ScholarIQanswers from OpenAlex & ORCID
Fabian Grubert
ResearcherPublications, citations & collaboration network
Fabian Grubert is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Fabian Grubert have?
ScholarIQindexed works
Fabian Grubert has 43 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Fabian Grubert have?
ScholarIQcitation count
Fabian Grubert has 46,534 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Fabian Grubert?
ScholarIQh-index
Fabian Grubert has an h-index of 32 in OpenAlex.
What is the i10-index of Fabian Grubert?
ScholarIQi10-index
Fabian Grubert has an i10-index of 36 in OpenAlex.
What is the OpenAlex record for Fabian Grubert?
ScholarIQopenalex
The OpenAlex for Fabian Grubert is on the source record.
What are the most-cited papers on Fabian Grubert?
ScholarIQmost cited works
Architecture of the human regulatory network derived from ENCODE data
Mark Gerstein, Anshul Kundaje, Manoj Hariharan, Stephen G. Landt, Koon‐Kiu Yan, Chao Cheng, Xinmeng Jasmine Mu, Ekta Khurana, Joel Rozowsky, Roger P. Alexander, Renqiang Min, Pedro Alves, Alexej Abyzov, Nick Addleman, Nitin Bhardwaj, Alan P. Boyle, Philip Cayting, Alexandra Charos, David Ziyou Chen, Yong Cheng, Declan Clarke, Catharine Eastman, Ghia Euskirchen, Seth Frietze, Yao Fu, Jason Gertz, Fabian Grubert, Arif Harmanci, Preti Jain, Maya Kasowski, Phil Lacroute, Jing Leng, Jin Lian, Hannah Monahan, Henriette O’Geen, Zhengqing Ouyang, E. Christopher Partridge, Dorrelyn Patacsil, Florencia Pauli, Debasish Raha, Lucı́a Ramı́rez, Timothy E. Reddy, Brian D. Reed, Minyi Shi, Teri Slifer, Jing Wang, Linfeng Wu, Xinqiong Yang, Kevin Y. Yip, Gili Zilberman-Schapira, Serafim Batzoglou, Arend Sidow, Peggy Farnham, R Myers, Sherman M. Weissman, M Snyder
Mapping copy number variation by population-scale genome sequencing
1000 Genomes Project, Ryan E. Mills, Klaudia Walter, Chip Stewart, Robert E. Handsaker, Ken Chen, Can Alkan, Alexej Abyzov, Seungtai Yoon, Kai Ye, R. Keira Cheetham, Asif Chinwalla, Donald F. Conrad, Yutao Fu, Fabian Grubert, Iman Hajirasouliha, Fereydoun Hormozdiari, Lilia M. Iakoucheva, Zamin Iqbal, Shuli Kang, Jeffrey M. Kidd, Miriam K. Konkel, Joshua M. Korn, Ekta Khurana, Deniz Kural, Hugo Y. K. Lam, Jing Leng, Ruiqiang Li, Yingrui Li, Chang‐Yun Lin, Ruibang Luo, Xinmeng Jasmine Mu, James Nemesh, Heather E. Peckham, Tobias Rausch, Aylwyn Scally, Xinghua Shi, Michael P. Strömberg, Adrian M. Stütz, Alexander E. Urban, Jerilyn A. Walker, Jiantao Wu, Yujun Zhang, Zhengdong D. Zhang, Mark A. Batzer, Li Ding, Gábor Marth, Gil McVean, Jonathan Sebat, M Snyder, Jun Wang, Kenny Ye, Evan E. Eichler, Mark Gerstein, Matthew E. Hurles, Charles Lee, Steven A. McCarroll, Jan O. Korbel
Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
Juliane Winkelmann, Ling Lin, Barbara Schormair, Birgitte Rahbek Kornum, Juliette Faraco, Giuseppe Plazzi, Atle Melberg, F. Cornelio, Alexander E. Urban, Fabio Pizza, Francesca Poli, Fabian Grubert, Thomas Wieland, Elisabeth Graf, Joachim Hallmayer, Tim M. Strom, Emmanuel Mignot