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21篇 您的检索式：作者名="Bilguvar"

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	题名	作者	年代	出处	被引量
1	Susceptibility loci for intracranial aneurysm in European and Japanese populations 显示文摘	Bilguvar K Yasuno K Niemela M	2008	Nat Genet2008，40，12：	1
2	Genome-wide association study of intracranial aneurysm identifies three new risk loci显示文摘	Yasuno K Bilguvar K Bijlenga P	2010	Nat Genet2010，42，5：	1
3	Genome-wide association study of intracranial aneurysm identifies three new risk loci显示文摘	Yasuno K Bilguvar K Bijlenga P	2010	Nat Genet2010，42，：	1
4	Genome-wideassociation study of intracranial aneurysm identifiesthree new risk loci 显示文摘	Yasuno K Bilguvar K Bijlenga P	2010	Nat Genet2010，42，5：	1
5	Susceptibility loci for intracranial aneurysm in European and Japanese popu- lations显示文摘	Bilguvar K Yasuno K Niemela M	2008	Nature Genet2008，40，12：	1
6	Susceptibility loci for in- tracranial aneurysm in European and Japanese populations 显示文摘	Bilguvar K Yasuno K Niemela M	2008	Nature genetics2008，40，12：	1
7	Somatic V600E BRAF mutation in linear and sporadic syringocystadenoma papilliferum 显示文摘	Levinsohn JL Sugarman JL Bilguvar K	2015	J Invest Dermatol2015，135，10：	1
8	Genome-wide association study of intracranial aneurysm identifies three new risk loci显示文摘	Yasuno K Bilguvar K Bijlenga P	2010	Nat Genet2010，42，42：	1
9	Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism显示文摘	Stephan J. Sanders A. Gulhan Ercan-Sencicek Vanessa Hus Rui Luo Michael T. Murtha Daniel Moreno-De-Luca Su H. Chu Michael P. Moreau Abha R. Gupta Susanne A. Thomson Christopher E. Mason Kaya Bilguvar Patricia B.S. Celestino-Soper Murim Choi Emily L. Crawf	2011	Neuron2011，，5：	1
10	Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations 显示文摘	Bilguvar K Ozturk AK Louvi A	2010	Nature2010，467，7312：	1
11	Whole - exome sequencing identifies recessive WDR62 mutations in severe brain malformations 显示文摘	Bilguvar K Ozturk AK Louvi A	2010	Nature2010，467，7312：	1
12	Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations显示文摘	Bilguvar K Ozturk AK Louvi A		0，，9：	1
13	Whole exome sequencing identifies recessive WDR62 mutations in severe brain malformations显示文摘	Bilguvar K Oztiirk AK Louvi A	2010	Nature2010，467，7312：	1
14	Whole-exomesequencing identifies recessive WDR62 mutations in severebrain malformations显示文摘	Bilguvar K Oztiirk A K Louvi A	2010	Nature2010，467，7312：	1
15	Susceptibility loci for in- tracranial aneurysm in European and Japanese populations 显示文摘	Bilguvar K Yasuno K Niemela M	2008	Nat Genet2008，40，12：	1
16	Susceptibility loci for intracranial aneurysm in European and Japanese populations显示文摘	Bilguvar K Yasuno K Niemela M	2008	Nat Genet2008，40，：	1
17	Susceptibility loci for intracranial aneurysm in European and Japanese populations显示文摘	Bilguvar K Yasuno K Niemela M	2008	Nat Genet2008，40，12：	1
18	Susceptibility loci for intracranial aneurysm in European and Japanese populations显示文摘	Bilguvar K Yasuno K Niemela M		0，，12：	1
19	Whole-ex- ome-sequencing identifies recessive WDR62 mutations in severe brain malformations 显示文摘	Bilguvar K Ozttirk A K Louvi A	2010	Nature2010，467，7312：	1
20	COL4A1 mutationin preterm intraventricular hemorrhage显示文摘	Bilguvar K DiLuna ML Bizzarro MJ	2009	J Pediatr2009，155，5：	1

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