Completeness: 41 (100%)
Cited: 1 (1.47%)
All atributes instances: 41 (8.93%)
Identification (url, isbn, doi, issn, jstor, pmc, pmid, arxiv, oclc, website): 3 (100%)
Filled attributes and number of instances
title
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
1
date
9 September 2010
1
last2
Öztürk
1
last3
Louvi
1
last4
Kwan
1
last5
Choi
1
last6
Tatlı
1
last7
Yalnızoğlu
1
last8
Tüysüz
1
last9
Çağlayan
1
author
Bilgüvar K, Oztürk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnizoğlu D, Tüysüz B, Cağlayan AO, Gökben S, Kaymakçalan H, Barak T, Bakircioğlu M, Yasuno K, Ho W, Sanders S, Zhu Y, Yilmaz S, Dinçer A, Johnson MH, Bronen RA, Koçer N, Per H, Mane S, Pamir MN, Yalçinkaya C, Kumandaş S, Topçu M, Ozmen M, Sestan N, Lifton RP, State MW, Günel M
1
pages
207–210
1
journal
Nature
1
volume
467
1
issue
7312
1
doi
10.1038/nature09327
1
last20
Johnson
1
last21
Bronen
1
last22
Koçer
1
last23
Per
1
last24
Mane
1
last25
Pamir
1
last26
Yalçinkaya
1
last27
Kumandaş
1
last28
Topçu
1
last29
Ozmen
1
pmc
3129007
1
bibcode
2010Natur.467..207B
1
pmid
20729831
1
last15
Ho
1
last14
Yasuno
1
last17
Zhu
1
last16
Sanders
1
last11
Kaymakçalan
1
last10
Gökben
1
last13
Bakircioğlu
1
last12
Barak
1
last19
Dinçer
1
last18
Yilmaz
1
display-authors
8
1
last30
Sestan
1
Points based on comparison of each characteristics of the source with a median of each relevant characteristics of the TOP1000 corresponding sources In Russian Wikipedia:
| Characteristics | Median* |
|---|---|
| Completeness | 25 |
| Cited | 68 |
| All atributes instances | 459 |
* - as of August 2016
