Weiter zum Inhalt
Toggle navigation
English
English
Favoritenliste (
0
)
(Voll)
Kontakt
Mein Konto
Abmeldung
Mein Konto
Suche
Erweiterte Suche
Suchverlauf
Struktursuche
Narrative Service
Drug Overviews
Info Guide
/vufind/Search/Results?lookfor=%22Klee%2C+Eric+W%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Klee%2C+Eric+W%22&type=Person&sort=year
Search /vufind/Search2/Results?lookfor=%22Klee%2C+Eric+W%22&type=Person&sort=year
PubPharm (380)
1
MARK2
variants cause autism spectrum disorder
via
the downregulation of WNT/β-catenin signaling pathway
enthalten in:
bioRxiv.org
| 2024
von
Gong, M.
|
Li, J.
|
Liu, Y.
| +63
Wird geladen...
2
Unified somatic calling and machine learning-based classification enhance the discovery of clonal hematopoiesis of indeterminate potential
enthalten in:
bioRxiv.org
| 2024
von
Tian, S.
|
Ferrer, A.
|
Yan, H.
| +10
Wird geladen...
3
Pathogenic
SPTBN1
variants cause a novel autosomal dominant neurodevelopmental syndrome
enthalten in:
bioRxiv.org
| 2024
von
Cousin, M.
|
Breau, K.
|
Creighton, B.
| +64
Wird geladen...
4
Genomic epidemiology reveals the dominance of Hennepin County in transmission of SARS-CoV-2 in Minnesota from 2020-2022
enthalten in:
bioRxiv.org
| 2024
von
Scotch, M.
|
Lauer, K.
|
Wieben, E.
| +17
Wird geladen...
5
Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger Syndrome
enthalten in:
American journal of medical genetics. Part A
| 2024
von
Farris, J.
|
Khanna, C.
|
Smadbeck, J.
| +14
Wird geladen...
6
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease
enthalten in:
BMC genomics
| 2024
von
Fadra, N.
|
Schultz-Rogers, L.
|
Chanana, P.
| +9
Wird geladen...
7
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease
enthalten in:
BMC genomics
| 2024
von
Fadra, N.
|
Schultz-Rogers, L.
|
Chanana, P.
| +9
Wird geladen...
8
OmicsFootPrint: a framework to integrate and interpret multi-omics data using circular images and deep neural networks
enthalten in:
bioRxiv.org
| 2024
von
Tang, X.
|
Prodduturi, N.
|
Thompson, K.
| +9
Wird geladen...
9
OmicsFootPrint : a framework to integrate and interpret multi-omics data using circular images and deep neural networks
enthalten in:
bioRxiv : the preprint server for biology
| 2024
von
Tang, X.
|
Prodduturi, N.
|
Thompson, K.
| +9
Wird geladen...
10
Semiautomated approach focused on new genomic information results in time and effort- efficient reannotation of negative exome data
enthalten in:
ResearchSquare.com
| 2024
von
Ferrer, A.
|
Duffy, P.
|
Olson, R.
| +25
Wird geladen...
1
2
3
4
5
6
7
8
9
10
11
Nächster »
[38]
Filter & Sortierung
Treffer pro Seite
10
20
50
Sortieren
Relevanz
Neueste zuerst
Älteste zuerst
Verfasser
Zeitschriftentitel
Bibliothek
Standort (Printmedien)
Verwandte Substanzen
Verwandte Substanzen werden ermittelt...
Verwandte Erkrankungen/Symptome
Verwandte Erkrankungen/Symptome werden ermittelt...
Verwandte Gene
Verwandte Gene werden ermittelt...
Systematic Reviews
Clinical Studies
Patente
Covid-19/SARS-CoV-2
Exclude Systematic Reviews
Exclude Clinical Studies
Exclude Patents
Medienart
380
Aufsätze
321
E-Artikel
321
E-Ressourcen
59
Gedruckte Aufsätze
Zeitschriftentitel
16
bioRxiv.org
15
Clinical chemistry
14
American journal of human genetics
13
BMC bioinformatics
12
Journal of clinical immunology
11
American journal of medical genetics. Part A
11
Genetics in medicine : official journal of the ...
10
Molecular genetics & genomic medicine
8
BMC genomics
8
Cold Spring Harbor molecular case studies
8
European journal of human genetics : EJHG
8
Mayo Clinic proceedings
7
American Journal of Medical Genetics Part C: Se...
6
BMC medical genetics
6
Human mutation
6
Molecular Genetics & Genomic Medicine
6
Nucleic acids research
5
Frontiers in genetics
5
PloS one
5
The Journal of molecular diagnostics : JMD
Alle anzeigen ...
weniger ...
Thema
199
Journal Article
118
Research Support, Non-U.S. Gov't
72
Research Support, N.I.H., Extramural
56
Case Reports
17
Review
11
Biomarkers, Tumor
11
DNA-Binding Proteins
11
intellectual disability
10
570
10
Letter
9
Biology
8
Transcription Factors
7
Comparative Study
7
EC 2.7.11.1
7
Individualized medicine
7
Nerve Tissue Proteins
7
RNA, Messenger
7
whole exome sequencing
6
63231-63-0
6
Biomarkers
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
151
2020-
191
2010-2019
36
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
327
Englisch
Haven't found what you're looking for?
Wird geladen...