Recurrence of Congenital Heart Defects in Families
ØYEN, Nina, POULSEN, Gry, BOYD, Heather A, WOHLFAHRT, Jan, JENSEN, Peter K. A, MELBYE, Mads
Published in Circulation (New York, N.Y.) (28.07.2009)
Published in Circulation (New York, N.Y.) (28.07.2009)
Get full text
Journal Article
Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes
Halgren, Christina, Nielsen, Nete M., Nazaryan-Petersen, Lusine, Silahtaroglu, Asli, Collins, Ryan L., Lowther, Chelsea, Kjaergaard, Susanne, Frisch, Morten, Kirchhoff, Maria, Brøndum-Nielsen, Karen, Lind-Thomsen, Allan, Mang, Yuan, El-Schich, Zahra, Boring, Claire A., Mehrjouy, Mana M., Jensen, Peter K.A., Fagerberg, Christina, Krogh, Lotte N., Hansen, Jan, Bryndorf, Thue, Hansen, Claus, Talkowski, Michael E., Bak, Mads, Tommerup, Niels, Bache, Iben
Published in American journal of human genetics (07.06.2018)
Published in American journal of human genetics (07.06.2018)
Get full text
Journal Article
Recurrence of Discordant Congenital Heart Defects in Families
Øyen, Nina, Poulsen, Gry, Wohlfahrt, Jan, Boyd, Heather A, Jensen, Peter K.A, Melbye, Mads
Published in Circulation. Cardiovascular genetics (01.04.2010)
Published in Circulation. Cardiovascular genetics (01.04.2010)
Get full text
Journal Article
Erwinia amylovora pyrC mutant causes fire blight despite pyrimidine auxotrophy
Ramos, L.S, Sinn, J.P, Lehman, B.L, Pfeufer, E.E, Peter, K.A, McNellis, T.W
Published in Letters in applied microbiology (01.06.2015)
Published in Letters in applied microbiology (01.06.2015)
Get full text
Journal Article
Re-Examination of Danish Carriers of Balanced Chromosomal Inversions
Rasmussen, Malene B, Bache, Iben, Mehrjouy, Mana M, Silahtaroglu, Asli, Kjærgaard, Susanne, Brøndum-Nielsen, Karen, Jensen, Peter K.A, Vogel, Ida, Hertz, Jens Michael, Fagerberg, Christina, Bojesen, Anders, Petersen, Michael B, Hansen, Jan, Halgren, Christina, Bak, Mads, Tommerup, Niels
Published in Cancer genetics (01.05.2016)
Published in Cancer genetics (01.05.2016)
Get full text
Journal Article
Identification of human candidate genes for male infertility by digital differential display
Olesen, Christian, Hansen, Claus, Bendsen, Eske, Byskov, Anne Grete, Schwinger, Eberhard, Lopez-Pajares, Isidora, Jensen, Peter K.A., Kristoffersson, Ulf, Schubert, Regine, Assche, Elvira Van, Wahlstroem, Jan, Lespinasse, James, Tommerup, Niels
Published in Molecular human reproduction (01.01.2001)
Published in Molecular human reproduction (01.01.2001)
Get full text
Journal Article
6 - Re-Examination of Danish Carriers of Balanced Chromosomal Inversions
Rasmussen, Malene B., Bache, Iben, Mehrjouy, Mana M., Silahtaroglu, Asli, Kjærgaard, Susanne, Brøndum-Nielsen, Karen, Jensen, Peter K.A., Vogel, Ida, Hertz, Jens Michael, Fagerberg, Christina, Bojesen, Anders, Petersen, Michael B., Hansen, Jan, Halgren, Christina, Bak, Mads, Tommerup, Niels
Published in Cancer genetics (01.05.2016)
Published in Cancer genetics (01.05.2016)
Get full text
Journal Article
Morphological differentiation and changes in polypeptide synthesis pattern during regeneration of human epidermal tissue developed in vitro
Jensen, Peter K.A., Fey, Stephen J., Larsen, Peter Mose, Nørgård, Jan O.R., Bolund, Lars
Published in Differentiation (London) (01.05.1991)
Published in Differentiation (London) (01.05.1991)
Get full text
Journal Article
Systematic re-examination of carriers of balanced reciprocal translocations: a strategy to search for candidate regions for common and complex diseases
BACHE, Iben, HJORTH, Mads, NIEBUHR, Erik, RASMUSSEN, Kirsten, TOMMERUP, Niels, BUGGE, Merete, HOLSTEBROE, Søren, HILDEN, Jørgen, SCHMIDT, Lone, BRONDUM-NIELSEN, Karen, BRUUN-PETERSEN, Gert, JENSEN, Peter K. A, LUNDSTEEN, Claes
Published in European journal of human genetics : EJHG (01.04.2006)
Published in European journal of human genetics : EJHG (01.04.2006)
Get full text
Journal Article
No signature of Y chromosomal resemblance between possible descendants of the Cimbri in Denmark and Northern Italy
Børglum, Anders D., Vernesi, Cristiano, Jensen, Peter K.A., Madsen, Bo, Haagerup, Annette, Barbujani, Guido
Published in American journal of physical anthropology (01.02.2007)
Published in American journal of physical anthropology (01.02.2007)
Get full text
Journal Article
High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes
Kirchhoff, M, Rose, H, Maahr, J, Gerdes, T, Bugge, M, Tommerup, N, Tümer, Z, Lespinasse, J, Jensen, P K, Wirth, J, Lundsteen, C
Published in European journal of human genetics : EJHG (01.09.2000)
Published in European journal of human genetics : EJHG (01.09.2000)
Get full text
Journal Article
Identification of Novel and Known Mutations in the Genes for Keratin 5 and 14 in Danish Patients with Epidermolysis Bullosa Simplex: Correlation Between Genotype and Phenotype
Sørensen, Charlotte B., Ladekjær-Mikkelsen, Anne-Sofie, Andresen, Brage S., Brandrup, Flemming, Veien, Niels K., Buus, Sanne K., Anton-Lamprecht, Ingrun, Kruse, Torben A., Jensen, Peter K.A., Eiberg, Hans, Bolund, Lars, Gregersen, Niels
Published in Journal of investigative dermatology (01.02.1999)
Published in Journal of investigative dermatology (01.02.1999)
Get full text
Journal Article
Evidence That Mutations in the X-linked DDP Gene Cause Incompletely Penetrant and Variable Skewed X Inactivation
Plenge, Robert M., Tranebjaerg, Lisbeth, Jensen, Peter K.A., Schwartz, Charles, Willard, Huntington F.
Published in American journal of human genetics (01.03.1999)
Published in American journal of human genetics (01.03.1999)
Get full text
Journal Article
Functional testing of keratin 14 mutant proteins associated with the three major subtypes of epidermolysis bullosa simplex
Sørensen, Charlotte B., Andresen, Brage S., Jensen, Uffe B., Jensen, Thomas G., Jensen, Peter K. A., Gregersen, Niels, Bolund, Lars
Published in Experimental dermatology (01.08.2003)
Published in Experimental dermatology (01.08.2003)
Get full text
Journal Article
Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene
Tranebjærg, Lisbeth, Jensen, Peter K.A., Van Ghelue, Marijke, Vnencak-Jones, Cindy L., Sund, Staale, Elgjo, Kjell, Jakobsen, Johannes, Lindal, Sigurd, Warburg, Mette, Fuglsang-Frederiksen, Anders, Skullerud, Kari
Published in Ophthalmic genetics (2001)
Published in Ophthalmic genetics (2001)
Get full text
Journal Article