Kerstin Nöthen: search on Z-Library

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1

Nonsyndromic cleft lip with or without cleft palate in arab populations: Genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen

Aldhorae, Khalid Ahmed, Böhmer, Anne C., Ludwig, Kerstin U., Esmail, Ahlam Hibatulla Ali, Al-Hebshi, Nezar Noor, Lippke, Bärbel, Gölz, Lina, Nöthen, Markus M., Daratsianos, Nikolaos, Knapp, Michael, J

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2014

Language:

english

File:

PDF, 99 KB

english, 2014

2

Gas hydrate decomposition recorded by authigenic barite at pockmark sites of the northern Congo Fan

Kasten, Sabine, Nöthen, Kerstin, Hensen, Christian, Spieß, Volkhard, Blumenberg, Martin, Schneider, Ralph R.

Journal:

Geo-Marine Letters

Year:

2012

Language:

english

File:

PDF, 481 KB

english, 2012

3

Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients

Tiit Nikopensius, Stefanie Birnbaum, Kerstin U. Ludwig, Triin Jagomägi, Mare Saag, Stefan Herms, Michael Knapp, Per Hoffmann, Markus M. Nöthen, Andres Metspalu, Elisabeth Mangold

Journal:

European Journal of Oral Sciences

Year:

2010

Language:

english

File:

PDF, 94 KB

english, 2010

4

Diagenetic barium cycling in Black Sea sediments – A case study for anoxic marine environments

Susann Henkel, José M. Mogollón, Kerstin Nöthen, Christine Franke, Kara Bogus, Eric Robin, André Bahr, Martin Blumenberg, Thomas Pape, Richard Seifert, Christian März, Gert J. de Lange, Sabine Kasten

Journal:

Geochimica et Cosmochimica Acta

Year:

2012

Language:

english

File:

PDF, 2.13 MB

english, 2012

5

Investigation of dominant and recessive inheritance models in GWAS data of nonsyndromic cleft lip with or without cleft palate

Böhmer, Anne C., Gölz, Lina, Kreusch, Thomas, Kramer, Franz-Josef, Pötzsch, Bernd, Nöthen, Markus M., Jäger, Andreas, Mangold, Elisabeth, Knapp, Michael, Ludwig, Kerstin U.

Journal:

Birth Defects Research

Year:

2017

Language:

english

File:

PDF, 372 KB

english, 2017

6

Die Rolle seltener Varianten bei häufigen Krankheiten; The role of rare variants in common diseases;

Ludwig, Kerstin U., Degenhardt, Franziska, Nöthen, Markus M.

Journal:

medizinische genetik

Year:

2019

Language:

german

File:

PDF, 1.97 MB

german, 2019

7

Breakthroughs in the genetics of orofacial clefting

Elisabeth Mangold, Kerstin U. Ludwig, Markus M. Nöthen

Journal:

Trends in Molecular Medicine

Year:

2011

Language:

english

File:

PDF, 942 KB

english, 2011

8

Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety

Forstner, Andreas J., Rambau, Stefanie, Friedrich, Nina, Ludwig, Kerstin U., Böhmer, Anne C., Mangold, Elisabeth, Maaser, Anna, Hess, Timo, Kleiman, Alexandra, Bittner, Antje, Nöthen, Markus M., Becke

Journal:

Psychiatric Genetics

Year:

2017

Language:

english

File:

PDF, 166 KB

english, 2017

9

Brain–gene interactions in dyslexia

G. Schulte-Körne, J. Bruder, N. Neuhoff, D. Roeske, P. Hoffmann, Kerstin Ludwig, M.M. Nöthen, B. Müller-Myhsok

Journal:

International Journal of Psychophysiology

Year:

2010

Language:

english

File:

PDF, 62 KB

english, 2010

10

Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population

Ludwig, Kerstin U., Wahle, Philipp, Reutter, Heiko, Paredes-Zenteno, Mario, Muñoz-Jimenez, Sergio G., Ortiz-Lopez, Rocio, Böhmer, Anne C., Tessmann, Peter, Nowak, Stefanie, Nöthen, Markus M., Knapp, M

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2014

Language:

english

File:

PDF, 74 KB

english, 2014

11

Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population

Cura, Francesca, Böhmer, Anne C., Klamt, Johanna, Schünke, Hannah, Scapoli, Luca, Martinelli, Marcella, Carinci, Francesco, Nöthen, Markus M., Knapp, Michael, Ludwig, Kerstin U., Mangold, Elisabeth

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2016

Language:

english

File:

PDF, 90 KB

english, 2016

12

Investigation of interaction betweenDCDC2andKIAA0319in a large German dyslexia sample

Kerstin U. Ludwig, Darina Roeske, Johannes Schumacher, Gerd Schulte-Körne, Inke R. König, Andreas Warnke, Ellen Plume, Andreas Ziegler, Helmut Remschmidt, Bertram Müller-Myhsok, Markus M. Nöthen, Per

Journal:

Journal of Neural Transmission

Year:

2008

Language:

english

File:

PDF, 143 KB

english, 2008

13

Genetics and Neuroscience in Dyslexia: Perspectives for Education and Remediation

Gerd Schulte-Körne, Kerstin U. Ludwig, Jennifer El Sharkawy, Markus M. Nöthen, Bertram Müller-Myhsok, Per Hoffmann

Journal:

Mind Brain and Education

Year:

2007

Language:

english

File:

PDF, 250 KB

english, 2007

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