Vincent Michael Riccardi
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Vincent Michael Riccardi's Degrees
- Bachelors Biology University of California, Berkeley
- Doctorate Medicine University of California, San Francisco
- PhD Genetics University of California, San Francisco
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(Suggest an Edit or Addition)Vincent Michael Riccardi's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion. (1978) (676)
- Neurofibromatosis: Phenotype, Natural History and Pathogenesis (1992) (601)
- Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. (1981) (587)
- Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis. (1990) (398)
- Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13. (1979) (381)
- An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation. (2007) (326)
- Neurofibromatosis: clinical heterogeneity. (1982) (287)
- Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. (1996) (264)
- Malignant peripheral nerve sheath tumors in neurofibromatosis 1. (2000) (247)
- Cognitive function and academic performance in neurofibromatosis. 1: consensus statement from the NF1 Cognitive Disorders Task Force. (1997) (246)
- Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases. (1982) (238)
- Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors. (1987) (226)
- Distinctive Cancer Associations in Patients With Neurofibromatosis Type 1. (2016) (221)
- von Recklinghausen neurofibromatosis. II. Incidence of optic gliomata. (1984) (213)
- Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients. (1994) (211)
- Neurofibromatosis: past, present, and future. (1991) (159)
- Familial cavernous angiomas: natural history and genetic study over a 5-year period. (1982) (158)
- Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation. (1981) (150)
- Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation (2021) (148)
- Reduction of biogenic amine levels in the Rett syndrome. (1985) (146)
- Neurofibromatosis: oral and radiographic manifestations. (1984) (134)
- The aniridia-Wilms tumor association: The critical role of chromosome band 11p13☆ (1980) (130)
- Angiogenic and invasive properties of neurofibroma Schwann cells (1990) (122)
- Penetrance of von Recklinghausen neurofibromatosis: a distinction between predecessors and descendants. (1988) (116)
- Mast-cell stabilization to decrease neurofibroma growth. Preliminary experience with ketotifen. (1987) (113)
- Amniotic Fluid Concentrations of Δ5 and Δ4 Steroids in Fetuses with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Deficiency and in Anencephalic Fetuses (1980) (108)
- Von Recklinghausen neurofibromatosis. Incidence of iris hamartomata. (1981) (95)
- Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor. (1987) (95)
- Trisomy 8: an international study of 70 patients. (1977) (94)
- Type 1 neurofibromatosis and the pediatric patient. (1992) (89)
- Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11 (1988) (86)
- Genetic mosaicism in normal tissues of Wilms' tumour patients (1993) (79)
- Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas (1979) (77)
- Pathophysiology of neurofibromatosis. IV. Dermatologic insights into heterogeneity and pathogenesis. (1980) (74)
- A controlled multiphase trial of ketotifen to minimize neurofibroma-associated pain and itching. (1993) (74)
- Associations of clinical features in neurofibromatosis 1 (NF1) (2000) (71)
- Neurofibromatosis: a neoplastic birth defect with two age peaks of severe problems. (1977) (70)
- MR imaging of optic pathways in patients with neurofibromatosis. (1987) (68)
- Aniridia caused by a heritable chromosome 11 deletion. (1979) (67)
- Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism. (1992) (67)
- Ocular Abnormalities in Neurofibromatosis 2 (1995) (66)
- Gene dose effect: intraband mapping of the LDH A locus using cells from four individuals with different interstitial deletions of 11p. (1977) (64)
- The pathophysiology of neurofibromatosis: IX. Paternal age as a factor in the origin of new mutations. (1984) (63)
- Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteria. (1980) (63)
- Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomes (2004) (61)
- The Perlman familial nephroblastomatosis syndrome. (1986) (60)
- Cutaneous manifestation of neurofibromatosis: cellular interaction, pigmentation, and mast cells. (1981) (57)
- Rett syndrome: initial experience with an emerging clinical entity. (1985) (53)
- The FG syndrome: further characterization, report of a third family, and of a sporadic case. (1977) (49)
- Congenital hydrocephalus and cerebellar agenesis (1978) (49)
- The ocular presentation of neurofibromatosis 2 (1997) (48)
- Parental origin of de novo constitutional deletions of chromosomal band 11p13. (1990) (48)
- Recent developments in neurofibromatoses and RASopathies: Management, diagnosis and current and future therapeutic avenues (2015) (48)
- Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome. (1982) (47)
- Spondylohumerofemoral hypoplasia (giant cell chondrodysplasia): a neonatally lethal short-limbed skeletal displasia. (1982) (47)
- Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2. (1980) (46)
- Ocular abnormalities in neurofibromatosis 2. (1996) (45)
- Phenotypic variability in monozygotic twins with neurofibromatosis 2. (1996) (43)
- Possible misdiagnosis of Krabbe disease. (1976) (43)
- Paternal age and sporadic neurofibromatosis 1: A case‐control study and consideration of the methodologic issues (1997) (43)
- Multiple cytogenetic aberrations in neurofibrosarcomas complicating neurofibromatosis. (1986) (42)
- Chromosome translocations in couples with multiple spontaneous abortions. (1982) (42)
- Neurofibromatosis Type 1—An Update and Review for the Primary Pediatrician (1996) (42)
- Cutaneous neurofibromas (2018) (40)
- Duplication of proximal 15q as a cause of Prader-Willi syndrome. (1987) (39)
- The Rett syndrome: genetics and the future. (1986) (39)
- Ring chromosome 15: phenotype, Ag-NOR analysis, secondary aneuploidy, and associated chromosome instability. (1980) (38)
- Neurofibromatosis type 1 is a disorder of dysplasia: the importance of distinguishing features, consequences, and complications. (2009) (37)
- Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinations (1996) (37)
- The genetic predisposition to and histogenesis of neurofibromas and neurofibrosarcoma in neurofibromatosis type 1. (2007) (37)
- Independent NF1 mutations in two large families with spinal neurofibromatosis (2003) (35)
- The Multiple Forms of Neurofibromatosis (1982) (34)
- Café au lait spots: the pediatrician's perspective. (2001) (34)
- Absent patellae, mild mental retardation, skeletal and genitourinary anomalies, and C group autosomal mosaicism. (1970) (34)
- Acute leukemia associated with trisomy 8 mosaicism and a familial translocation 46,XY,t(7;20)(p13;p12). (1978) (34)
- Anencephaly with incomplete twinning (diprosopus). (1977) (34)
- Neurofibromatosis in Gothenburg, Sweden. III. Psychiatric and social aspects. (1989) (34)
- Genetic differentiation of bicolor damselfish (Eupomacentrus partitus) populations in the Florida Keys (1989) (34)
- Neurofibrosarcoma as a complication of von Recklinghausen neurofibromatosis. (1989) (33)
- A discordant sibship analysis between beta-NGF and neurofibromatosis. (1985) (31)
- Linkage studies with chromosome 17 DNA markers in 45 neurofibromatosis 1 families. (1987) (31)
- ASHG activities relative to education: Human genetics as a component of medical school curricula: A report to the American society of human genetics. (1988) (30)
- Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancer (2001) (30)
- Cutaneous neuro fi bromas Current clinical and pathologic issues (29)
- Different Patterns of Mast Cells Distinguish Diffuse from Encapsulated Neurofibromas in Patients with Neurofibromatosis 1 (2011) (29)
- Encephalocraniocutaneous lipomatosis. Report of two cases and a review of the literature. (1989) (28)
- Neurofibromatosis and related tumors. Natural occurrence and animal models. (1994) (28)
- Serum neuronal growth factor levels in von Recklinghausen's neurofibromatosis (1984) (27)
- Familial multiple cafe au lait spots. (1994) (26)
- Guidelines of care for neurofibromatosis type 1 (1997) (26)
- Ketotifen suppression of NF1 neurofibroma growth over 30 years (2015) (26)
- Communication and Counseling in Health Care (1983) (26)
- Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomes (1982) (26)
- The pathophysiology of neurofibromatosis. II. Angiosarcoma as a complication. (1984) (26)
- The prune belly anomaly: heterogeneity and superficial X-linkage mimicry. (1977) (26)
- Discounting an adverse maternal effect on severity of neurofibromatosis. (1987) (24)
- A syndrome of microcephaly and retinal pigmentary abnormalities without mental retardation in a family with coincidental autosomal dominant hyperreflexia. (1984) (24)
- Chromosomal abnormalities associated with congenital contractures (arthrogryposis) (1985) (24)
- Duplication 11p11.3 14.1 to meiotic crossing-over (1980) (23)
- Growth‐Promoting Factors in Neurofibroma Crude Extracts a (1986) (23)
- The importance of advanced parental age in the origin of neurofibromatosis type 1 (2012) (23)
- Considerations for development of therapies for cutaneous neurofibroma (2018) (23)
- Familial Helicobacter pylori Infection: Societal Factors, Human Genetics, and Bacterial Genetics (1994) (22)
- Neurofibromatosis and Albright's syndrome. (1987) (22)
- Neurofibromatosis: variable expression is not intrinsic to the mutant gene. (1979) (22)
- Amniotic fluid concentrations of delta 5 and delta 4 steroids in fetuses with congenital adrenal hyperplasia due to 21 hydroxylase deficiency and in anencephalic fetuses. (1980) (22)
- The Genetic Approach to Human Disease (1977) (21)
- The familial occurrence of Poland syndrome. (1977) (21)
- Genotype, malleotype, phenotype, and randomness: lessons from neurofibromatosis-1 (NF-1) (1993) (21)
- Brief clinical report: aqueductal stenosis leading to hydrocephalus--an unusual manifestation of neurofibromatosis. (1983) (20)
- Catalase levels in patients with aniridia and/or Wilms' tumor: utility and limitations. (1981) (19)
- Clinical characteristics predicting internal neurofibromas in 357 children with neurofibromatosis-1: results from a cross-selectional study (2012) (19)
- The biology of cutaneous neurofibromas (2018) (18)
- Genetic analysis of eight loci tightly linked to neurofibromatosis 1. (1989) (17)
- Neurofibromatosis in Gothenburg, Sweden. II. Intellectual compromise. (1989) (17)
- Mapping parathyroid hormone, β-globin, insulin, and LDH-A genes within the human chromosome 11 short arm by spot blotting sorted chromosomes (2004) (16)
- 49,XXXXY chromossomal anomaly in a neonate. (1971) (16)
- Histogenesis control genes and neurofibromatosis 1 (2000) (16)
- Unilateral gluteal hypoplasia and brachysyndactyly: lower extremity counterpart of the Poland anomaly. (1978) (15)
- Triplication of chromosome arm 20p due to inherited translocation and secondary nondisjunction. (1979) (15)
- Update from the 2013 international neurofibromatosis conference (2014) (15)
- Lower fasting blood glucose in neurofibromatosis type 1 (2015) (15)
- Report of the Task Force on Teaching Human Genetics in North American Medical Schools. (1989) (15)
- Methods for rapid detection of a recurrent nonsense mutation and documentation of phenotypic features in neurofibromatosis type 1 patients (1995) (14)
- Cognitive function and academic performance in neurofibrornatosis 1 (1997) (14)
- Phenotype associated with ring 10 chromosome: report of patient and review of literature. (1981) (14)
- Brachydactyly, type E: hereditary shortening of digits, metacarpals, metatarsals, and long bones. (1974) (14)
- The Turner syndrome and the Y chromosome: mechanisms of diminished Y-determined maleness. (1978) (13)
- Analysis of neurofibromatosis 1 (NF1) lesions by body segment (2004) (13)
- Multisystem burden of neurofibromatosis 1 in Denmark: registry- and population-based rates of hospitalizations over the life span (2020) (13)
- The pathophysiology of neurofibromatosis (1980) (12)
- Health care and disease prevention through genetic counseling: a regional approach. (1976) (12)
- Von Recklinghausen neurofibromatosis and genetic linkage studies: clinical considerations. (1987) (12)
- Duplications, deletions, and single-nucleotide variations: the complexity of genetic arithmetic (2012) (12)
- A genetic linkage study in 15 families of individuals with von Recklinghausen neurofibromatosis. (1985) (12)
- Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomes. (1982) (12)
- The Prenatal Diagnosis of NF‐1 and NF‐2 (1992) (11)
- Neurofibromatosis in a patient with systemic lupus erythematosus. (1983) (11)
- Hereditary pancreatitis. Nonspecificity of aminoaciduria and diagnosis of occult disease. (1975) (11)
- Partial trisomy of chromosome 14: (+14q-). (1976) (11)
- The evolution and multi-molecular properties of NF1 cutaneous neurofibromas originating from C-fiber sensory endings and terminal Schwann cells at normal sites of sensory terminations in the skin (2019) (11)
- Chromosome 8 abnormalities as components of neoplastic and hematologic disorders (1979) (11)
- Non-von Recklinghausen's neurofibromatosis presenting as hemifacial neurofibromas and contralateral café au lait spots. (1987) (11)
- Hereditary Pancreatitis: Nonspecificity of Aminoaciduria and Diagnosis of Occult Disease (1975) (11)
- Adaptation in Lesch-Nyhan cells exposed to aminopterin. (1972) (10)
- Neurofibromatosis: an overview and new directions in clinical investigations. (1981) (10)
- An autosomal dominant inheritance for multiple sunlight-induced malignancy in a patient without abnormalities in DNA repair or replication. Repository identification No. GM2881. (1981) (10)
- Vascular changes in cutaneous neurofibromas. (1986) (10)
- Of mass and men: neurofibromas and histogenesis. (2000) (10)
- The gene for a novel epidermal antigen maps near the neurofibromatosis 1 gene. (1992) (10)
- Karyotype-phenotype correlation: Mosaic trisomy 8 and partial trisomies of different segments of chromosome 8 (1978) (9)
- Linkage relationships of the gene for the beta subunit of nerve growth factor (NGFB) with other chromosome 1 marker loci. (1985) (9)
- Controversy in the management of optic pathway gliomas. 29 patients treated with radiation therapy at Baylor College of Medicine from 1967 through 1987. (1988) (9)
- Neurofibromatosis. The importance of localized or otherwise atypical forms. (1987) (9)
- Prenatal diagnosis of congenital adrenal hyperplasia. (1979) (9)
- Neurofibromatosis heterogeneity. (1984) (9)
- The 11q- syndrome (1977) (9)
- Histogenesis control genes: embryology, wound-healing, and NF1. (2000) (9)
- Neurofibromatosis as a Model for Investigating Hereditary vs. Environmental Factors in Learning Disabilities (1985) (8)
- De novo 13q paracentric inversion in a boy with cleft palate and mental retardation (1979) (8)
- Prevalence and clinicopathological characteristics of lipomatous neurofibromas in neurofibromatosis 1: An investigation of 229 cutaneous neurofibromas and a systematic review of the literature (2018) (8)
- The use of subchromosome-length unique band sequences in the analysis of prophase chromosomes. (1988) (8)
- Genetic etiology of retinoblastoma. (1978) (8)
- American paternal age data for selected years from 1876 to 1981. (1988) (8)
- Neuronal Growth Factors from Tumours of Von Recklinghausen Neurofibromatosis (1987) (8)
- Cell--cell interaction as an epigenetic determinant in the expression of mutant neural crest cells. (1979) (7)
- S100B and neurofibromin immunostaining and X‐inactivation patterns of laser‐microdissected cells indicate a multicellular origin of some NF1‐associated neurofibromas (2011) (7)
- Characteristics of skin and tumor fibroblasts from neurofibromatosis patients. (1981) (7)
- Current Utilization of Mast Cell Stabilizers for Preemptive Treatment of NF1 Neurofibromas (2015) (7)
- Prophase chromosome unique band sequences: definition and utilization. (1986) (7)
- The path forward: 2015 International Children's Tumor Foundation conference on neurofibromatosis type 1, type 2, and schwannomatosis (2017) (7)
- Hair Whorl as an Indicator of a Mediastinal Plexiform Neurofibroma (1997) (7)
- Possible genetic etiology of damselfish neurofibromatosis: genetic differentiation of bicolor damselfish (Pomacentrus partitus) populations. (1988) (6)
- “Neurofibromatosis (Von Recklinghausen's disease): A clinical‐psychiatric and genetic study.” Birgitta Samuelsson, M. D. Psychiatric Department III, University of Göteborg, Lilliagen's Hospital, Göteborg, Sweden (1982) (6)
- Ambiguous genitalia in the Russell-Silver syndrome. (1978) (6)
- Neurofibromatosis update. (1989) (6)
- Diagnostic and management considerations posed by multiple café au lait spots. (2009) (6)
- Skin, blood, nerve cells, and heritability. New lessons from neurofibromatosis type 1. (1995) (6)
- Absence of association of HTLV‐I infection with type 1 neurofibromatosis in the United States or Japan (1991) (5)
- Clinical genetics and genetic counseling. (1982) (5)
- Genetic alterations and growth factors in the pathogenesis of von Recklinghausen neurofibromatosis. (1989) (5)
- Genetic heterogeneity of aniridia: negative linkage data. (1980) (5)
- Linkage Analysis between the β‐Nerve Growth Factor Gene and Other Chromosome lp Markers and Disseminated Neurofibromatosis a (1986) (5)
- Late sequelae of aberrant intrauterine bands (1974) (5)
- De nova astrocytoma following immunosuppression in neurofibromatosis (1990) (5)
- Guidelines of care for neurofibromatosis type 1. American Academy of Dermatology Guidelines/Outcomes Committee. (1997) (5)
- Psychiatric disorders in individuals with neurofibromatosis 1 in Denmark: A nationwide register‐based cohort study (2021) (4)
- Early manifestations of neurofibromatosis: diagnosis and management. (1982) (4)
- Molecular biology of the neurofibromatoses. (1993) (4)
- Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes. (1987) (4)
- Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia. (1991) (4)
- Chapter 2 – Neurofibromatosis (1987) (4)
- Twin recurrence and amniocentesis: male and MZ heritability factors. (1978) (4)
- INVITEDEDITORIAL Genotype, Malleotype, Phenotype, andRandomness: Lessons from Neurofibromatosis- I(NF-I) (1993) (4)
- Human genetics teaching. (1990) (4)
- Neurofibromin Deficiency and Extracellular Matrix Cooperate to Increase Transforming Potential through FAK-Dependent Signaling (2021) (4)
- Chromosomes, embryonal tumors, and birth defects. (1980) (4)
- Denervation in von Recklinghausen's neurofibromatosis (NF‐1) leads to fewer and smaller neurofibromas (1988) (3)
- Preventive medicine through genetic counseling: a regional program. (1975) (3)
- The E7-associated cell-surface antigen: a marker for the 11p13 chromosomal deletion associated with aniridia-Wilms tumor. (1985) (3)
- Low X-chromatin frequency in congenital adrenal hyperplasia. (1972) (3)
- Amusia and its electrophysiological correlates in neurofibromatosis type 1. (2018) (3)
- Duplication 11p11.3 leads to 14.1 to meiotic crossing--over. (1980) (3)
- Genetic counseling as part of hospital care. (1978) (3)
- Apolipoprotein E synthesis in neurofibrosarcoma and schwannoma cell cultures from two individuals with neurofibromatosis (1987) (3)
- Structural alteration of lung parenchyma in patients with NF1: a phenotyping study using multidetector computed tomography (MDCT) (2021) (3)
- von Recklinghausen Disease: 130 Years (2012) (3)
- Expression of selected growth factors and oncogenes in neurofibrosarcomas complicating von Recklinghausen disease. (1988) (3)
- Neurofibromatosis classification clarified. (1989) (3)
- Piebaldism and Neurofibromatosis 1 (1993) (2)
- Hiding in Plain Sight: A Consideration of NF1-Associated Hypovitaminosis D and its Treatment (2014) (2)
- Neurofibromatosis mimicry. (1991) (2)
- Ketotifen, mast cells and NF1 cutaneous neurofibromas: Compelling human data (2020) (2)
- Neurofibromatosis: challenges for applied cellular and molecular biology. (1988) (2)
- Syndromology gone awry--the phenotypic overlap of NF-1 with the Noonan syndrome. (1989) (2)
- Hypomelanosis of Ito and ectrodactyly. (1980) (2)
- Neurofibromatosis (von Recklinghausen disease) : genetics, cell biology, and biochemistry (1981) (2)
- Screening school-aged children for neurofibromatosis 1: dermatology or economics and public policy? (2005) (2)
- Problems in diagnosing neurofibromatosis. (1981) (2)
- Aniridia, cataracts, and Wilms tumor. (1978) (2)
- Ketotifen and Neurofibromatosis-Reply (1988) (1)
- Premature centromere division. (1983) (1)
- A Geneticist's Approach to Deafness. (1979) (1)
- Neurofibromatosis: A Spectrum of Disorders (1989) (1)
- Deletion of 11q: report of two cases and a review. (1976) (1)
- Cancer surveys: Advances and prospects in clinical, epidemiological and laboratory oncology. Vol. 9, nos. 3 and 4: Genetics and cancer, parts 1 and 2 (1992) (1)
- Von Recklinghausen neurofibromatosis: new perspectives. (1982) (1)
- Neurogenetics and the neurosurgeon. (1991) (0)
- The Praxitype: An Improved Interpretation of Genotype-Phenotype Variation (2019) (0)
- Editorial: New educational initiative for the journal. (1987) (0)
- Heterogeneity andsuperficial X-linkage mimicry (1977) (0)
- NF is more than neurofibromas. (1988) (0)
- Head circumference and anthropometric changes and their relation to plexiform and skin neurofibromas in sporadic and familial neurofibromatosis 1 Brazilian adults: a cross-sectional study (2022) (0)
- Genetic issues in public health and medicine, B.H. Cohen, A.M. Lilienfeld and P.C. Huang (editors), Charles C. Thomas, Springfield, Illinois, 1978, 486 pages, $27.00 (1978) (0)
- Commentary Neurofibromatosis and Related Tumors Natural Occurrence and Animal Models (2007) (0)
- Chromosome Translocations inCouples withMultiple Spontaneous Abortions (1982) (0)
- Two-step mutation theory for retinoblastoma: Ultrastructural support (1980) (0)
- Growth curves for height and head circumference. (2000) (0)
- Erratum (1976) (0)
- News Briefs (1954) (0)
- Genotype–phenotype correlations in the genomic age: Concordance in monozygous twin pairs (2011) (0)
- Trisomy 8. (1974) (0)
- Title The path forward : 2015 International Children ' s Tumor Foundation conference on neurofibromatosis type 1 , type 2 , and schwannomatosis Permalink (2017) (0)
- Multiplicity as a Factor in Understanding NF1 (2018) (0)
- Clinical manifestations of NF1 in African-Americans and Caucasians (2000) (0)
- Announcements and news (2005) (0)
- DELETED Y CHROMOSOME (1968) (0)
- Nonverbal communication as an element of genetic counseling. (1979) (0)
- NF 1 and the Praxitype (2016) (0)
- Guidelines for organizing a comprehensive neurofibromatosis program. (1988) (0)
- Regional genetic counseling. In local health care. (1974) (0)
- Neurofibromatosis 1 Somatic Mutation Triggering Cellular Apoptosis to Prevent Neurofibromatosis 1 Progression (2020) (0)
- Pathology Hiding in Plain Sight: The NF1 Plasma Membrane (2020) (0)
- Genetic Counseling asPartofHospital Care (1978) (0)
- Prader-Willi syndrome (1982) (0)
- Hands down: Reflecting on the 50th anniversary of the description of Trisomy 21 (2009) (0)
- Penetrance ofvon Recklinghausen Neurofibromatosis: A Distinction betweenPredecessors andDescendants (1988) (0)
- Conflict within the "community" of human malformation syndromes. (1977) (0)
- Modern medicine; modern consumerism. (1998) (0)
- Progressive disorders and associated complications (2013) (0)
- Bilateral second toe superposition associated with neurofibromatosis type 1 and NF1 whole gene deletion (2017) (0)
- Trisomy 8 mosaicism in the skin of a patient with leukemia. (1976) (0)
- Correction: Error in Abstract (1977) (0)
- A Clinicopathologic Study on the Role of Estrogen, Progesterone, and Their Classical and Nonclassical Receptors in Cutaneous Neurofibromas of Individuals With Neurofibromatosis 1. (2020) (0)
- Neurofibromatosis Type 1 (2009) (0)
- NF 1 Clinical Elements and The NF 1 Neurofibroma Burden (2016) (0)
- Editorial: Neurogenetics and the Neurosurgeon (1991) (0)
- The 1989 George Krejci memorial Award. (1989) (0)
- Response to letter to editor by doctors Fontaine and Vankemmel (1978) (0)
- Letters and comments. "Deleted Y chromosome". (1968) (0)
- Letter: Late sequelae of aberrant intrauterine bands. (1974) (0)
- Routine cranial neuroimaging of patients with or at risk for neurofibromatosis. (1988) (0)
- Military ethics and G-6-PD deficiency. (1972) (0)
- Is NF-1 always distinct from NF-2? (1989) (0)
- Multisystem burden of neurofibromatosis 1 in Denmark: registry- and population-based rates of hospitalizations over the life span (2020) (0)
- TISSUE CULTURE EXPERIMENTS IN HEREDITARY SKIN CANCER: DNA REPAIR SYNTHESIS. (1970) (0)
- Lifeline: Helical and historical (2003) (0)
- The neurofibromatosis: which one and why? (2014) (0)
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