Maternal obesity and metabolic disorders associate with congenital heart defects in the offspring: A systematic review

por Hedermann, Gitte, Hedley, Paula L., Thagaard, Ida N., Krebs, Lone, Ekelund, Charlotte Kvist, Sørensen, Thorkild I. A., Christiansen, Michael
Publicado no PLoS One (2021)

The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study

por Hedley, Paula L, Haundrup, Ole, Andersen, Paal S, Aidt, Frederik H, Jensen, Morten, Moolman-Smook, Johanna C, Bundgaard, Henning, Christiansen, Michael
Publicado em 2011

MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndrome

por Hedley, Paula L., Carlsen, Anting L., Christiansen, Kasper M., Kanters, Jørgen K., Behr, Elijah R., Corfield, Valerie A., Christiansen, Michael
Publicado em 2014

The Role of Leptin in Fetal Growth during Pre-Eclampsia

por de Knegt, Victoria E., Hedley, Paula L., Kanters, Jørgen K., Thagaard, Ida N., Krebs, Lone, Christiansen, Michael, Lausten-Thomsen, Ulrik
Publicado no Int J Mol Sci (2021)

Fc Gamma Receptor IIIB (FcγRIIIB) Polymorphisms Are Associated with Clinical Malaria in Ghanaian Children

por Adu, Bright, Dodoo, Daniel, Adukpo, Selorme, Hedley, Paula L., Arthur, Fareed K. N., Gerds, Thomas A., Larsen, Severin O., Christiansen, Michael, Theisen, Michael
Publicado em 2012

Private Mitochondrial DNA Variants in Danish Patients with Hypertrophic Cardiomyopathy

por Hagen, Christian M., Aidt, Frederik H., Havndrup, Ole, Hedley, Paula L., Jensen, Morten K., Kanters, Jørgen K., Pham, Tam T., Bundgaard, Henning, Christiansen, Michael
Publicado no PLoS One (2015)

Polymorphisms in the RNASE3 Gene Are Associated with Susceptibility to Cerebral Malaria in Ghanaian Children

por Adu, Bright, Dodoo, Daniel, Adukpo, Selorme, Gyan, Ben A., Hedley, Paula L., Goka, Bamenla, Adjei, George O., Larsen, Severin O., Christiansen, Michael, Theisen, Michael
Publicado em 2011

Long QT syndrome in South Africa: the results of comprehensive genetic screening

por Hedley, Paula L, Durrheim, Glenda A, Hendricks, Firzana, Corfield, Valerie A, Jespersgaard, Cathrine, Støvring, Birgitte, Pham, Tam T, Christiansen, Michael, Goosen, Althea, Brink, Paul A
Publicado em 2013

Mitochondrial Haplogroups Modify the Risk of Developing Hypertrophic Cardiomyopathy in a Danish Population

por Hagen, Christian M., Aidt, Frederik H., Hedley, Paula L., Jensen, Morten K., Havndrup, Ole, Kanters, Jørgen K., Moolman-Smook, Johanna C., Larsen, Severin O., Bundgaard, Henning, Christiansen, Michael
Publicado em 2013

MT-CYB mutations in hypertrophic cardiomyopathy

por Hagen, Christian M, Aidt, Frederik H, Havndrup, Ole, Hedley, Paula L, Jespersgaard, Cathrine, Jensen, Morten, Kanters, Jørgen K, Moolman-Smook, Johanna C, Møller, Daniel V, Bundgaard, Henning, Christiansen, Michael
Publicado em 2013

MT-CYB mutations in hypertrophic cardiomyopathy

por Hagen, Christian M, Aidt, Frederik H, Havndrup, Ole, Hedley, Paula L, Jespersgaard, Cathrine, Jensen, Morten, Kanters, Jørgen K, Moolman-Smook, Johanna C, Møller, Daniel V, Bundgaard, Henning, Christiansen, Michael
Publicado em 2013

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

por Nyegaard, Mette, Overgaard, Michael T., Søndergaard, Mads T., Vranas, Marta, Behr, Elijah R., Hildebrandt, Lasse L., Lund, Jacob, Hedley, Paula L., Camm, A. John, Wettrell, Göran, Fosdal, Inger, Christiansen, Michael, Børglum, Anders D.
Publicado em 2012

A comprehensive analysis of nuclear-encoded mitochondrial genes in schizophrenia

por Gonçalves, Vanessa F, Cappi, Carolina, Hagen, Christian M, Sequeira, Adolfo, Vawter, Marquis P, Derkach, Andriy, Zai, Clement C, Hedley, Paula L, Bybjerg-Grauholm, Jonas, Pouget, Jennie G, Cuperfain, Ari B., Sullivan, Patrick F, Christiansen, Michael, Kennedy, James L, Sun, Lei
Publicado no Biol Psychiatry (2018)

Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease

por Hagen, Christian M., Gonçalves, Vanessa F., Hedley, Paula L., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Hansen, Christine S., Kanters, Jørgen K., Nielsen, Jimmi, Mors, Ole, Demur, Alfonso B., Als, Thomas D., Nordentoft, Merete, Børglum, Anders, Mortensen, Preben B., Kennedy, James, Werge, Thomas M., Hougaard, David M., Christiansen, Michael
Publicado no PLoS One (2018)

Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes

por Bybjerg-Grauholm, Jonas, Hagen, Christian M., Gonçalves, Vanessa F., Bækvad-Hansen, Marie, Hansen, Christine S., Hedley, Paula L., Kanters, Jørgen K., Nielsen, Jimmi, Theisen, Michael, Mors, Ole, Kennedy, James, Als, Thomas D., Demur, Alfonso B., Nordentoft, Merete, Børglum, Anders, Mortensen, Preben B., Werge, Thomas M., Hougaard, David M., Christiansen, Michael
Publicado no PLoS One (2018)

Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy

por Raju, Hariharan, Ware, James S., Skinner, Jonathan R., Hedley, Paula L., Arno, Gavin, Love, Donald R., van der Werf, Christian, Tfelt-Hansen, Jacob, Winkel, Bo Gregers, Cohen, Marta C., Li, Xinzhong, John, Shibu, Sharma, Sanjay, Jeffery, Steve, Wilde, Arthur A. M., Christiansen, Michael, Sheppard, Mary N., Behr, Elijah R.
Publicado no BMC Cardiovasc Disord (2019)

Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2

por Christiansen, Michael, Hedley, Paula L, Theilade, Juliane, Stoevring, Birgitte, Leren, Trond P, Eschen, Ole, Sørensen, Karina M, Tybjærg-Hansen, Anne, Ousager, Lilian B, Pedersen, Lisbeth N, Frikke-Schmidt, Ruth, Aidt, Frederik H, Hansen, Michael G, Hansen, Jim, Bloch Thomsen, Poul E, Toft, Egon, Henriksen, Finn L, Bundgaard, Henning, Jensen, Henrik K, Kanters, Jørgen K
Publicado em 2014