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Genome-wide association study indicates two novel resistance loci for severe malaria

Nature (London), 2012-09, Vol.489 (7416), p.443-446

2012

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Genetic predisposition ( NLRP3 V198M mutation) for IL-1–mediated inflammation in a patient with Schnitzler syndrome

Journal of allergy and clinical immunology, 2010-02, Vol.125 (2), p.500-502

2010

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Lack of Association of CD55 Receptor Genetic Variants and Severe Malaria in Ghanaian Children

G3 : genes - genomes - genetics, 2017-03, Vol.7 (3), p.859-864

2017

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Genome-wide linkage analysis of malaria infection intensity and mild disease

PLoS genetics, 2007-03, Vol.3 (3), p.e48-e48

2007

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A -436C>A polymorphism in the human FAS gene promoter associated with severe childhood malaria

PLoS genetics, 2011-05, Vol.7 (5), p.e1002066-e1002066

2011

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Reply to Pandey

The Journal of infectious diseases, 2009-01, Vol.199 (2), p.286-287

Timmann, Christian

2009

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Colchicine use in children and adolescents with familial Mediterranean fever: literature review and consensus statement

Pediatrics (Evanston), 2007-02, Vol.119 (2), p.e474

2007

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The Prevalence of Sickle Cell Disease and Its Implication for Newborn Screening in Germany (Hamburg Metropolitan Area)

Pediatric blood & cancer, 2016-01, Vol.63 (1), p.168-170

2016

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Genotyping of Plasmodium falciparum Pyrimethamine Resistance by Matrix-Assisted Laser Desorption-Ionization Time-of-Flight Mass Spectrometry

Antimicrobial Agents and Chemotherapy, 2004-02, Vol.48 (2), p.466-472

2004

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Hemoglobin variants and disease manifestations in severe falciparum malaria

JAMA : the journal of the American Medical Association, 2007-05, Vol.297 (20), p.2220

2007

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Malaria, mummies, mutations: Tutankhamun’s archaeological autopsy: Tutankhamun’s cause of death

Tropical medicine & international health, 2010-11, Vol.15 (11), p.1278-1280

2010

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Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics

Rheumatology (Oxford, England), 2009-08, Vol.48 (8), p.987-991

2009

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King Tutankhamun's family and demise

JAMA : the journal of the American Medical Association, 2010-06, Vol.303 (24), p.2473; author reply 2473

2010

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Malaria, mummies, mutations: Tutankhamun's archaeological autopsy

Tropical medicine & international health, 2010-11, Vol.15 (11), p.1278-1280

2010

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The spectrum of β-thalassemia mutations in Gaza Strip, Palestine

Blood cells, molecules, & diseases, 2013-04, Vol.50 (4), p.247-251

2013

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CCN1 Mutation is Associated with Atrial Septal Defect

Pediatric cardiology, 2015-02, Vol.36 (2), p.295-299

2015

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FCGR2A functional genetic variant associated with susceptibility to severe malarial anaemia in Ghanaian children

Journal of medical genetics, 2010-07, Vol.47 (7), p.471-475

2010

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Hereditary Periodic Fever With Systemic Amyloidosis: Is Hyper-IgD Syndrome Really a Benign Disease?

American journal of kidney diseases, 2006-09, Vol.48 (3), p.e41-e45

2006

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Disentangling malaria anaemia

Malaria journal, 2014-09, Vol.13 (S1), p.O21-O21, Article O21

2014

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Capillary refill time as an independent prognostic indicator in severe and complicated malaria

The Journal of pediatrics, 2006-11, Vol.149 (5), p.676-681

2006

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Human Genetic Resistance to Onchocerca volvulus: Evidence for Linkage to Chromosome 2p from an Autosome-Wide Scan

The Journal of infectious diseases, 2008-08, Vol.198 (3), p.427-433

2008

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Selection for deafness?

Nature medicine, 2002-12, Vol.8 (12), p.1332-1333

2002

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A -436CA polymorphism in the human FAS gene promoter associated with severe childhood malaria

PLoS genetics, 2011-05, Vol.7 (5)

2011

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A -436C>A Polymorphism in the Human FAS Gene Promoter Associated with Severe Childhood Malaria: e1002066

PLoS genetics, 2011-05, Vol.7 (5)

2011

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The new Powerplex® ESX17 and ESI17 kits in paternity and maternity analyses involving people from Africa—including allele frequencies for three African populations

International journal of legal medicine, 2011, Vol.125 (1), p.149-154

2011

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Genome-wide association study indicates two novel resistance loci for severe malaria

Genetic predisposition ( NLRP3 V198M mutation) for IL-1–mediated inflammation in a patient with Schnitzler syndrome

Lack of Association of CD55 Receptor Genetic Variants and Severe Malaria in Ghanaian Children

Genome-wide linkage analysis of malaria infection intensity and mild disease

A -436C>A polymorphism in the human FAS gene promoter associated with severe childhood malaria

Reply to Pandey

Colchicine use in children and adolescents with familial Mediterranean fever: literature review and consensus statement

The Prevalence of Sickle Cell Disease and Its Implication for Newborn Screening in Germany (Hamburg Metropolitan Area)

Genotyping of Plasmodium falciparum Pyrimethamine Resistance by Matrix-Assisted Laser Desorption-Ionization Time-of-Flight Mass Spectrometry

Hemoglobin variants and disease manifestations in severe falciparum malaria

Malaria, mummies, mutations: Tutankhamun’s archaeological autopsy: Tutankhamun’s cause of death

Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics

King Tutankhamun's family and demise

Malaria, mummies, mutations: Tutankhamun's archaeological autopsy

The spectrum of β-thalassemia mutations in Gaza Strip, Palestine

CCN1 Mutation is Associated with Atrial Septal Defect

FCGR2A functional genetic variant associated with susceptibility to severe malarial anaemia in Ghanaian children

Hereditary Periodic Fever With Systemic Amyloidosis: Is Hyper-IgD Syndrome Really a Benign Disease?

Disentangling malaria anaemia

Capillary refill time as an independent prognostic indicator in severe and complicated malaria

Human Genetic Resistance to Onchocerca volvulus: Evidence for Linkage to Chromosome 2p from an Autosome-Wide Scan

Selection for deafness?

A -436CA polymorphism in the human FAS gene promoter associated with severe childhood malaria

A -436C>A Polymorphism in the Human FAS Gene Promoter Associated with Severe Childhood Malaria: e1002066

The new Powerplex® ESX17 and ESI17 kits in paternity and maternity analyses involving people from Africa—including allele frequencies for three African populations

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