研究兴趣

论文共 106 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
时间
引用量
主题
期刊级别
合作者
合作机构
Long-read genome sequencing and RNA sequencing resolve an intronic LINE-1 insertion in the APC gene in a so far unsolved adenomatous polyposis family
Alexandra A. Baumann, Lisanne Knol, Marie Arlt, Tim Hutschenreiter, Anja Richter, Marcus Franke,Doreen William,Karl Hackmann,Daniela Richter,Isabel Spier,Stefan Aretz,Hanno Glimm,Evelin Schroeck,Arne Jahn
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 550-551
引用0浏览0引用
0
0
Limitations in Next-Generation Sequencing-Based Genotyping of Breast Cancer Polygenic Risk Score Loci
Alexandra Baumann,Christian Ruckert, Christoph Meier, Tim Hutschenreiter,Robert Remy, Benedikt Schnur, Marvin Doebel, Rudel Christian Nkouamedjo Fankep,Dariush Skowronek, Oliver Kutz,Norbert Arnold, Anna-Lena Katzke,Michael Forster, Anna-Lena Kobiela, Katharina Thiedig,Andreas Zimmer,Julia Ritter,Bernhard H. F. Weber,Ellen Honisch,Karl Hackmann,Gunnar Schmidt,Marc Sturm,Corinna Ernst, Marvin Dobel,Stephan Drukewitz,Christoph Engel,Peter Frommolt,Eva Gross,Johannes Helmuth, Zarah Kowalzyk,Maximilian Radtke,Juliane Ramser, Steffen Uebe,Shan Wang-Gohrke
EUROPEAN JOURNAL OF HUMAN GENETICSno. 8 (2024): 987-997
引用0浏览0WOSNATURE引用
0
0
An inherited PUF60 variant expands the genetic and phenotypic spectrum of the Verheij syndrome
Maria Constanza Roa Bravo, Andrea Kuebler,Karl Hackmann,Evelin Schroeck,Jens Schallner,Joseph Porrmann,Arne Jahn
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 542-542
引用0浏览0引用
0
0
Single Center Experience with Diagnostic Whole Genome Sequencing in 70 Patients with Rare Diseases
Doreen William, Zarah Kowalzyk,Karl Hackmann, Marion Bermudez, Oliver Kutz, Samira Zarvandi,Jan Fischer, Arne Jahn, Marcus Franke, Maria Constanza Roa Bravo, Lydia Rossow, Ann-Selin Onuk, Sylvia Huetter,Joseph Porrmann,Jens Schallner,Tanita Kretschmer, Catharina Schuetz, Min Ae Lee-Kirsch,Reinhard Berner,Evelin Schroeck, Nataliya Di Donato
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 292-292
引用0浏览0引用
0
0
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry
Martine Dumont,Nana Weber-Lassalle,Charles Joly-Beauparlant,Corinna Ernst,Arnaud Droit,Bing-Jian Feng,Stephane Dubois, Annie-Claude Collin-Deschesnes,Penny Soucy,Maxime Vallee,Frederic Fournier,Audrey Lemacon,Muriel A. Adank,Jamie Allen,Janine Altmueller,Norbert Arnold,Margreet G. E. M. Ausems,Riccardo Berutti,Manjeet K. Bolla,Shelley Bull,Sara Carvalho,Sten Cornelissen,Michael R. Dufault,Alison M. Dunning,Christoph Engel,Andrea Gehrig,Willemina R. R. Geurts-Giele,Christian Gieger,Jessica Green,Karl Hackmann,Mohamed Helmy,Julia Hentschel,Frans B. L. Hogervorst,Antoinette Hollestelle,Maartje J. Hooning,Judit Horvath,M. Arf An Ikram,Silke Kaulfuss,Renske Keeman,Da Kuang,Craig Luccarini,Wolfgang Maier,John W. M. Martens,Dieter Niederacher,Peter Nurnberg,Claus-Eric Ott,Annette Peters,Paul D. P. Pharoah,Alfredo Ramirez,Juliane Ramser,Steffi Riedel-Heller,Gunnar Schmidt,Mitul Shah,Martin Scherer, Antje Stabler,Tim M. Strom,Christian Sutter,Holger Thiele,Christi J. van Asperen,Lizet van der Kolk,Rob B. van der Luijt,Alexander E. Volk,Michael Wagner,Quinten Waisfisz,Qin Wang,Shan Wang-Gohrke,Bernhard H. F. Weber,Peter Devilee,Sean Tavtigian,Gary D. Bader,Alfons Meindl,David E. Goldgar,Irene L. Andrulis,Rita K. Schmutzler,Douglas F. Easton,Marjanka K. Schmidt,Eric Hahnen,Jacques Simard
Cancers（2022）
引用3浏览0WOS引用
3
0
加载更多
作者统计

#Papers: 106

#Citation: 2337

H-Index: 25

G-Index: 46

Sociability: 7

Diversity: 3

Activity: 5

  • 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