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Ying Liu; Kyriakie Sarafoglou; Kristi Bentler; Juliet S Chhay; Bradford Coffee; Judith L Fridovich-Keil
A Case Study of Monozygotic Twins Apparently Homozygous for a Novel Variant of UDP-Galactose 4'-epimerase (GALE) : A Complex Case of Variant GALE.
Meghan E Quirk; Bradford Coffee; Steven F Dobrowolski; Benjamin E Nelson; Rani H Singh
Utility of phenylalanine hydroxylase genotype for tetrahydrobiopterin responsiveness classification in patients with phenylketonuria.
S Hussain Askree; Shika Dharamrup; Lawrence N Hjelm; Bradford Coffee
Parent-of-origin testing for 15q11-q13 gains by quantitative DNA methylation analysis.

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2013: Ying Liu; Kyriakie Sarafoglou; Kristi Bentler; Juliet S Chhay; Bradford Coffee; Judith L Fridovich-Keil
A Case Study of Monozygotic Twins Apparently Homozygous for a Novel Variant of UDP-Galactose 4'-epimerase (GALE) : A Complex Case of Variant GALE.
JIMD reports 2013;7():89-98.
2012: Meghan E Quirk; Bradford Coffee; Steven F Dobrowolski; Benjamin E Nelson; Rani H Singh
Utility of phenylalanine hydroxylase genotype for tetrahydrobiopterin responsiveness classification in patients with phenylketonuria.
Molecular genetics and metabolism 2012;107(1-2):31-6.
2012: S Hussain Askree; Shika Dharamrup; Lawrence N Hjelm; Bradford Coffee
Parent-of-origin testing for 15q11-q13 gains by quantitative DNA methylation analysis.
The Journal of molecular diagnostics : JMD 2012;14(3):192-8.
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: Stephen C Collins; Steven M Bray; Joshua A Suhl; David J Cutler; Bradford Coffee; Zwick Michael; Stephen Warren
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males.
American journal of medical genetics. Part A 2010;152A(10):2512-20.
2010: Bradford Coffee
Commentary on population screening for fragile X syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics 2010;12(7):411-2.
2009: Bradford Coffee; Krayton Keith; Igor Albizua; Tamika Malone; Julie Mowrey; Stephanie L Sherman; Stephen Warren
Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.
American journal of human genetics 2009;85(4):503-14.
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: Bradford Coffee; Morna Ikeda; DEJAN BUDIMIROVIC; Lawrence N Hjelm; Walter E Kaufmann; Stephen Warren
Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature.
American journal of medical genetics. Part A 2008;146A(10):1358-67.
2006: Bradford Coffee; Lawrence N Hjelm; Angela DeLorenzo; Ebony M Courtney; Chunli Yu; Kasinathan Muralidharan
Characterization of an unusual deletion of the galactose-1-phosphate uridyl transferase (GALT) gene.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(10):635-40.
2006: Bradford Coffee; Kasinathan Muralidharan; W Edward Highsmith; Pablo Lapunzina; Stephen Warren
Molecular diagnosis of Beckwith-Wiedemann syndrome using quantitative methylation-sensitive polymerase chain reaction.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(10):628-34.
2004: Karen Smith; Bradford Coffee; Daniel Reines
Occupancy and synergistic activation of the FMR1 promoter by Nrf-1 and Sp1 in vivo.
Human molecular genetics 2004;13(15):1611-21.
2002: Bradford Coffee; Fuping Zhang; Stephanie Ceman; Stephen Warren; Daniel Reines
Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome.
American journal of human genetics 2002;71(4):923-32.
1999: Bradford Coffee; Fuping Zhang; Stephen Warren; Daniel Reines
Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.
Nature genetics 1999;22(1):98-101.