism, and osteosarcoma.

J. Mulvihill, A. Safyer, D. Parry, 1978, Journal of medical genetics.

Sites of [3H]taurine Uptake in the Rat Substantia Nigra in Relation to the Release of Taurine from the Striatonigral Pathway

A. D. Smith, J. Bolam, D. Parry, 1990, The European journal of neuroscience.

Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

S. Pulst, K. Hoang-Xuan, G. Thomas, 1993, Nature.

A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

J. Haines, M. MacDonald, R. Martuza, 1993, Cell.

SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma.

M. Kaiser-Kupfer, J. Mulvihill, D. Parry, 1986, American journal of medical genetics.

Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma

Jianxin Shi, S. Chanock, M. Yeager, 2014, Human Genetics.

Neurofibromatosis type 1 (Recklinghausen's disease). Neurologic and cognitive assessment with sibling controls.

J. Dambrosia, M. Kaiser-Kupfer, M. Denckla, 1989, American journal of diseases of children.

Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene

M. Pericak-Vance, M. Spence, R. Martuza, 1987, Cell.

Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival

X. Hua, Jianxin Shi, A. Goldstein, 2021, Nature Communications.

Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2)

Yinshan Zhao, G. Rouleau, G. Rouleau, 2002, Genetic epidemiology.

Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity.

M I Kaiser-Kupfer, M. Kaiser-Kupfer, N. Patronas, 1994, American journal of medical genetics.

Strategies for controlling cancer through genetics.

J. Mulvihill, D. Parry, R. W. Miller, 1987, Cancer research.

Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.

J J Mulvihill, D E Goldgar, P. Green, 1989, American journal of human genetics.

Whole genome sequencing of mutation-negative individuals with Cornelia de Lange Syndrome

K. Prescott, S. Holden, N. Whiffin, 2022, medRxiv.

Linkage analysis of neurofibromatosis (von Recklinghausen disease).

M. Spence, L. Field, A. Rubenstein, 1983, Journal of medical genetics.

Recklinghausen disease ) . neurofibromatosis ( von Linkage analysis of

M. Spence, L. Field, A. Rubenstein, 2022 .

Loss of heterozygosity for the NF2 gene in retinal and optic nerve lesions of patients with neurofibromatosis 2

M. Kaiser-Kupfer, A. Vortmeyer, D. Gutmann, 2002, The Journal of pathology.

The parental origin of new mutations in neurofibromatosis 2

J. Gusella, L. Kluwe, V. Mautner, 2000, Neurogenetics.

Methodological issues in longitudinal studies: vestibular schwannoma growth rates in neurofibromatosis 2

D. Evans, V. Mautner, M. Baser, 2005, Journal of Medical Genetics.

Clinical findings in families with chordoma with and without T gene duplications and in patients with sporadic chordoma reported to the Surveillance, Epidemiology, and End Results program.

A. Goldstein, N. Patronas, M. Quezado, 2020, Journal of neurosurgery.

T (brachyury) gene duplication confers major susceptibility to familial chordoma

A. Goldstein, M. Kelley, D. Alcorta, 2009, Nature Genetics.

Advances in Neurofibromatosis 2 (NF2): A Workshop Report

E. A. Chiocca, W. J. Ramsey, S. Pulst, 2000, Journal of neurogenetics.

FAMILIAL OCCURRENCE OF COMBINED PIGMENT EPITHELIAL AND RETINAL HAMARTOMAS ASSOCIATED WITH NEUROFIBROMATOSIS 2

M. Kaiser-Kupfer, D. Parry, E. Bouzas, 1992, Retina.

Visual impairment in patients with neurofibromatosis 2

M. Kaiser-Kupfer, D. Parry, E. Bouzas, 1993, Neurology.

Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17.

J. Haines, M. Pericak-Vance, B. Korf, 1987, Genomics.

Incidence of and Neurodevelopmental Outcomes After Late-Onset Meningitis Among Children Born Extremely Preterm

R. J. Williams, Eugenia K. Pallotto, Margaret M. Crawford, 2022, JAMA network open.

Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markers

J. Dumanski, G. Rouleau, G. Lenoir, 1993, Neurology.

Repair of sister-chromatid exchange-inducing lesions in mutagen-treated cultures of human whole blood and purified fresh or frozen lymphocytes.

J. Mulvihill, S. Galloway, D. Parry, 1988, Mutation research.

Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7q33.

A. Goldstein, M. Kelley, E. Sheridan, 2001, American journal of human genetics.

The Niikawa-Kuroki (Kabuki make-up) syndrome in an American black.

M. Kaiser-Kupfer, J. Mulvihill, D. Parry, 1986, American journal of ophthalmology.

A meiotic mutant affecting recombination in female Drosophila melanogaster.

D. Parry, 1973, Genetics.

Carotid body tumors in humans: genetics and epidemiology.

L. Strong, S. Grufferman, J. Carney, 1982, Journal of the National Cancer Institute.

Multiple schwannomas and meningiomas associated with irradiation in childhood.

A. Schneider, D. Parry, C. Abrahams, 1996, Archives of internal medicine.

Familial Sotos syndrome (cerebral gigantism): craniofacial and psychological characteristics.

J. Mulvihill, D. Parry, A. Bale, 1985, American journal of medical genetics.

Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma

Jianxin Shi, S. Chanock, M. Yeager, 2014, Human Genetics.

Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility

S. Chanock, M. Yeager, N. Freedman, 2021, Cancers.

Corroboration of a familial chordoma locus on chromosome 7q and evidence of genetic heterogeneity using single nucleotide polymorphisms (SNPs)

S. Chanock, A. Goldstein, A. Bergen, 2005, International journal of cancer.

Genetic Linkage Analysis of Neurofibromatosis a

M. Spence, M. Marazita, J. Mulvihill, 1986, Annals of the New York Academy of Sciences.

Genetic Linkage Analysis of Neurofibromatosis with DNA Markers a

M. Spence, T. Gilliam, J. Gusella, 1986, Annals of the New York Academy of Sciences.

Strategies for controlling cancer through genetics: report of a workshop.

J. Mulvihill, D. Parry, R. W. Miller, 1987, American journal of human genetics.

Laminar organization of spinal dorsal horn neurones activated by C- vs. A-heat nociceptors and their descending control from the periaqueductal grey in the rat

B. Lumb, D. Parry, S. Koutsikou, 2007, The European journal of neuroscience.

Gene expression profiling identifies two chordoma subtypes associated with distinct molecular mechanisms and clinical outcomes.

Tengyu Ma, S. Chanock, A. Goldstein, 2022, Clinical cancer research : an official journal of the American Association for Cancer Research.

Ultrastructural Evidence for Changes in Synaptic Input to the Hypothalamic Luteinizing Hormone‐Releasing Hormone Neurons in Photosensitive and Photorefractory Starlings

A. Goldsmith, D. Parry, D. Parry, 1993, Journal of neuroendocrinology.

Clinical findings in chordoma families with and without T gene duplications and chordoma patients reported to the Surveillance, Epidemiology and End Results Program

A. Goldstein, M. Quezado, D. Parry, 2021 .

Neurofibromatosis type 2.

J. Butman, R. Lonser, D. Parry, 2009, Lancet.

Chromatid repulsion associated with Roberts/SC phocomelia syndrome is reduced in malignant cells and not expressed in interspecies somatic-cell hybrids.

U. Francke, D. Parry, J. Cowan, 1986, American journal of human genetics.

The Origin of Multiple Crossover Chromatids in Short Genetic Intervals in DROSOPHILA MELANOGASTER.

D. Suzuki, D. Baillie, D. Parry, 1966, Genetics.

Vestibular schwannoma (acoustic neuroma). Consensus development conference.

D. Parry, R. Eldridge, 1992, Neurosurgery.

The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2

C. Lázaro, G. Rouleau, R. Ramsden, 2005, Journal of Medical Genetics.

Neurofibromatosis Type 2: MR Evaluation and Clinical Correlation

M. Kaiser-Kupfer, D. Parry, R. Eldridge, 1989 .

Radiosensitivity of skin fibroblasts from atomic bomb survivors with and without breast cancer.

R. Setlow, G. Beebe, M. Bender, 1990, Cancer research.