Search

Your search keyword '"Volk, Alexander"' showing total 447 results

Search Constraints

Start Over You searched for: Author "Volk, Alexander" Remove constraint Author: "Volk, Alexander"
447 results on '"Volk, Alexander"'

Search Results

1. The heterogeneous cancer phenotype of individuals with biallelic germline pathogenic variants in CHEK2

2. Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension

3. Modular Assembly of Metamaterials Using Light Gradients

4. Treatment outcome of atypical EGFR mutations in the German National Network Genomic Medicine Lung Cancer (nNGM)

6. Clinico-genetic findings in 509 frontotemporal dementia patients

10. A novel TTC26 variant in a patient with hexadactyly, pituitary stalk interruption, hepatopathy, nephropathy, and bilateral lip‐palate cleft: A case report and expansion of the phenotype.

12. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

18. Figure 1 from ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

19. Figure 3 from ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

20. Figure 6 from ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

21. Table S2 from ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

22. Data from ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

23. Figure 4 from ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

24. Supplementary Methods 1 from ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

25. Figure 2 from ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

26. Figure 5 from ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

27. Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients

31. The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy

32. Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor

33. ENIGMA CHEK2gether Project:A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

34. SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden

35. Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer

36. FDG-PET underscores the key role of the thalamus in frontotemporal lobar degeneration caused by C9ORF72 mutations

37. Poly‐GP in cerebrospinal fluid links C9orf72‐associated dipeptide repeat expression to the asymptomatic phase of ALS/FTD

38. Die autosomal dominant vererbte auditorische Neuropathie Typ 2 (AUNA2) wird verursacht durch eine Deletion im Gen für ATP11A

40. Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia withDAB1andC9ORF72Repeat Expansions: An 18‐Year Study

41. Disease modeling of a mutation in α‐actinin 2 guides clinical therapy in hypertrophic cardiomyopathy

42. Serum neurofilament light chain in behavioral variant frontotemporal dementia

43. Hot-spot KIF5A mutations cause familial ALS

44. Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year Study

45. Relationship of serum beta-synuclein with blood biomarkers and brain atrophy

47. Treatment outcome of atypical EGFR mutations in the German National Network Genomic Medicine Lung Cancer (nNGM)

48. Eine Mutation in Atp11a verursacht die autosomal dominant vererbte auditorische Neuropathie Typ 2 (AUNA2).

49. A mutation in Atp11a causes autosomal dominant inherited auditory neuropathy type 2 (AUNA2).

50. Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry

Catalog

Books, media, physical & digital resources