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Ludwig, Kerstin U
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1

TMPRSS2 isoform 1 downregulation by G-quadruplex stabilizat..:

De Magis, Alessio ; Schult, Philipp ; Schönleber, Antonia...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10773119/.  , 2024
Link: http://www.ncbi.nlm.nih...
 
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2

Pancreatic cancer acquires resistance to MAPK pathway inhib..:

Godfrey, Laura K ; Forster, Jan ; Liffers, Sven-Thorsten...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10792938/.  , 2024
Link: http://www.ncbi.nlm.nih...
 
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3

Identification of de novo variants in nonsyndromic cleft li..:

Ishorst, Nina ; Henschel, Leonie ; Thieme, Frederic...
Publisher's version.  , 2023
Link: http://hdl.handle.net/10..
 
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4

Exome-wide association study to identify rare variants infl..:

Butler-Laporte, Guillaume ; Povysil, Gundula ; Kosmicki, Jack A...
10.1371/journal.pgen.1010367.  , 2023
Link: http://hdl.handle.net/10..
 
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5

Analysis of candidate genes for cleft lip ± cleft palate us..:

Siewert, Anna ; Reiz, Benedikt ; Krug, Carina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165499/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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6

A second update on mapping the human genetic architecture o..:

Kanai, Masahiro ; Andrews, Shea J ; Cordioli, Mattia...
info:eu-repo/semantics/altIdentifier/doi/10.1038/S41586-023-06355-3.  , 2023
Link: https://investigacion.un..
 
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7

A second update on mapping the human genetic architecture o..:

Kanai, Masahiro ; Andrews, Shea J ; Cordioli, Mattia...
info:eu-repo/semantics/altIdentifier/pmid/37674002.  , 2023
Link: https://hdl.handle.net/2..
 
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8

Identification of de novo variants in nonsyndromic cleft li..:

Ishorst, Nina ; Henschel, Leonie ; Thieme, Frederic...
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/22675.  , 2023
Link: https://opus4.kobv.de/op..
 
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9

Genome-wide association study reveals new insights into the..:

Gialluisi, Alessandro ; Andlauer, Till F. M ; Mirza-Schreiber, Nazanin...
10.1038/s41380-020-00898-x.  , 2023
Link: http://hdl.handle.net/10..
 
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10

Common, low-frequency, rare, and ultra-rare coding variants..:

Fallerini, Chiara ; Picchiotti, Nicola ; Baldassarri, Margherita...
https://www.repository.cam.ac.uk/handle/1810/335997.  , 2022
Link: https://www.repository.c..
 
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11

Exome-wide association study to identify rare variants infl..:

Butler-Laporte, Guillaume ; Povysil, Gundula ; Kosmicki, Jack A...
https://mediatum.ub.tum.de/1733277.  , 2022
Link: https://mediatum.ub.tum...
 
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12

Common, low-frequency, rare, and ultra-rare coding variants..:

Fallerini, Chiara ; Picchiotti, Nicola ; Baldassarri, Margherita...
info:eu-repo/semantics/altIdentifier/pmid/34889978.  , 2022
Link: http://hdl.handle.net/11..
 
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13

Exome-wide association study to identify rare variants infl..:

Butler-Laporte, Guillaume ; Povysil, Gundula ; Kosmicki, Jack A...
info:eu-repo/semantics/altIdentifier/pmid/36327219.  , 2022
Link: https://hdl.handle.net/1..
 
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14

Prioritization of non-coding elements involved in non-syndr..:

Zieger, Hanna K ; Weinhold, Leonie ; Schmidt, Axel...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795529/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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15

A genome-wide association study with tissue transcriptomics..:

Mingardo, Enrico ; Beaman, Glenda ; Grote, Philip...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646906/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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