Session

18.03.2022     11:40–12:30

Titel:
Poster Session
Compl / Techno / Therap
Art:
Poster
Raum:
Room 13

18.03.2022
11:40–12:30

Titel:
Poster Session
Compl / Techno / Therap
Art:
Poster
Raum:
Room 13
11:40–11:42
P-Compl-112 Male-pattern hair loss: Integration of GWAS and single-cell RNASeq data to identify pathobiologically relevant hair follicle cell types
Nicole Engelmann (Bonn/DE)
Redezeit: 2 min

11:42–11:44
P-Compl-114 Human-specific ARHGAP11B is essential for neural progenitor levels in hominid brain organoids
Jan Fischer (Dresden/DE)
Redezeit: 2 min

11:44–11:46
P-Compl-116 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
Sabrina Henne (Bonn/DE)
Redezeit: 2 min

11:46–11:48
P-Compl-118 Molecular genetic characterization of patients with bipolar disorder and controls for induced pluripotent stem cell generation
Karola Hünten (Bonn/DE)
Redezeit: 2 min

11:48–11:50
P-Compl-120 SLC1A2 is a new candidate gene for neuromyelitis optica spectrum disorder
Michelle Meyenborg (Kiel/DE)
Redezeit: 2 min

11:50–11:52
P-Compl-122 Association of rare genetic variants at the ULBP3 locus with alopecia areata
Buket Basmanav (), Paula Schwerbrock (Bonn/DE)
Redezeit: 2 min

11:52–11:54
P-Compl-124 Investigation of polygenic risk scores in social anxiety disorder patients
Angelina Vogelsang (Bonn/DE)
Redezeit: 2 min

11:54–11:56
P-Compl-126 Hereditary gelsolin amyloidosis- an Italian family with main finnish mutation
Dorothea Wand (Basel/CH)
Redezeit: 2 min

11:56–11:58
P-Techno-186 A pipeline for NGS-based variant counting applied to assess biomarkers in cfDNA for early detection of second cancers in heritable retinoblastoma
Nicole Barwinski (Essen/DE)
Redezeit: 2 min

11:58–12:00
P-Techno-190 Modernizing GestaltMatcher
Alexander Hustinx (Bonn/DE)
Redezeit: 2 min

12:00–12:02
P-Techno-192 Optimization of assay for transposase-accessible chromatin using sequencing of neutrophils
Janine Klima (Erlangen/DE)
Redezeit: 2 min

12:02–12:04
P-Techno-194 Paralogue annotation of WNT5A enabled identifying a novel pathogenic variant in a family with an autosomal dominant Robinow Syndrome
Shoko Komatsuzaki (Jena/DE)
Redezeit: 2 min

12:04–12:06
P-Techno-196 PTEE resource facilitates the choice of tissue for RNA-seq-based clinical genetics studies
Diana Le Duc (Leipzig/DE)
Redezeit: 2 min

12:06–12:08
P-Techno-198 Implementing RNA analysis in human genetics: from gene expression profiling to integration into genome analysis improvement
Casadei Nicolas (Tübingen/DE)
Redezeit: 2 min

12:08–12:10
P-Techno-200 A new tool in the box: Long-read sequencing in routine diagnostics
Denny Popp (Leipzig/DE)
Redezeit: 2 min

12:10–12:12
P-Techno-202 Highly sensitive Liquid Biopsy Duplex Seq enables molecular diagnosis of a 10 year old child with clinically confirmed overgrowth syndrome in plasma
Julia Romic-Pickl (München/DE)
Redezeit: 2 min

12:12–12:14
P-Techno-204 Classification of fluorescent R-Band metaphase chromosomes using a convolutional neural network is precise and fast in generating karyograms
Beate Vajen (Hannover/DE)
Redezeit: 2 min

12:14–12:16
P-Therap-206 How can whole CFTR genotyping contribute in genetically unsolved Cystic Fibrosis cases?
Julia Hentschel (Leipzig/DE), Simone Ahting (Leipzig/DE)
Redezeit: 2 min