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1. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

3. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

4. Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism

5. A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans

9. Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth

10. Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine

11. Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms

12. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

14. Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood: Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits

15. Maternal Fiber Intake During Pregnancy and Development of Attention-Deficit/Hyperactivity Disorder Symptoms Across Childhood: The Norwegian Mother, Father, and Child Cohort Study

16. European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation

21. Author Correction: Characterization of the genetic architecture of infant and early childhood body mass index

22. The genetic architecture of sporadic and multiple consecutive miscarriage.

23. Molecular mechanism of HNF-1A–mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetes

24. Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration.

30. Functional characterization of HNF4A gene variants identify promoter and cell line specific transactivation effects

33. Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood:Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits

34. Ten Years of Improving Glycemic Control in Pediatric Diabetes Care: Data From the Norwegian Childhood Diabetes Registry.

35. Characterization of CEL-DUP2: Complete duplication of the carboxyl ester lipase gene is unlikely to influence risk of chronic pancreatitis

38. Congenital hyperinsulinism

40. Genome-wide analyses of vocabulary size in infancy and toddlerhood: associations with ADHD, literacy and cognition-related traits

41. Maternal Fiber Intake During Pregnancy and Development of Attention-Deficit/Hyperactivity Disorder Symptoms Across Childhood: The Norwegian Mother, Father, and Child Cohort Study

42. Impaired glucose tolerance and cardiovascular risk factors in relation to infertility: a Mendelian randomization analysis in the Norwegian Mother, Father, and Child Cohort Study

43. Parental Smoking and Risk of Childhood-onset Type 1 Diabetes

46. Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

47. Bioinformatics pipeline for the systematic mining genomic and proteomic variation linked to rare diseases: The example of monogenic diabetes.

48. Intrauterine Growth and Offspring Neurodevelopmental Traits: A Mendelian Randomization Analysis of the Norwegian Mother, Father and Child Cohort Study (MoBa).

49. Impaired glucose tolerance and cardiovascular risk factors in relation to infertility: a Mendelian randomization analysis in the Norwegian Mother, Father, and Child Cohort Study.

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