Are there anxious genes?

por Morris-Rosendahl, Deborah J.
Publicado 2002

A glossary of relevant genetic terms

por Morris-Rosendahl, Deborah J.
Publicado 2010

The future of genetic testing for drug response

por Morris-Rosendahl, Deborah J., Fiebich, Bernd L.
Publicado 2004

The role of genetics and genomics in clinical psychiatry

por Hoehe, Margret R., Morris-Rosendahl, Deborah J.
Publicado 2018

Neurodevelopmental disorders—the history and future of a diagnostic concept


por Morris-Rosendahl, Deborah J., Crocq, Marc-Antoine
Publicado 2020

Cystic Fibrosis Lung Disease Modifiers and Their Relevance in the New Era of Precision Medicine

por Sepahzad, Afsoon, Morris-Rosendahl, Deborah J., Davies, Jane C.
Publicado 2021

Long QT and Silver Russell syndrome: First case report in a 9-year-old girl

por Roses-Noguer, Ferran, Martinez-Villar, Maria, Honti, Frank, Edwards, Matthew, Till, Jan, Morris-Rosendahl, Deborah J.
Publicado 2020

Lethal course of meconium ileus in preterm twins revealing a novel cystic fibrosis mutation (p.Cys524Tyr)

por Puzik, Alexander, Morris-Rosendahl, Deborah J, Rückauer, Klaus-Dieter, Otto, Claudia, Gessler, Peter, Saueressig, Ulrich, Hentschel, Roland
Publicado 2014

A mutation creating an upstream initiation codon in the SOX9 5′ UTR causes acampomelic campomelic dysplasia

por von Bohlen, Anna E., Böhm, Johann, Pop, Ramona, Johnson, Diana S., Tolmie, John, Stücker, Ralf, Morris‐Rosendahl, Deborah, Scherer, Gerd
Publicado 2017

Evaluation of a novel rapid genomic test including polygenic risk scores for the diagnosis and management of familial hypercholesterolaemia

por Neves, Emma, Khan, Tina, Williams, Maggie, Carrera, Marta, Banya, Winston, Brugada, Ramon, Ferrer, Carles, Morris-Rosendahl, Deborah J, Barbir, Mahmoud
Publicado 2021

Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation

por Issa, Lina, Mueller, Katrin, Seufert, Katja, Kraemer, Nadine, Rosenkotter, Henning, Ninnemann, Olaf, Buob, Michael, Kaindl, Angela M, Morris-Rosendahl, Deborah J
Publicado 2013

Metabolomic, transcriptomic and genetic integrative analysis reveals important roles of adenosine diphosphate in haemostasis and platelet activation in non‐small‐cell lung cancer...

por Hoang, Long T., Domingo‐Sabugo, Clara, Starren, Elizabeth S., Willis‐Owen, Saffron A.G., Morris‐Rosendahl, Deborah J., Nicholson, Andrew G., Cookson, William O. C. M., Moffatt, Miriam F.
Publicado 2019

EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias

por Hayesmoore, Jesse B., Bhuiyan, Zahurul A., Coviello, Domenico A., du Sart, Desirée, Edwards, Matthew, Iascone, Maria, Morris-Rosendahl, Deborah J., Sheils, Katie, van Slegtenhorst, Marjon, Thomson, Kate L.
Publicado 2023

The addition of genetic testing and cardiovascular magnetic resonance to routine clinical data for stratification of etiology in dilated cardiomyopathy

por Amin, Ravi J., Morris-Rosendahl, Deborah, Edwards, Mat, Tayal, Upasana, Buchan, Rachel, Hammersley, Daniel J., Jones, Richard E., Gati, Sabiha, Khalique, Zohya, Almogheer, Batool, Pennell, Dudley J., Baksi, Arun John, Pantazis, Antonis, Ware, James S., Prasad, Sanjay K., Halliday, Brian P.
Publicado 2022

BRF1 mutations alter RNA polymerase III–dependent transcription and cause neurodevelopmental anomalies

por Borck, Guntram, Hög, Friederike, Dentici, Maria Lisa, Tan, Perciliz L., Sowada, Nadine, Medeira, Ana, Gueneau, Lucie, Thiele, Holger, Kousi, Maria, Lepri, Francesca, Wenzeck, Larissa, Blumenthal, Ian, Radicioni, Antonio, Schwarzenberg, Tito Livio, Mandriani, Barbara, Fischetto, Rita, Morris-Rosendahl, Deborah J., Altmüller, Janine, Reymond, Alexandre, Nürnberg, Peter, Merla, Giuseppe, Dallapiccola, Bruno, Katsanis, Nicholas, Cramer, Patrick, Kubisch, Christian
Publicado 2015

Integrated genomics point to immune vulnerabilities in pleural mesothelioma

por Nastase, Anca, Mandal, Amit, Lu, Shir Kiong, Anbunathan, Hima, Morris-Rosendahl, Deborah, Zhang, Yu Zhi, Sun, Xiao-Ming, Gennatas, Spyridon, Rintoul, Robert C., Edwards, Matthew, Bowman, Alex, Chernova, Tatyana, Benepal, Tim, Lim, Eric, Taylor, Anthony Newman, Nicholson, Andrew G., Popat, Sanjay, Willis, Anne E., MacFarlane, Marion, Lathrop, Mark, Bowcock, Anne M., Moffatt, Miriam F., Cookson, William O. C. M.
Publicado 2021

Author Correction: Integrated genomics point to immune vulnerabilities in pleural mesothelioma

por Nastase, Anca, Mandal, Amit, Lu, Shir Kiong, Anbunathan, Hima, Morris‑Rosendahl, Deborah, Zhang, Yu Zhi, Sun, Xiao‑Ming, Gennatas, Spyridon, Rintoul, Robert C., Edwards, Matthew, Bowman, Alex, Chernova, Tatyana, Benepal, Tim, Lim, Eric, Taylor, Anthony Newman, Nicholson, Andrew G., Popat, Sanjay, Willis, Anne E., MacFarlane, Marion, Lathrop, Mark, Bowcock, Anne M., Moffatt, Miriam F., Cookson, William O. C. M.
Publicado 2022

Mutations in STAMBP, encoding a deubiquitinating enzyme, cause Microcephaly-Capillary Malformation syndrome

por McDonell, Laura M., Mirzaa, Ghayda M., Alcantara, Diana, Schwartzentruber, Jeremy, Carter, Melissa T., Lee, Leo J., Clericuzio, Carol L., Graham, John M., Morris-Rosendahl, Deborah J., Polster, Tilman, Acsadi, Gyula, Townshend, Sharron, Williams, Simon, Halbert, Anne, Isidor, Bertrand, Smyser, Christopher D., Paciorkowski, Alex R., Willing, Marcia, Woulfe, John, Das, Soma, Beaulieu, Chandree L., Marcadier, Janet, Geraghty, Michael T., Frey, Brendan J., Majewski, Jacek, Bulman, Dennis E., Dobyns, William B., O’Driscoll, Mark, Boycott, Kym M.
Publicado 2013

PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families

por Guimier, Anne, Achleitner, Melanie T., Moreau de Bellaing, Anne, Edwards, Matthew, de Pontual, Loïc, Mittal, Kirti, Dunn, Kyla E., Grove, Megan E., Tysoe, Carolyn J., Dimartino, Clémantine, Cameron, Jessie, Kanthi, Anil, Shukla, Anju, van den Broek, Florence, Chatterjee, Diptendu, Alston, Charlotte L., Knowles, Charlotte V., Brett, Laura, Till, Jan A., Homfray, Tessa, French, Paul, Spentzou, Georgia, Elserafy, Noha A., Lichkus, Kate S., Sankaran, Bindu P., Kennedy, Hannah L., George, Peter M., Kidd, Alexa, Wortmann, Saskia B., Fisk, Dianna G., Koopmann, Tamara T., Rafiq, Muhammad A., Merker, Jason D., Parikh, Sumith, Ahimaz, Priyanka, Weintraub, Robert G., Ma, Alan S., Turner, Christian, Ellaway, Carolyn J., Phillips, Liza K., Thorburn, David R., Chung, Wendy K., Kana, Sajel L., Faye-Petersen, Ona M., Thompson, Michelle L., Janin, Alexandre, McLeod, Karen, McGowan, Ruth, McFarland, Robert, Girisha, Katta M., Morris-Rosendahl, Deborah J., Hurst, Anna C. E., Turner, Claire L. S., Hamilton, Robert M., Taylor, Robert W., Bajolle, Fanny, Gordon, Christopher T., Amiel, Jeanne, Mayr, Johannes A., Doudney, Kit
Publicado 2021