Entries of Sivalingam, Sugirthan on the publication server
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Number of items: 3.
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 and Hilger, Alina C.
(2023)
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations.
European Journal of Human Genetics 31 (1), pp. 105-111.
Fulltext not available.
, 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 and Hilger, Alina C.
(2023)
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations.
European Journal of Human Genetics 31 (1), pp. 105-111.
Fulltext not available.
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. and Mangold, Elisabeth
(2023)
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.
Molecular Genetics & Genomic Medicine 11 (3).
Fulltext not available.
, 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. and Mangold, Elisabeth
(2023)
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.
Molecular Genetics & Genomic Medicine 11 (3).
Fulltext not available.
Jobin, Katarzyna , Stumpf, Natascha E. , Schwab, Sebastian, Eichler, Melanie, Neubert, Patrick, Rauh, Manfred, Adamowski, Marek, Babyak, Olena, Hinze, Daniel, Sivalingam, Sugirthan , Weisheit, Christina, Hochheiser, Katharina, Schmidt, Susanne V., Meissner, Mirjam, Garbi, Natalio, Abdullah, Zeinab, Wenzel, Ulrich, Hölzel, Michael, Jantsch, Jonathan and Kurts, Christian
(2020)
A high-salt diet compromises antibacterial neutrophil responses through hormonal perturbation.
Science Translational Medicine 12 (536), eaay3850.
Fulltext not available.
, Stumpf, Natascha E. , Schwab, Sebastian, Eichler, Melanie, Neubert, Patrick, Rauh, Manfred, Adamowski, Marek, Babyak, Olena, Hinze, Daniel, Sivalingam, Sugirthan , Weisheit, Christina, Hochheiser, Katharina, Schmidt, Susanne V., Meissner, Mirjam, Garbi, Natalio, Abdullah, Zeinab, Wenzel, Ulrich, Hölzel, Michael, Jantsch, Jonathan and Kurts, Christian
(2020)
A high-salt diet compromises antibacterial neutrophil responses through hormonal perturbation.
Science Translational Medicine 12 (536), eaay3850.
Fulltext not available.