Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles

por Herrera-Rivero, Marisol, Hochfeld, Lara M., Sivalingam, Sugirthan, Nöthen, Markus M., Heilmann-Heimbach, Stefanie
Publicado 2020

The complete mitochondrial genome of the ‘solar-powered’ sea slug Plakobranchus cf. ocellatus (Heterobranchia: Panpulmonata: Sacoglossa)

por Greve, Carola, Ruiz-Tagle Lui, Maximiliano, Sivalingam, Sugirthan, Ludwig, Kerstin U., Wägele, Heike, Donath, Alexander
Publicado 2017

Gene-based burden scores identify rare variant associations for 28 blood biomarkers

por Aldisi, Rana, Hassanin, Emadeldin, Sivalingam, Sugirthan, Buness, Andreas, Klinkhammer, Hannah, Mayr, Andreas, Fröhlich, Holger, Krawitz, Peter, Maj, Carlo
Publicado 2023

GenRisk: a tool for comprehensive genetic risk modeling

por Aldisi, Rana, Hassanin, Emadeldin, Sivalingam, Sugirthan, Buness, Andreas, Klinkhammer, Hannah, Mayr, Andreas, Fröhlich, Holger, Krawitz, Peter, Maj, Carlo
Publicado 2022

Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss

por Henne, Sabrina Katrin, Aldisi, Rana, Sivalingam, Sugirthan, Hochfeld, Lara Maleen, Borisov, Oleg, Krawitz, Peter Michael, Maj, Carlo, Nöthen, Markus Maria, Heilmann-Heimbach, Stefanie
Publicado 2023

Reconstruction of the origin of the first major SARS-CoV-2 outbreak in Germany

por Korencak, Marek, Sivalingam, Sugirthan, Sahu, Anshupa, Dressen, Dietmar, Schmidt, Axel, Brand, Fabian, Krawitz, Peter, Hart, Libor, Maria Eis-Hübinger, Anna, Buness, Andreas, Streeck, Hendrik
Publicado 2022

Heterogeneity and excitability of BRAF(V600E)-induced tumors is determined by Akt/mTOR-signaling state and Trp53-loss

por Cases-Cunillera, Silvia, van Loo, Karen M J, Pitsch, Julika, Quatraccioni, Anne, Sivalingam, Sugirthan, Salomoni, Paolo, Borger, Valeri, Dietrich, Dirk, Schoch, Susanne, Becker, Albert J
Publicado 2021

Sustained Immunoparalysis in Endotoxin-Tolerized Monocytic Cells

por Weisheit, Christina K., Klüners, Alexandra, Wild, Lennart, Casalter, Alexandra, Heilmann-Heimbach, Stefanie, Sivalingam, Sugirthan, Kleiner, Jan L., Ehrentraut, Stefan F., Hoeft, Andreas, Frede, Stilla, Ehrentraut, Heidi
Publicado 2020

Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia

por Huettmann, Carolina, Stelljes, Matthias, Sivalingam, Sugirthan, Fobker, Manfred, Vrachimis, Alexis, Exler, Anne, Wenning, Christian, Wempe, Carola, Penke, Matthias, Buness, Andreas, Ludwig, Kerstin U., Muckenthaler, Martina U., Steinbicker, Andrea U.
Publicado 2021

TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19

por Schmidt, Axel, Peters, Sophia, Knaus, Alexej, Sabir, Hemmen, Hamsen, Frauke, Maj, Carlo, Fazaal, Julia, Sivalingam, Sugirthan, Savchenko, Oleksandr, Mantri, Aakash, Holzinger, Dirk, Neudorf, Ulrich, Müller, Andreas, Ludwig, Kerstin U., Krawitz, Peter M., Engels, Hartmut, Nöthen, Markus M., Bagci, Soyhan
Publicado 2021

Variant profiling of colorectal adenomas from three patients of two families with MSH3-related adenomatous polyposis

por Perne, Claudia, Peters, Sophia, Cartolano, Maria, Horpaopan, Sukanya, Grimm, Christina, Altmüller, Janine, Sommer, Anna K., Hillmer, Axel M., Thiele, Holger, Odenthal, Margarete, Möslein, Gabriela, Adam, Ronja, Sivalingam, Sugirthan, Kirfel, Jutta, Schweiger, Michal R., Peifer, Martin, Spier, Isabel, Aretz, Stefan
Publicado 2021

Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation

por Witt, Stephanie H., Frank, Josef, Gilles, Maria, Lang, Maren, Treutlein, Jens, Streit, Fabian, Wolf, Isabell A. C., Peus, Verena, Scharnholz, Barbara, Send, Tabea S., Heilmann-Heimbach, Stefanie, Sivalingam, Sugirthan, Dukal, Helene, Strohmaier, Jana, Sütterlin, Marc, Arloth, Janine, Laucht, Manfred, Nöthen, Markus M., Deuschle, Michael, Rietschel, Marcella
Publicado 2018

Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO)

por Schierbaum, Luca M., Schneider, Sophia, Herms, Stefan, Sivalingam, Sugirthan, Fabian, Julia, Reutter, Heiko, Weber, Stefanie, Merz, Waltraut M., Tkaczyk, Marcin, Miklaszewska, Monika, Sikora, Przemyslaw, Szmigielska, Agnieszka, Krzemien, Grazyna, Zachwieja, Katarzyna, Szczepanska, Maria, Taranta-Janusz, Katarzyna, Kroll, Pawel, Polok, Marcin, Zaniew, Marcin, Hilger, Alina C.
Publicado 2021

Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus

por Schulz, Herbert, Ruppert, Ann-Kathrin, Herms, Stefan, Wolf, Christiane, Mirza-Schreiber, Nazanin, Stegle, Oliver, Czamara, Darina, Forstner, Andreas J., Sivalingam, Sugirthan, Schoch, Susanne, Moebus, Susanne, Pütz, Benno, Hillmer, Axel, Fricker, Nadine, Vatter, Hartmut, Müller-Myhsok, Bertram, Nöthen, Markus M., Becker, Albert J., Hoffmann, Per, Sander, Thomas, Cichon, Sven
Publicado 2017

Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study

por Krug, Axel, Wöhr, Markus, Seffer, Dominik, Rippberger, Henrike, Sungur, A. Özge, Dietsche, Bruno, Stein, Frederike, Sivalingam, Sugirthan, Forstner, Andreas J., Witt, Stephanie H., Dukal, Helene, Streit, Fabian, Maaser, Anna, Heilmann-Heimbach, Stefanie, Andlauer, Till F. M., Herms, Stefan, Hoffmann, Per, Rietschel, Marcella, Nöthen, Markus M., Lackinger, Martin, Schratt, Gerhard, Koch, Michael, Schwarting, Rainer K. W., Kircher, Tilo
Publicado 2020

Exome sequencing in large, multiplex bipolar disorder families from Cuba

por Maaser, Anna, Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Ludwig, Kerstin U., Sivalingam, Sugirthan, Streit, Fabian, Degenhardt, Franziska, Witt, Stephanie H., Reinbold, Céline S., Koller, Anna C., Raff, Ruth, Heilmann-Heimbach, Stefanie, Fischer, Sascha B., Herms, Stefan, Hoffmann, Per, Thiele, Holger, Nürnberg, Peter, Löhlein Fier, Heide, Orozco-Díaz, Guillermo, Carmenate-Naranjo, Deinys, Proenza-Barzaga, Niurka, Auburger, Georg W. J., Andlauer, Till F. M., Cichon, Sven, Marcheco-Teruel, Beatriz, Mors, Ole, Rietschel, Marcella, Nöthen, Markus M.
Publicado 2018

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations

por Fabian, Julia, Dworschak, Gabriel C., Waffenschmidt, Lea, Schierbaum, Luca, Bendixen, Charlotte, Heilmann-Heimbach, Stefanie, Sivalingam, Sugirthan, Buness, Andreas, Schwarzer, Nicole, Boemers, Thomas M., Schmiedeke, Eberhard, Neser, Jörg, Leonhardt, Johannes, Kosch, Ferdinand, Weih, Sandra, Gielen, Helen Maya, Hosie, Stuart, Kabs, Carmen, Palta, Markus, Märzheuser, Stefanie, Bode, Lena Marie, Lacher, Martin, Schäfer, Frank-Mattias, Stehr, Maximilian, Knorr, Christian, Ure, Benno, Kleine, Katharina, Rolle, Udo, Zaniew, Marcin, Phillip, Grote, Zwink, Nadine, Jenetzky, Ekkehart, Reutter, Heiko, Hilger, Alina C.
Publicado 2022

Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores

por Ishorst, Nina, Henschel, Leonie, Thieme, Frederic, Drichel, Dmitriy, Sivalingam, Sugirthan, Mehrem, Sarah L., Fechtner, Ariane C., Fazaal, Julia, Welzenbach, Julia, Heimbach, André, Maj, Carlo, Borisov, Oleg, Hausen, Jonas, Raff, Ruth, Hoischen, Alexander, Dixon, Michael, Rada‐Iglesias, Alvaro, Bartusel, Michaela, Rojas‐Martinez, Augusto, Aldhorae, Khalid, Braumann, Bert, Kruse, Teresa, Kirschneck, Christian, Spanier, Gerrit, Reutter, Heiko, Nowak, Stefanie, Gölz, Lina, Knapp, Michael, Buness, Andreas, Krawitz, Peter, Nöthen, Markus M., Nothnagel, Michael, Becker, Tim, Ludwig, Kerstin U., Mangold, Elisabeth
Publicado 2022

The role of environmental stress and DNA methylation in the longitudinal course of bipolar disorder

por Comes, Ashley L., Czamara, Darina, Adorjan, Kristina, Anderson-Schmidt, Heike, Andlauer, Till F. M., Budde, Monika, Gade, Katrin, Hake, Maria, Kalman, Janos L., Papiol, Sergi, Reich-Erkelenz, Daniela, Klöhn-Saghatolislam, Farah, Schaupp, Sabrina K., Schulte, Eva C., Senner, Fanny, Juckel, Georg, Schmauß, Max, Zimmermann, Jörg, Reimer, Jens, Reininghaus, Eva, Anghelescu, Ion-George, Konrad, Carsten, Thiel, Andreas, Figge, Christian, von Hagen, Martin, Koller, Manfred, Dietrich, Detlef E., Stierl, Sebastian, Scherk, Harald, Witt, Stephanie H., Sivalingam, Sugirthan, Degenhardt, Franziska, Forstner, Andreas J., Rietschel, Marcella, Nöthen, Markus M., Wiltfang, Jens, Falkai, Peter, Schulze, Thomas G., Heilbronner, Urs
Publicado 2020

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

por Forstner, Andreas J., Fischer, Sascha B., Schenk, Lorena M., Strohmaier, Jana, Maaser-Hecker, Anna, Reinbold, Céline S., Sivalingam, Sugirthan, Hecker, Julian, Streit, Fabian, Degenhardt, Franziska, Witt, Stephanie H., Schumacher, Johannes, Thiele, Holger, Nürnberg, Peter, Guzman-Parra, José, Orozco Diaz, Guillermo, Auburger, Georg, Albus, Margot, Borrmann-Hassenbach, Margitta, González, Maria José, Gil Flores, Susana, Cabaleiro Fabeiro, Francisco J., del Río Noriega, Francisco, Perez Perez, Fermin, Haro González, Jesus, Rivas, Fabio, Mayoral, Fermin, Bauer, Michael, Pfennig, Andrea, Reif, Andreas, Herms, Stefan, Hoffmann, Per, Pirooznia, Mehdi, Goes, Fernando S., Rietschel, Marcella, Nöthen, Markus M., Cichon, Sven
Publicado 2020