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	题名	作者	年代	出处	被引量
1	ACEpolymorphisms显示文摘	Sayed-Tabatabaei FA Oostra BA Isaacs A		0，，09：	1
2	Studying the genetics of Hirschsprung's disease:unraveling an oligogenic disorder显示文摘	Brooks AS Oostra BA Hofstra RM	2005	Clin Genet2005，67，：	1
3	Diagnosis and localization of a complicated urinary tract infection in neurogenic bladder disease by tubular pro teinuria and serum prostate specific antigen显示文摘	Oostra C Delanghe J	1998	Spinal Cord1998，36，1：	1
4	A perfusion bioreactor system capable of producing clinically relevant volumes of tissue-engineered bone: in vivo bone formation showing proof of concept 显示文摘	Janssen F W Oostra J Oorschot A	2006	Biomaterials2006，27，3：	1
5	Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome 显示文摘	Restivo L Ferrari F Passino E Sgobio C Bock J Oostra BA	2005	Proc Natl Acad Sci USA2005，102，11：	1
6	A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan显示文摘	Alessio Fonzo Yah-Huei Wu-Chou Chin-Song Lu Marina Doeselaar Erik J. Simons Christan F. Rohé Hsiu-Chen Chang Rou-Shayn Chen Yi-Hsin Weng Nicola Vanacore Guido J. Breedveld Ben A. Oostra Vincenzo Bonifati	2006	Neurogenetics2006，，3：	1
7	Insulin-resistance and metabolic syndrome are related to executive function in women in a large family-based study显示文摘	M. Schuur P. Henneman J. C. Swieten M. C. Zillikens I. Koning A. C. J. W. Janssens J. C. M. Witteman Y. S. Aulchenko R. R. Frants B. A. Oostra K. Willems Dijk C. M. Duijn	2010	European Journal of Epidemiology2010，，8：	1
8	The hemochromatosis N144H mutation of SLC11A3 gene in patients with type 2 diabetes显示文摘	NJAJOU O T VAESSEN N OOSTRA B	2002	Mol Genet Metab2002，75，：	1
9	Hybrid-rangier Locomotive:Technik und Anwendungen显示文摘	OOSTRA J DUNGER W	2009	ZEV Rail Glasers Annalen2009，133，9：	1
10	Role of trastuzumab emtansine in the treatmentof HER2-positive breast cancer显示文摘	Oostra DR Macrae ER	2014	Breast Cancer( Dove Med Press)2014，6，：	1
11	FMRP detection assay for the diagnosis of the fragile X syndrome 显示文摘	Willemsen R Oostra BA	2000	Am J Med Genet2000，97，3：	1
12	A fragile balance: FMR1 expression levels 显示文摘	Oostra BA Willemsen R	2003	Hum Mol Genet2003，，2：	1
13	Linking DJ-1 to neu-rodegeneration offers novel insights for understanding the patho-genesis of Parkinson's disease显示文摘	BONIFATI V OOSTRA BA HEUTINK P	2004	J Mol Med ( Berl)2004，82，3：	1
14	FMRP detection assay for the diagnosis of the Fragile X syndrome 显示文摘	Willemsen R Oostra B	2000	Am J Med Genet2000，97，4：	1
15	PARK6 is a common cause of familial parkinsonism显示文摘	E.M. Valente F. Brancati V. Caputo E.A. Graham M.B. Davis A. Ferraris M.M.B. Breteler T. Gasser V. Bonifati A.R. Bentivoglio G. De Michele A. Dürr P. Cortelli A. Filla G. Meco B.A. Oostra A. Brice A. Albanese B. Dallapiccola N.W. Wood	2002	Neurological Sciences2002，，2：	1
16	Linking DJ- 1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinsons disease显示文摘	Bonifati V Oostra BA Heutink P	2004	J Mol Med2004，82，：	1
17	Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype显示文摘	Joenje H Lo ten Foe JR Oostra AB	1995	Blood1995，86，6：	1
18	Segmen- tation anomalies of vertebrae and ribs with other abnor- malities of blastogenesis: syndromes or associations? 显示文摘	Gilbert-Barness E Oostra R J Agarwal A	2005	Fetal Pediatr Pathol2005，24，6：	1
19	Adolescents'perceptions of communication with parents relative to specific aspects of relationships with parents and personal development显示文摘	JACKSON S BIJSTRA J OOSTRA L	1998	J Adoles1998，21，3：	1
20	PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36显示文摘	C.M. van Duijn M.C.J. Dekker V. Bonifati R.J. Galjaard J.J. Houwing-Duistermaat P.J.L.M. Snijders L. Testers G.J. Breedveld M. Horstink L.A. Sandkuijl J.C. van Swieten B.A. Oostra P. Heutink	2001	The American Journal of Human Genetics2001，，3：	1

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