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3. Why the spaces in which we deliver care matter: implications and recommendations for general practice.

4. BKCachannels are involved in spontaneous and lipopolysaccharide-stimulated uterine contraction in late gestation mice†

5. High Loading of Polygenic Risk for ADHD in Children With Comorbid Aggression

7. Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3

8. Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD

9. CITED2 is a conserved regulator of the uterine–placental interface

11. Dosage-dependent copy number gains in E2f1 and E2f3 drive hepatocellular carcinoma

13. CITED2 is a Conserved Regulator of the Uterine-Placental Interface

15. E2f8 mediates tumor suppression in postnatal liver development

16. Imaging Mass Spectrometry Reveals Alterations in N-Linked Glycosylation That Are Associated With Histopathological Changes in Nonalcoholic Steatohepatitis in Mouse and Human

17. Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

18. Insights into the Control of Attentional Set in ADHD Using the Attentional Blink Paradigm

21. Fetal Abuse.

22. On the role of NOS1 ex1f-VNTR in ADHD—allelic, subgroup, and meta-analysis

23. Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

24. Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder

26. Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder (Nature Communications, (2021), 12, 1, (576), 10.1038/s41467-020-20443-2)

27. Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

28. A rare missense variant in theATP2C2gene is associated with language impairment and related measures

30. A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures

31. Maintenance of Treatment Effects

32. Motivation

33. Monotonic Voice

34. Memory Development

35. Movement Assessment Battery for Children: 2nd Edition (MABC-2)

36. Manual Sign

37. μ Rhythm

38. Minimal Brain Dysfunction

39. MABC-2

40. More Than Words

41. Metachromatic Leukodystrophy

42. Multilocus Genetic Models

43. Mutual Gaze

44. Multiple Complex (or Multiplex) Developmental Disorder

45. Mental Retardation

46. Motor Development Assessment

47. Massive Infantile Spasms

48. Marketed as Geodon

49. Male Turner

50. Miller Function and Participation Scales

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