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Precision medicine for suicidality: from universality to subtypes and personalization

Molecular psychiatry, 2017-09, Vol.22 (9), p.1250-1273

2017

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Understanding and predicting suicidality using a combined genomic and clinical risk assessment approach

Molecular psychiatry, 2015-11, Vol.20 (11), p.1266-1285

2015

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Gene Expression in Biopsies of Acute Rejection and Interstitial Fibrosis/Tubular Atrophy Reveals Highly Shared Mechanisms That Correlate With Worse Long‐Term Outcomes

American journal of transplantation, 2016-07, Vol.16 (7), p.1982-1998

2016

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Towards understanding and predicting suicidality in women: biomarkers and clinical risk assessment

Molecular psychiatry, 2016-06, Vol.21 (6), p.768-785

2016

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Orthogonal Comparison of Molecular Signatures of Kidney Transplants With Subclinical and Clinical Acute Rejection: Equivalent Performance Is Agnostic to Both Technology and Platform

American journal of transplantation, 2017-08, Vol.17 (8), p.2103-2116

2017

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Molecular Classifiers for Acute Kidney Transplant Rejection in Peripheral Blood by Whole Genome Gene Expression Profiling

American journal of transplantation, 2014-05, Vol.14 (5), p.1164-1172

2014

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The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic

Annals of internal medicine, 2000-09, Vol.133 (5), p.329

2000

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Hemolytic anemia associated with a novel heterozygote mutation 1183A in the PK-LR gene (PK- Jordan)

International journal of laboratory hematology, 2014-08, Vol.36 (4), p.e66-e68

2014

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THU0315 A Study of Gene Expression in Fibromyalgia: An Analysis of Potential Biological Markers

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.309-309

2015

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Genetics of iron storage and hemochromatosis

Drug metabolism and disposition, 2001-04, Vol.29 (4 Pt 2), p.495

2001

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Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to gamma-glutamylcysteine synthetase deficiency in a patient of Moroccan origin

Haematologica (Roma), 2007-11, Vol.92 (11), p.e102-e105

2007

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Synergy between TLR2 and TLR4: A safety mechanism

Blood cells, molecules, & diseases, 2001-07, Vol.27 (4), p.728-730

2001

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Regulation of Hepcidin Transcription by Interleukin-1 and Interleukin-6

Proceedings of the National Academy of Sciences - PNAS, 2005-02, Vol.102 (6), p.1906-1910

2005

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The molecular basis of a case of γ-glutamylcysteine synthetase deficiency

Blood, 1999-10, Vol.94 (8), p.2890-2894

1999

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Hematologically Important Mutations: Gaucher Disease

Blood cells, molecules, & diseases, 1998-03, Vol.24 (1), p.2-8

1998

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Interference of heparin with the polymerase chain reaction

BioTechniques, 1990-08, Vol.9 (2), p.166

1990

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Racial Variability in the UDP-Glucuronosyltransferase 1 (UGT1A1) Promoter: A Balanced Polymorphism for Regulation of Bilirubin Metabolism?

Proceedings of the National Academy of Sciences - PNAS, 1998-07, Vol.95 (14), p.8170-8174

1998

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Gaucher disease : gene frequencies in the Ashkenazi Jewish population

American journal of human genetics, 1993, Vol.52 (1), p.85-88

1993

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Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA

The Lancet (British edition), 2002-01, Vol.359 (9302), p.211-218

2002

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Identification of the Second Common Jewish Gaucher Disease Mutation Makes Possible Population-Based Screening for the Heterozygous State

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (23), p.10544-10547

1991

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A previously undescribed nonsense mutation of the HFE gene

Clinical genetics, 2002-01, Vol.61 (1), p.40-42

2002

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Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to {gamma}-glutamylcysteine synthetase deficiency in a patient of Moroccan origin

Haematologica (Roma), 2007-11, Vol.92 (11), p.e102-e105

2007

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Coinheritance of Alleles Associated With Hemochromatosis and Hereditary Hyperferritinemia-Cataract Syndrome

Blood, 1998-12, Vol.92 (11), p.4480-4481

1998

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Hematologically important mutations: Gaucher disease

Blood cells, molecules, & diseases, 2005-11, Vol.35 (3), p.355-364

2005

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Genome-wide expression profiling in the peripheral blood of patients with fibromyalgia

Clinical and experimental rheumatology, 2016-03, Vol.34 (2 Suppl 96), p.S89

2016

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Precision medicine for suicidality: from universality to subtypes and personalization

Understanding and predicting suicidality using a combined genomic and clinical risk assessment approach

Gene Expression in Biopsies of Acute Rejection and Interstitial Fibrosis/Tubular Atrophy Reveals Highly Shared Mechanisms That Correlate With Worse Long‐Term Outcomes

Towards understanding and predicting suicidality in women: biomarkers and clinical risk assessment

Orthogonal Comparison of Molecular Signatures of Kidney Transplants With Subclinical and Clinical Acute Rejection: Equivalent Performance Is Agnostic to Both Technology and Platform

Molecular Classifiers for Acute Kidney Transplant Rejection in Peripheral Blood by Whole Genome Gene Expression Profiling

The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic

Hemolytic anemia associated with a novel heterozygote mutation 1183A in the PK-LR gene (PK- Jordan)

THU0315 A Study of Gene Expression in Fibromyalgia: An Analysis of Potential Biological Markers

Genetics of iron storage and hemochromatosis

Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to gamma-glutamylcysteine synthetase deficiency in a patient of Moroccan origin

Synergy between TLR2 and TLR4: A safety mechanism

Regulation of Hepcidin Transcription by Interleukin-1 and Interleukin-6

The molecular basis of a case of γ-glutamylcysteine synthetase deficiency

Hematologically Important Mutations: Gaucher Disease

Interference of heparin with the polymerase chain reaction

Racial Variability in the UDP-Glucuronosyltransferase 1 (UGT1A1) Promoter: A Balanced Polymorphism for Regulation of Bilirubin Metabolism?

Gaucher disease : gene frequencies in the Ashkenazi Jewish population

Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA

Identification of the Second Common Jewish Gaucher Disease Mutation Makes Possible Population-Based Screening for the Heterozygous State

A previously undescribed nonsense mutation of the HFE gene

Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to {gamma}-glutamylcysteine synthetase deficiency in a patient of Moroccan origin

Coinheritance of Alleles Associated With Hemochromatosis and Hereditary Hyperferritinemia-Cataract Syndrome

Hematologically important mutations: Gaucher disease

Genome-wide expression profiling in the peripheral blood of patients with fibromyalgia

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