Lusine Nazaryan - University of Copenhagen

基本信息

浏览量：0

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 15 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Monoallelic Variation in DHX9, the Gene Encoding the DExH-box Helicase DHX9, Underlies Neurodevelopment Disorders and Charcot-Marie-Tooth Disease

Daniel G. Calame, Tianyu Guo,Chen Wang,Lillian Garrett,Angad Jolly,Moez Dawood,Alina Kurolap,Noa Zunz Henig,Jawid M. Fatih,Isabella Herman,Haowei Du,Tadahiro Mitani,Lore Becker,Birgit Rathkolb,Raffaele Gerlini,Claudia Seisenberger,Susan Marschall,Jill Hunter,Amanda Gerard,Alexis Heidlebaugh,Thomas Challman,Rebecca C. Spillmann,Shalini N. Jhangiani,Zeynep Coban-Akdemir,Seema Lalani,Lingxiao Liu,Anya Revah-Politi,Alejandro Iglesias,Edwin Guzman,Evan Baugh,Nathalie Boddaert,Sophie Rondeau, Clothide Ormieres,Giulia Barcia,Queenie K. G. Tan,Sophie Isabelle Thiffault,Tomi Pastinen,Kazim Sheikh,Suur Biliciler,Davide Mei,Federico Melani,Vandana Shashi,Yuval Yaron,Mary Steele,Emma Wakeling,Elsebet Ostergaard,Lusine Nazaryan-Petersen,Francisca Millan,Teresa Santiago-Sim,Julien Thevenon,Ange-Line Bruel,Christel Thauvin-Robinet,Denny Popp,Konrad Platzer,Pawel Gawlinski,Wojciech Wiszniewski,Dana Marafi,Davut Pehlivan,Jennifer E. Posey,Richard A. Gibbs,Valerie Gailus-Durner,Renzo Guerrini,Helmut Fuchs,Martin Hrabe de Angelis,Sabine M. Hoelter,Hoi-Hung Cheung,Shen Gu,James R. Lupski

AMERICAN JOURNAL OF HUMAN GENETICS（2023）

引用2浏览0WOS引用

Added value of reanalysing whole exome- and whole genome sequencing data with an extended gene panel and structural variant calling in patients suspected of having primary immune deficiency

Sara Morup,Lusine Nazaryan-Petersen,Migle Gabrielaite,Joanne Reekie,Hanne V. Marquart,Hans Jakob Hartling,Rasmus Marvig,Terese L. Katzenstein,Tania N. Masmas,Jens D. Lundgren,Daniel D. Murray,Marie Helleberg,Line Borgwardt

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 436-437

引用0浏览0引用

A Novel DOCK2 Variant in Siblings with Severe Combined Immunodeficiency

Maria Anna Bruusgaard-Mouritsen,Tania Masmas,Line Borgwardt,Lusine Nazaryan-Petersen,Carsten Heilmann,Hans O. Madsen,Hanne Vibeke Marquart

SCANDINAVIAN JOURNAL OF IMMUNOLOGYno. 3 (2023)

引用0浏览0引用

Identification and Analysis of Deletion Breakpoints in Four Mohr-Tranebjærg Syndrome (MTS) Patients

Nanna Dahl Rendtorff,Helena Gásdal Karstensen,Marianne Lodahl,John Tolmie,Catherine McWilliam,Mads Bak,Niels Tommerup,Lusine Nazaryan-Petersen,Henricus Kunst,Melanie Wong,Shelagh Joss,Valerio Carelli,Lisbeth Tranebjærg

Scientific reports（2022）

引用1浏览0WOSNATURE引用

Added Value of Reanalysis of Whole Exome- and Whole Genome Sequencing Data from Patients Suspected of Primary Immune Deficiency Using an Extended Gene Panel and Structural Variation Calling

Sara Bohnstedt Morup,Lusine Nazaryan-Petersen,Migle Gabrielaite,Joanne Reekie,Hanne Marquart,Hans Jakob Hartling,Rasmus L. Marvig,Terese L. Katzenstein,Tania N. Masmas,Jens Lundgren,Daniel D. Murray,Marie Helleberg,Line Borgwardt

Frontiers in immunology（2022）

引用3浏览0WOS引用

Chromothripsis and DNA Repair Disorders

Lusine Nazaryan-Petersen,Victoria Alexandra Bjerregaard,Finn Cilius Nielsen,Niels Tommerup,Zeynep Tuemer

JOURNAL OF CLINICAL MEDICINEno. 3 (2020): 613

引用17浏览0WOS引用

Multigenic Truncation of the Semaphorin-Plexin Pathway by a Germline Chromothriptic Rearrangement Associated with Moebius Syndrome

Lusine Nazaryan-Petersen, Ines R. Oliveira,Mana M. Mehrjouy,Juan M. M. Mendez,Mads Bak,Merete Bugge,Vera M. Kalscheuer,Iben Bache,Dustin C. Hancks,Niels Tommerup

Human mutation（2019）

引用5浏览0WOS引用

Haploinsufficiency of ARHGAP42 is associated with hypertension

Amanda S. Fjorder,Malene B. Rasmussen,Mana M. Mehrjouy,Lusine Nazaryan-Petersen,Claus Hansen,Mads Bak,Niels Grarup,Anne Nørremølle,Lars A. Larsen,Henrik Vestergaard,Torben Hansen,Niels Tommerup,Iben Bache

EUROPEAN JOURNAL OF HUMAN GENETICS（2019）

引用11浏览0WOSNATURE引用

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn