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Meta-analysis of hepatic cytochrome P450 ontogeny to underwrite the prediction of pediatric pharmacokinetics using physiologically based pharmacokinetic modeling

Journal of clinical pharmacology, 2016-03, Vol.56 (3), p.266-283

2016

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Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.32-q25.3

Genes chromosomes & cancer, 2007-03, Vol.46 (3), p.302-309

2007

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Risk of tuberculosis in a large sample of patients with coeliac disease – a nationwide cohort study

Alimentary pharmacology & therapeutics, 2011-03, Vol.33 (6), p.689-696

2011

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Oral Delivery of 1,3‐Dicyclohexylurea Nanosuspension Enhances Exposure and Lowers Blood Pressure in Hypertensive Rats

Basic & clinical pharmacology & toxicology, 2008-05, Vol.102 (5), p.453-458

2008

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Development and Evaluation of Ontogeny Functions of the Major UDP‐Glucuronosyltransferase Enzymes to Underwrite Physiologically Based Pharmacokinetic Modeling in Pediatric Populations

Journal of clinical pharmacology, 2024-10, Vol.64 (10), p.1222-1235

2024

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Prenatal diagnosis now and in the future, in a genetic perspective

Acta obstetricia et gynecologica Scandinavica, 2000, Vol.79 (11), p.925-927

Wahlström, Jan

2000

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Chromosomes in Anorexia Nervosa. A Study of 47 Cases Including a Population-Based Group: A Research Note

Journal of child psychology and psychiatry, 1991-05, Vol.32 (4), p.695-701

1991

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A population genetic study of psoriasis

British journal of dermatology (1951), 1994-07, Vol.131 (1), p.32-39

1994

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PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families

Human mutation, 2000-11, Vol.16 (5), p.395-400

2000

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Leber's hereditary optic neuropathy and complex I deficiency in muscle

Annals of neurology, 1991-11, Vol.30 (5), p.701-708

1991

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T cell repertoire in patients with multiple myeloma and monoclonal gammopathy of undetermined significance: Clonal CD8+ T cell expansions are found preferentially in patients with a low tumor burden

European journal of immunology, 1997-09, Vol.27 (9), p.2245-2252

1997

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Restricted T cell receptor BV gene usage in the lungs and muscles of patients with idiopathic inflammatory myopathies

Arthritis and rheumatism, 2007-01, Vol.56 (1), p.372-383

2007

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Prenatal diagnosis now and in the future, in a genetic perspective

Acta obstetricia et gynecologica Scandinavica, 2000-11, Vol.79 (11), p.925-927

WAHLSTRÖM, JAN

2000

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Preimplantation genetic diagnosis (PGD): The Gothenburg experience

Acta obstetricia et gynecologica Scandinavica, 2001-04, Vol.80 (4), p.331-336

2001

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Rett syndrome: random X chromosome inactivation

Clinical genetics, 1994-05, Vol.45 (5), p.274-275

1994

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CHROMOSOME ABNORMALITIES IN INFANTILE AUTISM AND OTHER CHILDHOOD PSYCHOSES: A POPULATION STUDY OF 66 CASES

Developmental medicine and child neurology, 1985-06, Vol.27 (3), p.293-304

1985

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Prenatal diagnosis now and in the future, in a genetic perspective

Acta obstetricia et gynecologica Scandinavica, 2000-11, Vol.79 (11), p.925-927

Wahlstrom, Jan

2000

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CONGENITAL MALFORMATIONS AND MATERNAL CONSUMPTION OF BENZODIAZEPINES: A CASE‐CONTROL STUDY

Developmental medicine and child neurology, 1990-05, Vol.32 (5), p.432-441

1990

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Preimplantation genetic diagnosis (PGD): The Gothenburg experience

Acta obstetricia et gynecologica Scandinavica, 2001, Vol.80 (4), p.331-331

2001

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Rett syndrome: potential gene sources - phenotypical variability

Clinical genetics, 1995-10, Vol.48 (4), p.169-172

1995

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Infantile autism and the fragile X. A swedish multicenter study

American journal of medical genetics, 1986-01, Vol.23 (1-2), p.403-408

1986

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TEENAGE PSYCHOSES-EPIDEMIOLOGY, CLASSIFICATION AND REDUCED OPTIMALITY IN THE PRE-, PERI-AND NEONATAL PERIODS

Journal of child psychology and psychiatry, 1986-01, Vol.27 (1), p.87-98

1986

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The Syndromes Described by Kanner and Rett‐Hagberg: Overlap in an Extended Family

Developmental medicine and child neurology, 1990-03, Vol.32 (3), p.258-261

1990

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Frequency of the fragile X syndrome in infantile autism

Clinical genetics, 1985-02, Vol.27 (2), p.113-117

1985

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Allergen-Specific MHC Class II Tetramer super(+) Cells Are Detectable in Allergic, but Not in Nonallergic, Individuals

Journal of Immunology, 2006-04, Vol.176 (8), p.5069-5077

2006

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Meta-analysis of hepatic cytochrome P450 ontogeny to underwrite the prediction of pediatric pharmacokinetics using physiologically based pharmacokinetic modeling

Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.32-q25.3

Risk of tuberculosis in a large sample of patients with coeliac disease – a nationwide cohort study

Oral Delivery of 1,3‐Dicyclohexylurea Nanosuspension Enhances Exposure and Lowers Blood Pressure in Hypertensive Rats

Development and Evaluation of Ontogeny Functions of the Major UDP‐Glucuronosyltransferase Enzymes to Underwrite Physiologically Based Pharmacokinetic Modeling in Pediatric Populations

Prenatal diagnosis now and in the future, in a genetic perspective

Chromosomes in Anorexia Nervosa. A Study of 47 Cases Including a Population-Based Group: A Research Note

A population genetic study of psoriasis

PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families

Leber's hereditary optic neuropathy and complex I deficiency in muscle

T cell repertoire in patients with multiple myeloma and monoclonal gammopathy of undetermined significance: Clonal CD8+ T cell expansions are found preferentially in patients with a low tumor burden

Restricted T cell receptor BV gene usage in the lungs and muscles of patients with idiopathic inflammatory myopathies

Prenatal diagnosis now and in the future, in a genetic perspective

Preimplantation genetic diagnosis (PGD): The Gothenburg experience

Rett syndrome: random X chromosome inactivation

CHROMOSOME ABNORMALITIES IN INFANTILE AUTISM AND OTHER CHILDHOOD PSYCHOSES: A POPULATION STUDY OF 66 CASES

Prenatal diagnosis now and in the future, in a genetic perspective

CONGENITAL MALFORMATIONS AND MATERNAL CONSUMPTION OF BENZODIAZEPINES: A CASE‐CONTROL STUDY

Preimplantation genetic diagnosis (PGD): The Gothenburg experience

Rett syndrome: potential gene sources - phenotypical variability

Infantile autism and the fragile X. A swedish multicenter study

TEENAGE PSYCHOSES-EPIDEMIOLOGY, CLASSIFICATION AND REDUCED OPTIMALITY IN THE PRE-, PERI-AND NEONATAL PERIODS

The Syndromes Described by Kanner and Rett‐Hagberg: Overlap in an Extended Family

Frequency of the fragile X syndrome in infantile autism

Allergen-Specific MHC Class II Tetramer super(+) Cells Are Detectable in Allergic, but Not in Nonallergic, Individuals

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