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List of works by Gerald Raymond

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

scientific article published in June 2010

Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations

scientific article

Auditory function in adrenomyeloneuropathy

scientific article

BMP4 was associated with NSCL/P in an Asian population

scientific article

Cerebrospinal fluid matrix metalloproteinases are elevated in cerebral adrenoleukodystrophy and correlate with MRI severity and neurologic dysfunction

scientific article

Childhood Cerebral Adrenoleukodystrophy: MR Perfusion Measurements and Their Use in Predicting Clinical Outcome after Hematopoietic Stem Cell Transplantation.

scientific article published on 14 April 2016

Chitotriosidase as a biomarker of cerebral adrenoleukodystrophy

scientific article published on 20 October 2011

Combined extraction of acyl carnitines and 26:0 lysophosphatidylcholine from dried blood spots: prospective newborn screening for X-linked adrenoleukodystrophy

scientific article

Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders

scientific article

Elevated cerebral spinal fluid cytokine levels in boys with cerebral adrenoleukodystrophy correlates with MRI severity

scientific article

Follow-up of 89 asymptomatic patients with adrenoleukodystrophy treated with Lorenzo's oil.

scientific article

Intensity of MRI Gadolinium Enhancement in Cerebral Adrenoleukodystrophy: A Biomarker for Inflammation and Predictor of Outcome following Transplantation in Higher Risk Patients

scientific article published on October 2015

Long-term outcomes after allogeneic hematopoietic stem cell transplantation for metachromatic leukodystrophy: the largest single-institution cohort report.

scientific article

Multi-institutional assessments of transplantation for metabolic disorders

scientific article

Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly

scientific article

Peroxisome biogenesis disorders

scientific article

The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder

scientific article

X-linked adrenoleukodystrophy.

scientific article

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