PHILIP LUPO to Phenotype
This is a "connection" page, showing publications PHILIP LUPO has written about Phenotype.
Connection Strength
0.538
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Comprehensive assessment of the associations between maternal diabetes and structural birth defects in offspring: a phenome-wide association study. Ann Epidemiol. 2021 01; 53:14-20.e8.
Score: 0.085
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Schaaf-Yang syndrome overview: Report of 78 individuals. Am J Med Genet A. 2018 12; 176(12):2564-2574.
Score: 0.075
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Epidemiology of anophthalmia and microphthalmia: Prevalence and patterns in Texas, 1999-2009. Am J Med Genet A. 2018 09; 176(9):1810-1818.
Score: 0.074
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Family-based exome-wide assessment of maternal genetic effects on susceptibility to childhood B-cell acute lymphoblastic leukemia in hispanics. Cancer. 2016 Dec 01; 122(23):3697-3704.
Score: 0.064
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Spina bifida subtypes and sub-phenotypes by maternal race/ethnicity in the National Birth Defects Prevention Study. Am J Med Genet A. 2012 Jan; 158A(1):109-15.
Score: 0.046
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Polytomous logistic regression as a tool for exploring heterogeneity across birth defect subtypes: an example using anencephaly and spina bifida. Birth Defects Res A Clin Mol Teratol. 2010 Aug; 88(8):701-5.
Score: 0.042
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Common epilepsy variants from the general population are not associated with epilepsy among individuals with tuberous sclerosis complex. Am J Med Genet A. 2024 06; 194(6):e63569.
Score: 0.027
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Identification of USP9X as a leukemia susceptibility gene. Blood Adv. 2023 08 22; 7(16):4563-4575.
Score: 0.026
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Random field modeling of multi-trait multi-locus association for detecting methylation quantitative trait loci. Bioinformatics. 2022 08 10; 38(16):3853-3862.
Score: 0.024
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Tuberous Sclerosis Complex Genotypes and Developmental Phenotype. Pediatr Neurol. 2019 07; 96:58-63.
Score: 0.019
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Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies. Genet Med. 2019 08; 21(8):1797-1807.
Score: 0.019
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BRAF-V600E expression in precursor versus differentiated dendritic cells defines clinically distinct LCH risk groups. J Exp Med. 2014 Apr 07; 211(4):669-83.
Score: 0.014
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22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases. Pediatr Cardiol. 2013 Oct; 34(7):1687-94.
Score: 0.013
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Variants of folate metabolism genes and the risk of conotruncal cardiac defects. Circ Cardiovasc Genet. 2008 Dec; 1(2):126-32.
Score: 0.009