Suchergebnisse

PubPharm (15.958)

51

Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat allele

enthalten in: Annals of human genetics | 2024

von Baum, L. | Lee, C. | Ye, R. | +8

52

Chronic Obstructive Pulmonary Disease and Osteoporosis : A Two-Sample Mendelian Randomization Analysis

enthalten in: Chronic obstructive pulmonary diseases (Miami, Fla.) | 2024

von Dou, Z. | Chen, X. | Chen, J. | +2

53

Genetic and multi-omic risk assessment of Alzheimer's disease implicates core associated biological domains

enthalten in: Alzheimer's & dementia (New York, N. Y.) | 2024

von Cary, G. | Wiley, J. | Gockley, J. | +10

54

Familial genetic and environmental transmission of depression : A multi-informant twin family study

enthalten in: PsyCh journal | 2024

von Ding, Q. | Zhou, Y. | Yu, S. | +3

55

Supravalvular Aortic Stenosis in Homozygous Familial Hypercholesterolemia : Contemporary Management

enthalten in: JACC. Case reports | 2024

von Eisenberg, S. | Gold, D. | Mehta, P. | +2

56

Public preferences for pharmacogenetic testing in the NHS : Embedding a discrete choice experiment within service design to better meet user needs

enthalten in: British journal of clinical pharmacology | 2024

von McDermott, J. | Sharma, V. | Newman, W. | +3

57

Neurological, cardiac, musculoskeletal, and renal manifestations of scleroderma along with insights into its genetics, pathophysiology, diagnostic, and therapeutic updates

enthalten in: Health science reports | 2024

von Prajjwal, P. | Marsool, M. | Yadav, V. | +12

58

Familial Chiari malformation : a systematic review and illustrative cases

enthalten in: Journal of neurosurgery. Spine | 2024

von Dhawan, A. | Dhawan, J. | Sharma, A. | +3

59

Genetics may affect the risk of undergoing surgery for rhizarthrosis

enthalten in: Journal of orthopaedic research : official publication of the Orthopaedic Research Society | 2024

von Henkel, C. | DBDS Genomic Consortium | Erikstrup, C. | +3

60

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel

enthalten in: European journal of haematology | 2024

von Yeshareem, L. | Yacobovich, J. | Lebel, A. | +26