Connection
Co-Authors
This is a "connection" page, showing publications co-authored by Florian Kraft and Ingo Kurth.
Connection Strength
1,956
-
Long-read sequencing to understand genome biology and cell function. Int J Biochem Cell Biol. 2020 09; 126:105799.
Score: 0,761
-
Closing the Gap - Detection of 5q-Spinal Muscular Atrophy by Short-Read Next-Generation Sequencing and Unexpected Results in a Diagnostic Patient Cohort. J Neuromuscul Dis. 2023; 10(5):835-846.
Score: 0,226
-
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3. Nat Commun. 2019 10 29; 10(1):4919.
Score: 0,181
-
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation. Clin Epigenetics. 2019 02 15; 11(1):30.
Score: 0,173
-
DEGS1-associated aberrant sphingolipid metabolism impairs nervous system function in humans. J Clin Invest. 2019 03 01; 129(3):1229-1239.
Score: 0,173
-
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach. Clin Epigenetics. 2023 03 01; 15(1):35.
Score: 0,057
-
Functional connectivity signatures of NMDAR dysfunction in schizophrenia-integrating findings from imaging genetics and pharmaco-fMRI. Transl Psychiatry. 2023 02 16; 13(1):59.
Score: 0,057
-
Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. Eur J Hum Genet. 2021 11; 29(11):1663-1668.
Score: 0,051
-
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation. J Clin Invest. 2021 06 15; 131(12).
Score: 0,051
-
Inherited cases of CNOT3-associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies. Clin Genet. 2020 10; 98(4):408-412.
Score: 0,048
-
Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles. Brain. 2020 08 01; 143(8):2406-2420.
Score: 0,048
-
Germline GPR161 Mutations Predispose to Pediatric Medulloblastoma. J Clin Oncol. 2020 01 01; 38(1):43-50.
Score: 0,045
-
Familial NEDD4L variant in periventricular nodular heterotopia and in a fetus with hypokinesia and flexion contractures. Mol Genet Genomic Med. 2018 11; 6(6):1255-1260.
Score: 0,042
-
Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers. Eur J Hum Genet. 2019 01; 27(1):42-48.
Score: 0,042
