Risk of Adverse Pregnancy Outcomes at Advanced Maternal Age
Frederiksen, Line Elmerdahl, Ernst, Andreas, Brix, Nis, Braskhøj Lauridsen, Lea Lykke, Roos, Laura, Ramlau-Hansen, Cecilia Høst, Ekelund, Charlotte Kvist
Published in Obstetrics and gynecology (New York. 1953) (01.03.2018)
Published in Obstetrics and gynecology (New York. 1953) (01.03.2018)
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Journal Article
Causes of poor eye contact in infants: a population-based study
Levinsen, Mette, Børresen, Malene Landbo, Roos, Laura, Grønskov, Karen, Kessel, Line
Published in BMC ophthalmology (07.11.2021)
Published in BMC ophthalmology (07.11.2021)
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Journal Article
Is MED13L-related intellectual disability a recognizable syndrome?
Tørring, Pernille Mathiesen, Larsen, Martin Jakob, Brasch-Andersen, Charlotte, Krogh, Lotte Nylandsted, Kibæk, Maria, Laulund, Lone, Illum, Niels, Dunkhase-Heinl, Ulrike, Wiesener, Antje, Popp, Bernt, Marangi, Giuseppe, Hjortshøj, Tina Duelund, Ek, Jakob, Vogel, Ida, Becher, Naja, Roos, Laura, Zollino, Marcella, Fagerberg, Christina Ringmann
Published in European journal of medical genetics (01.02.2019)
Published in European journal of medical genetics (01.02.2019)
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Journal Article
Refinement of genotype-phenotype correlation in 18 patients carrying a 1q24q25 deletion
Chatron, Nicolas, Haddad, Véronique, Andrieux, Joris, Désir, Julie, Boute, Odile, Dieux, Anne, Baumann, Clarisse, Drunat, Séverine, Gérard, Marion, Bonnet, Céline, Leheup, Bruno, Till, Marianne, Rossi, Massimiliano, Flori, Elisabeth, Alembik, Yves, Stewart, Helen, McParland, Joanna, Bernardini, Laura, Castelluccio, Pia, Roos, Laura, Tümer, Zeynep, Fagan, Kerry, Hackett, Anna, Bain, Nicole, van Haeringen, Arie, Ruivenkamp, Claudia, Benzacken, Brigitte, Sanlaville, Damien, Edery, Patrick, Aboura, Azzedine, Schluth-Bolard, Caroline
Published in American journal of medical genetics. Part A (01.05.2015)
Published in American journal of medical genetics. Part A (01.05.2015)
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Journal Article
Epidemiology of ectopia lentis and outcomes after surgery in a Danish population
Rasul, Asrin, Roos, Laura, Groth, Kristian, Riise, Per, Bach-Holm, Daniella, Kessel, Line
Published in Journal of cataract and refractive surgery (01.12.2022)
Published in Journal of cataract and refractive surgery (01.12.2022)
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Journal Article
Maternal age and the risk of fetal aneuploidy: A nationwide cohort study of more than 500000 singleton pregnancies in Denmark from 2008 to 2017
Frederiksen, Line Elmerdahl, Ølgaard, Sofie Møller, Roos, Laura, Petersen, Olav Bjørn, Rode, Line, Hartwig, Tanja, Charlotte Kvist Ekelund, Vogel, Ida
Published in Acta obstetricia et gynecologica Scandinavica (01.02.2024)
Published in Acta obstetricia et gynecologica Scandinavica (01.02.2024)
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Journal Article
Genetic disease is a common cause of bilateral childhood cataract in Denmark
Kessel, Line, Bach-Holm, Daniella, Al-Bakri, Moug, Roos, Laura, Lund, Allan, Grønskov, Karen
Published in Ophthalmic genetics (01.12.2021)
Published in Ophthalmic genetics (01.12.2021)
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Journal Article
Maternal age and the risk of fetal aneuploidy: A nationwide cohort study of more than 500 000 singleton pregnancies in Denmark from 2008 to 2017
Elmerdahl Frederiksen, Line, Ølgaard, Sofie Møller, Roos, Laura, Petersen, Olav Bjørn, Rode, Line, Hartwig, Tanja, Ekelund, Charlotte Kvist, Vogel, Ida
Published in Acta obstetricia et gynecologica Scandinavica (01.02.2024)
Published in Acta obstetricia et gynecologica Scandinavica (01.02.2024)
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Journal Article
Congenital Microphthalmia, Anophthalmia and Coloboma among Live Births in Denmark
Roos, Laura, Jensen, Hanne, Grønskov, Karen, Holst, René, Tümer, Zeynep
Published in Ophthalmic epidemiology (02.09.2016)
Published in Ophthalmic epidemiology (02.09.2016)
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Journal Article
Direct to consumer genetic testing in Denmark-public knowledge, use, and attitudes
Gerdes, Anne-Marie, Nicolaisen, Line, Husum, Egil, Andersen, Janne Bayer, Gantzhorn, Martin Dræbye, Roos, Laura, Diness, Birgitte Rode
Published in European journal of human genetics : EJHG (01.05.2021)
Published in European journal of human genetics : EJHG (01.05.2021)
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Journal Article
Preimplantation genetic testing practices in the Nordic countries
Hreinsson, Julius, Iwarsson, Erik, Hanson, Charles, Grøndahl, Marie Louise, Løssl, Kristine, Hydén‐Granskog, Christel, Ingerslev, Hans Jakob, Petersen, Morten Rønn, Bredbacka, Peter, Nøhr, Bugge, Savolainen, Linda, Hnida, Christina, Toft, Christian Liebst Frisk, Hindkjær, Johnny, Aagaard, Jørn, Lundin, Kersti, Roos, Laura Kirstine Sønderberg
Published in Acta obstetricia et gynecologica Scandinavica (01.06.2020)
Published in Acta obstetricia et gynecologica Scandinavica (01.06.2020)
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Journal Article
Genetic screening of prospective parents
Smed, Vibe Madsen, Petersen, Olav Bennike Bjørn, Gerdes, Anne-Marie Axø, Diness, Birgitte Rode, Roos, Laura Sønderberg
Published in Ugeskrift for læger (29.03.2021)
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Published in Ugeskrift for læger (29.03.2021)
Journal Article
Genetic screening of adopted individuals
Wriedt, Tanja Røhmer, Gerdes, Anne-Marie Axø, Roos, Laura Kristine, Hammer-Hansen, Sophia, Christensen, Maja Bejerholm, Diness, Birgitte Rode
Published in Ugeskrift for læger (29.03.2021)
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Published in Ugeskrift for læger (29.03.2021)
Journal Article
The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes
Curry, Cynthia J., Rosenfeld, Jill A., Grant, Erica, Gripp, Karen W., Anderson, Carol, Aylsworth, Arthur S., Saad, Taha Ben, Chizhikov, Victor V., Dybose, Giedre, Fagerberg, Christina, Falco, Michelle, Fels, Christina, Fichera, Marco, Graakjaer, Jesper, Greco, Donatella, Hair, Jennifer, Hopkins, Elizabeth, Huggins, Marlene, Ladda, Roger, Li, Chumei, Moeschler, John, Nowaczyk, Malgorzata J.M., Ozmore, Jillian R., Reitano, Santina, Romano, Corrado, Roos, Laura, Schnur, Rhonda E., Sell, Susan, Suwannarat, Pim, Svaneby, Dea, Szybowska, Marta, Tarnopolsky, Mark, Tervo, Raymond, Tsai, Anne Chun-Hui, Tucker, Megan, Vallee, Stephanie, Wheeler, Ferrin C, Zand, Dina J., Barkovich, A. James, Aradhya, Swaroop, Shaffer, Lisa G., Dobyns, William B.
Published in American journal of medical genetics. Part A (01.08.2013)
Published in American journal of medical genetics. Part A (01.08.2013)
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Journal Article
Pontocerebellar hypoplasia is a rare cause of floppy infant syndrome
Christiansen, Susanne, Roos, Laura Kirstine Sønderberg, Miranda, Maria J
Published in Ugeskrift for læger (28.09.2015)
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Published in Ugeskrift for læger (28.09.2015)
Journal Article