Professor Emeritus
Pediatrics - Fresno
+1 559 227-4472
Dr. Curry is an emeritus tenured UCSF Professor. of Pediatrics She continues to be active in both clinical and academic genetics. Dr. Curry is a graduate of Yale University School of Medicine and is Board Certified in Pediatrics and Clinical Genetics. Her research interests include syndrome delineation in the fetus and newborn, and causes of intellectual disability. She has held many national positions in both genetics and pediatrics and speaks nationally and internationally..
Publications
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Genetics in medicine : official journal of the American College of Medical Genetics
The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients.
European journal of human genetics : EJHG
Personal journeys to and in human genetics and dysmorphology.
American journal of medical genetics. Part A
Correction: Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.
European journal of human genetics : EJHG
Ear anomalies and hearing loss in patients with VACTERL association and the effect of maternal diabetes.
American journal of medical genetics. Part A
Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families.
American journal of medical genetics. Part A
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype.
American journal of human genetics
Dominant ARF3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafish.
Nature communications
Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.
American journal of medical genetics. Part A
Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.
European journal of human genetics : EJHG
ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies.
American journal of human genetics
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Brain : a journal of neurology
Thinking outside "The Box": Case-based didactics for medical education and the instructional legacy of Dr John M. Graham, Jr.
American journal of medical genetics. Part A
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2.
Clinical genetics
The spectrum of brain malformations and disruptions in twins.
American journal of medical genetics. Part A
Recurrent constellations of embryonic malformations re-conceptualized as an overlapping group of disorders with shared pathogenesis.
American journal of medical genetics. Part A
Correction: Addendum: ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.
Genetics in medicine : official journal of the American College of Medical Genetics
Addendum: ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.
Genetics in medicine : official journal of the American College of Medical Genetics
Expanding Clinical Presentations Due to Variations in THOC2 mRNA Nuclear Export Factor.
Frontiers in molecular neuroscience
Redefining the Etiologic Landscape of Cerebellar Malformations.
American journal of human genetics
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies.
American journal of human genetics
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
European journal of medical genetics
Expansion of the phenotype of Kosaki overgrowth syndrome.
American journal of medical genetics. Part A
A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome.
American journal of human genetics
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations.
Journal of medical genetics
A novel mutation in two Hmong families broadens the range of STRA6-related malformations to include contractures and camptodactyly.
American journal of medical genetics. Part A
Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan type.
Journal of medical genetics
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypes.
Human mutation
A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases.
Cell
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
American journal of human genetics
Mutations in PIK3R1 cause SHORT syndrome.
American journal of human genetics
The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
American journal of medical genetics. Part A
WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta.
The New England journal of medicine
ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.
Genetics in medicine : official journal of the American College of Medical Genetics
Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm.
Nature genetics
Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsis.
American journal of medical genetics. Part A
Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region.
American journal of medical genetics. Part A
Ehlers-Danlos syndrome type VIII is clinically heterogeneous disorder associated primarily with periodontal disease, and variable connective tissue features.
European journal of human genetics : EJHG
Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling.
American journal of human genetics
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.
Human mutation
Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature.
American journal of medical genetics. Part C, Seminars in medical genetics
Elements of morphology: standard terminology for the lips, mouth, and oral region.
American journal of medical genetics. Part A
Chondrodysplasia punctata associated with maternal autoimmune diseases: expanding the spectrum from systemic lupus erythematosus (SLE) to mixed connective tissue disease (MCTD) and scleroderma report of eight cases.
American journal of medical genetics. Part A
Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation?
American journal of medical genetics. Part A
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.
American journal of medical genetics. Part A
Mutations in the pericentrin (PCNT) gene cause primordial dwarfism.
Science (New York, N.Y.)
Diaphanospondylodysostosis: six new cases and exclusion of the candidate genes, PAX1 and MEOX1.
American journal of medical genetics. Part A
Risk factors for perinatal arterial stroke: a study of 60 mother-child pairs.
Pediatric neurology
Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.
American journal of medical genetics. Part A
Mental retardation: diagnosis, management, and family support.
Current problems in pediatric and adolescent health care
Introduction to Judith Hall Festschrift.
American journal of medical genetics. Part A
Schizencephaly: heterogeneous etiologies in a population of 4 million California births.
American journal of medical genetics. Part A
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
American journal of human genetics
Neonatal phenotype in Kabuki syndrome.
American journal of medical genetics. Part A
A tribute to Bryan D. Hall: Festschrift 2003.
American journal of medical genetics. Part A
Hypospadias in California: trends and descriptive epidemiology.
Epidemiology (Cambridge, Mass.)
Spectrum of dolichospondylic dysplasia: two new patients with distinctive findings.
American journal of medical genetics
Rational evaluation of the adolescent with mental retardation.
Adolescent medicine (Philadelphia, Pa.)
Fungal septicemia in patients receiving parenteral hyperalimentation.
The New England journal of medicine