I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Cornejo-Sanchez, Diana M
~ 200
results:
Search for persons
X
Format
Online
Mediatypes
Articles (Online)
Bookchapter (Online)
OpenAccess-fulltext
Languages
english (133)
spanish (23)
Sorted by: Relevance
Sorted by: Year
?
1
The genetic contribution of the X chromosome in age-related..:
Naderi, Elnaz
;
Cornejo-Sanchez, Diana M.
;
Li, Guangyou
...
Frontiers in Genetics. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
2
Rare-variant association analysis reveals known and new age..:
Cornejo-Sanchez, Diana M.
;
Li, Guangyou
;
Fabiha, Tabassum
...
European Journal of Human Genetics. 31 (2023) 6 - p. 638-647 , 2023
Link:
https://doi.org/10.1038/..
?
3
Variants in JAZF1 are associated with asthma, type 2 diabet..:
DeWan, Andrew T.
;
Cahill, Megan E.
;
Cornejo-Sanchez, Diana M.
...
Frontiers in Genetics. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
4
SCN1A Variants as the Underlying Cause of Genetic Epilepsy ..:
Cornejo-Sanchez, Diana M.
;
Acharya, Anushree
;
Bharadwaj, Thashi
...
Genes. 13 (2022) 5 - p. 754 , 2022
Link:
https://doi.org/10.3390/..
?
5
Exome sequencing reveals predominantly de novo variants in ..:
Järvelä, Irma
;
Määttä, Tuomo
;
Acharya, Anushree
...
Human Genetics. 140 (2021) 7 - p. 1011-1029 , 2021
Link:
https://doi.org/10.1007/..
?
6
Sleepwalking and Sleep Paralysis: Prevalence in Colombian F..:
Cornejo-Sanchez, Diana M.
;
Carrizosa-Moog, Jaime
;
Cabrera-Hemer, Dagoberto
...
Journal of Child Neurology. 34 (2019) 9 - p. 491-498 , 2019
Link:
https://doi.org/10.1177/..
?
7
Hearing impairment locus heterogeneity and identification o..:
Schrauwen, Isabelle
;
Melegh, Béla I.
;
Chakchouk, Imen
...
European Journal of Human Genetics. 27 (2019) 6 - p. 869-878 , 2019
Link:
https://doi.org/10.1038/..
?
8
Variants in JAZF1 are associated with asthma, type 2 diabet..:
DeWan, Andrew T
;
Cahill, Megan E
;
Cornejo-Sanchez, Diana M
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291233/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
9
The genetic contribution of the X chromosome in age-related..:
Naderi, Elnaz
;
Cornejo-Sanchez, Diana M
;
Li, Guangyou
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988903/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
10
Exome sequencing of families from Ghana reveals known and c..:
Wonkam, Ambroise
;
Adadey, Samuel Mawuli
;
Schrauwen, Isabelle
...
Communications Biology. 5 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
11
Exome sequencing reveals predominantly de novo variants in ..:
Järvelä, Irma
;
Määttä, Tuomo
;
Acharya, Anushree
...
10.1007/s00439-021-02268-1. , 2022
Link:
http://hdl.handle.net/10..
?
12
Exome sequencing reveals predominantly de novo variants in ..:
Järvelä, Irma
;
Määttä, Tuomo
;
Acharya, Anushree
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197721/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
13
Exome sequencing reveals predominantly de novo variants in ..:
Järvelä, Irma
;
Määttä, Tuomo
;
Acharya, Anushree
...
HUMAN GENETICS. , 2021
Link:
https://trepo.tuni.fi/ha..
?
14
Exome sequencing reveals predominantly de novo variants in ..:
Järvelä, I. (Irma)
;
Määttä, T. (Tuomo)
;
Acharya, A. (Anushree)
... , 2021
Link:
http://urn.fi/urn:nbn:fi..
?
15
Hearing impairment locus heterogeneity and identification o..:
Schrauwen, Isabelle
;
Melegh, Béla I
;
Chakchouk, Imen
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6777543/. , 2019
Link:
http://www.ncbi.nlm.nih...
1-15