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Lora Bean

Research Profile

Disorders

Chemicals & Drugs

Genes & Molecular Sequences

Physiology

Phenomena

Phosphorylation

Procedures

Anatomy

Chromosomes, Human, Pair 21

Co-author Network

Publications

TOP 3
NaTasha D Hollis; Leslie A O'Leary; Tiffany Renee Oliver; Paul A Romitti; Marjorie H Royle; Stephanie L Sherman; Stuart W Tinker; Claudine P Torfs; Emily G Allen; Charlotte M Druschel; Sallie B Freeman; Charlotte A Hobbs; Lora J H Bean
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.
Christine Ackerman; Lora J H Bean; Clifford L Cua; Kenneth J Dooley; Karina Espana; Eleanor Feingold; Adam E Locke; Sean Mooney; Roger H Reeves; Benjamin Reshey; Stephanie L Sherman; Janita Thusberg; Cheryl L Maslen
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects.
Tiffany Renee Oliver; Stuart W Tinker; Emily G Allen; Lora J H Bean; Ferdouse Begum; Vivian Cheung; Reshmi Chowdhury; Eleanor Feingold; Natasha Hollis; Adam E Locke; Mary Marazita; Stephanie L Sherman
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

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All Publications

2013: NaTasha D Hollis; Leslie A O'Leary; Tiffany Renee Oliver; Paul A Romitti; Marjorie H Royle; Stephanie L Sherman; Stuart W Tinker; Claudine P Torfs; Emily G Allen; Charlotte M Druschel; Sallie B Freeman; Charlotte A Hobbs; Lora J H Bean
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.
American journal of medical genetics. Part A 2013;161(3):438-44.
2012: Christine Ackerman; Lora J H Bean; Clifford L Cua; Kenneth J Dooley; Karina Espana; Eleanor Feingold; Adam E Locke; Sean Mooney; Roger H Reeves; Benjamin Reshey; Stephanie L Sherman; Janita Thusberg; Cheryl L Maslen
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects.
American journal of human genetics 2012;91(4):646-59.
2012: Tiffany Renee Oliver; Stuart W Tinker; Emily G Allen; Lora J H Bean; Ferdouse Begum; Vivian Cheung; Reshmi Chowdhury; Eleanor Feingold; Natasha Hollis; Adam E Locke; Mary Marazita; Stephanie L Sherman
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.
Human genetics 2012;131(7):1039-46.
2011: Patrick Yu-Wai-Man; Suma P Shankar; Valérie Biousse; Neil R Miller; Lora J H Bean; Bradford Coffee; Madhuri Hegde; Nancy J Newman
Genetic screening for OPA1 and OPA3 mutations in patients with suspected inherited optic neuropathies.
Ophthalmology 2011;118(3):558-63.
2011: Syed Hussain Askree; Lawrence N Hjelm; Muhammad Ali Pervaiz; Margaret Adam; Lora J H Bean; Madhuri Hedge; Bradford Coffee
Allelic dropout can cause false-positive results for Prader-Willi and Angelman syndrome testing.
The Journal of molecular diagnostics : JMD 2011;13(1):108-12.
2010: Adam E Locke; Kenneth J Dooley; Stuart W Tinker; Soo Yeon Cheong; Eleanor Feingold; Emily G Allen; Sallie B Freeman; Claudine P Torfs; Clifford L Cua; Michael P Epstein; Michael C Wu; Xihong Lin; George T Capone; Stephanie L Sherman; Lora J H Bean
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.
Genetic epidemiology 2010;34(6):613-23.
2010: Lawrence N Hjelm; Ephrem L H Chin; Madhuri R Hegde; Bradford W Coffee; Lora J H Bean
A simple method to confirm and size deletion, duplication, and insertion mutations detected by sequence analysis.
The Journal of molecular diagnostics : JMD 2010;12(5):607-10.
2009: Amanda E Carney; Rebecca D Sanders; Kerry R Garza; Lee Anne McGaha; Lora J H Bean; Bradford W Coffee; James W Thomas; David J Cutler; Natalie L Kurtkaya; Judith L Fridovich-Keil
Origins, distribution and expression of the Duarte-2 (D2) allele of galactose-1-phosphate uridylyltransferase.
Human molecular genetics 2009;18(9):1624-32.
2009: Marwan K Tayeh; Ephrem Lip Hon Chin; Vanessa R Miller; Lora J H Bean; Bradford Coffee; Madhuri Hegde
Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications.
Genetics in medicine : official journal of the American College of Medical Genetics 2009;11(4):232-40.
2008: Yan Lin; Chien Cheng (George) Tseng; Soo Yeon Cheong; Lora J H Bean; Stephanie L Sherman; Eleanor Feingold
Smarter clustering methods for SNP genotype calling.
Bioinformatics (Oxford, England) 2008;24(23):2665-71.
2008: Margaret P Adam; April N Justice; Lora J H Bean; Paul M FERNHOFF
Mowat-Wilson syndrome with craniosynostosis: a case report.
American journal of medical genetics. Part A 2008;146A(2):245-6.
2006: Cheryl L Maslen; Darcie Babcock; Susan W Robinson; Lora J H Bean; Kenneth J Dooley; Virginia L Willour; Stephanie L Sherman
CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome.
American journal of medical genetics. Part A 2006;140(22):2501-5.
2004: Kimberly Kerstann; Eleanor Feingold; Sallie B Freeman; Lora J H Bean; Robert Pyatt; Stuart Tinker; Amy H Jewel; George T Capone; Stephanie L Sherman
Linkage disequilibrium mapping in trisomic populations: analytical approaches and an application to congenital heart defects in Down syndrome.
Genetic epidemiology 2004;27(3):240-51.
2002: Lora J H Bean; George R Stark
Regulation of the accumulation and function of p53 by phosphorylation of two residues within the domain that binds to Mdm2.
The Journal of biological chemistry 2002;277(3):1864-71.
2001: Mikhail V Chernov; Lora J H Bean; Natalia Lerner; George R Stark
Regulation of ubiquitination and degradation of p53 in unstressed cells through C-terminal phosphorylation.
The Journal of biological chemistry 2001;276(34):31819-24.
2001: Munna L Agarwal; chilakamarti ramana; M Hamilton; William R Taylor; S E DePrimo; Lora J H Bean; Ashok Agarwal; Mukesh K Agarwal; Alan Wolfman; George R Stark
Regulation of p53 expression by the RAS-MAP kinase pathway.
Oncogene 2001;20(20):2527-36.
2001: Lora J H Bean; George R Stark
Phosphorylation of serines 15 and 37 is necessary for efficient accumulation of p53 following irradiation with UV.
Oncogene 2001;20(9):1076-84.