Peer reviewed reports at the center of my research

Earlier Report“2005 Report” 2005: Phenotype of Heterozygotes for Low-Density Lipoprotein Receptor Mutations Identified in Different Background Populations; Anne Tybjærg-Hansen, Henrik Kjærulf Jensen, Marianne Benn, Rolf Steffensen, Gorm Jensen, Børge G. NordestgaardDOI: 10.1161/01.ATV.0000149380.94984.f0
 “Dutch report on Founder Effect” “Kusters et al” 2011: Founder mutations in the Netherlands: geographical distribution of the most prevalent mutations in the low-density lipoprotein receptor and apolipoprotein B genes; D.Meeike Kusters, Roeland Huijgen; Joep C. Defesche; Maud N. Vissers, Iris Kindt, Barbara A. Hutten and John .J.P. Kastelein; Downloaded from UvA-DARE, the institutional repository of the University of Amsterdam (UvA) http://hdl.handle.net/11245/2.114966
“2011 report” “2011 JCL series” “report in the Journal of Clinical Lipidology”   2011: A series of reports, but the lead report is titled, Familial Hypercholesterolemia: Screening, diagnosis and management of pediatric and adult patients Clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia Anne C. Goldberg, MD, FNLA, Chair*, Paul N. Hopkins, MD, MSPH, Peter P. Toth, MD, PhD, FNLA, Christie M. Ballantyne, MD, FNLA, Daniel J. Rader, MD, FNLA, Jennifer G. Robinson, MD, MPH, FNLA, Stephen R. Daniels, MD, PhD, Samuel S. Gidding, MD, Sarah D. de Ferranti, MD, MPH, Matthew K. Ito, PharmD, FNLA, Mary P. McGowan, MD, FNLA, Patrick M. Moriarty, MD, William C. Cromwell, MD, FNLA, Joyce L. Ross, MSN, CRNP, FNLA, Paul E. Ziajka, MD, PhD, FNLA; doi:10.1016/j.jacl.2011.04.003 Other reports in this series: doi:10.1016/j.jacl.2011.03.452; doi:10.1016/j.jacl.2011.03.451; doi:10.1016/j.jacl.2011.03.453; doi:10.1016/j.jacl.2011.04.001; doi:10.1016/j.jacl.2011.04.002
“1st Danish Report” “2012 Danish report” 2012: Familial Hypercholesterolemia in the Danish General Population: Prevalence, Coronary Artery Disease, and Cholesterol-Lowering Medication: Marianne Benn, Gerald F. Watts, Anne Tybjaerg-Hansen, and Børge G. Nordestgaard J Clin Endocrin Metab. First published ahead of print August 14, 2012 as doi:10.1210/jc.2012-1563
“2013 EAS Report” “2013 Consensus Panel of Experts”  Authoritative Report” 2013: Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society: Børge G. Nordestgaard, M. John Chapman, Steve E. Humphries, Henry N. Ginsberg, Luis Masana, Olivier S. Descamps, Olov Wiklund, Robert A. Hegele, Frederick J. Raal, Joep C. Defesche, Albert Wiegman, Raul D. Santos, Gerald F. Watts, Klaus G. Parhofer, G. Kees Hovingh, Petri T . Kovanen, Catherine Boileau, Maurizio Averna, Jan Bore´n, Eric Bruckert, Alberico L. Catapano, Jan Albert Kuivenhoven, Pa¨ivi Pajukanta, Kausik Ray, Anton F. H. Stalenhoef, Erik Stroes, Marja-Riitta Taskinen, and Anne Tybjærg-Hansen, for the European Atherosclerosis Society Consensus Panel European Heart Journal doi:10.1093/eurheartj/eht273
“Dutch Report” 2014 Homozygous autosomal dominant hypercholesterolaemia in the Netherlands: prevalence, genotype–phenotype relationship, and clinical outcome: Barbara Sjouke, D. Meeike Kusters, Iris Kindt, Joost Besseling, Joep C. Defesche, Eric J.G. Sijbrands, Jeanine E. Roeters van Lennep, Anton F.H. Stalenhoef, Albert Wiegman, Jacqueline de Graaf, Sigrid W. Fouchier, John J.P. Kastelein, and G. Kees Hovingh doi:10.1093/eurheartj/ehu058
“2014 EAS Report” “2014 Consensus Panel of Experts” 2014 Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society: Marina Cuchel, Eric Bruckert, Henry N. Ginsberg, Frederick J. Raal, Raul D. Santos, Robert A. Hegele, Jan Albert Kuivenhoven, Børge G. Nordestgaard, Olivier S. Descamps, Elisabeth Steinhagen-Thiessen, Anne Tybjærg-Hansen, Gerald F. Watts, Maurizio Averna, Catherine Boileau, Jan Bore´ n, Alberico L. Catapano, Joep C. Defesche, G. Kees Hovingh, Steve E. Humphries, Petri T. Kovanen, Luis Masana, Pa¨ivi Pajukanta, Klaus G. Parhofer, Kausik K. Ray, Anton F. H. Stalenhoef, Erik Stroes,Marja-Riitta Taskinen, Albert Wiegman, Olov Wiklund, and M. John Chapman, for the European Atherosclerosis Society Consensus Panel on Familial Hypercholesterolaemia doi:10.1093/eurheartj/ehu274
“Corrigendum” (to 1st Report) 2014: Corrigendum to “Familial Hypercholesterolemia in the Danish General Population: Prevalence, Coronary Artery Disease, and Cholesterol-Lowering Medication” by Marianne Benn, Gerald F. Watts, Anne Tybjærg-Hansen, and Børge G. Nordestgaard jcem.endojournals.org J Clin Endocrinol Metab, December 2014, 99(12):4758–4759 doi: 10.1210/jc.2014-3926
“Doctor’s Dilemma” “Dr. Baum’s Language Strategy” 2014: The doctor’s dilemma: Challenges in the diagnosis and care of homozygous familial hypercholesterolemia: Seth J. Baum, MD;  https://doi.org/10.1016/j.jacl.2014.09.005
 “2nd Danish Report” “2016 Danish Report” 2016: Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217: Marianne Benn, Gerald F. Watts, Anne Tybjærg-Hansen, and Børge G. Nordestgaard (Note, this includes the supplementary material) 2016: Supplementary Material: How to identify persons with mutations causative for familial hypercholesterolemia: Screening of 98,098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217 European Heart Journal (2016) 37, 1384–1394 doi:10.1093/eurheartj/ehw028
“Regeneron report” 2016: Genetic identification of familial hypercholesterolemia within a single U.S. health care system: Noura S. Abul-Husn, Kandamurugu Manickam, Laney K. Jones, Eric A. Wright, Dustin N. Hartzel, Claudia Gonzaga-Jauregui, Colm O’Dushlaine, Joseph B. Leader, H. Lester Kirchner, D’Andra M. Lindbuchler, Marci L. Barr, Monica A. Giovanni, Marylyn D. Ritchie, John D. Overton, Jeffrey G. Reid, Raghu P. R. Metpally, Amr H. Wardeh, Ingrid B. Borecki, George D. Yancopoulos, Aris Baras, Alan R. Shuldiner, Omri Gottesman, David H. Ledbetter, David J. Carey, Frederick E. Dewey, Michael F. Murray  DOI: 10.1126/science.aaf7000