Suchergebnisse

PubPharm (15.958)

21

A de novo pathogenic variant in MICAL-1 causes epilepsy with auditory features

enthalten in: Epilepsia open | 2024

von Bonanni, P. | Giorda, R. | Michelucci, R. | +2

22

Identifying atopic dermatitis risk loci in 1,094,060 individuals with sub analysis of disease severity and onset

enthalten in: The Journal of investigative dermatology | 2024

von Pasanen, A. | Sliz, E. | Huilaja, L. | +7

23

Multiple enchondromas and hobnail hemangiomas revealing a rare type of Maffucci syndrome

enthalten in: International journal of dermatology | 2024

von Tzoumpa, S. | Nuñez, J. | Postigo-Mac Dowall, M. | +2

24

Convergent epigenetic evolution drives relapse in acute myeloid leukemia

enthalten in: eLife | 2024

von Nuno, K. | Azizi, A. | Koehnke, T. | +5

UpdateOf: bioRxiv. 2023 Oct 10;:. - PMID 37873452

25

Antipsychotic-induced epigenomic reorganization in frontal cortex of individuals with schizophrenia

enthalten in: eLife | 2024

von Zhu, B. | Ainsworth, R. | Wang, Z. | +8

26

Early identification of SOX17 deficiency in infants to guide management of heritable pulmonary arterial hypertension using PDA stent to create reverse Potts shunt physiology

enthalten in: Pulmonary circulation | 2024

von Ostler, H. | Fall, C. | El-Said, H. | +4

27

Characterization of the genetic determinants of context-specific DNA methylation in primary monocytes

enthalten in: Cell genomics | 2024

von Gilchrist, J. | Fang, H. | Danielli, S. | +13

28

APOE ε2-Carriers Are Associated with an Increased Risk of Primary Angle-Closure Glaucoma in Patients of Saudi Origin

enthalten in: International journal of molecular sciences | 2024

von Kondkar, A. | Azad, T. | Sultan, T. | +8

29

Views of Genetic Testing for Autism Among Autism Self-Advocates : A Qualitative Study

enthalten in: AJOB empirical bioethics | 2024

von Klitzman, R. | Bezborodko, E. | Chung, W. | +1

30

The construction of genetics teaching resources related to colour blindness and their application in genetics teaching

enthalten in: Yi chuan = Hereditas | 2024

von Chun-Xiao, M.