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Hansen-Kiss, Emily
57
results:
Search for persons
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Online (57)
Mediatypes
Articles (Online) (47)
Bookchapter (Online) (3)
OpenAccess-fulltext (7)
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?
1
Phenotypic Spectrum in a Family Sharing a Heterozygous KCNQ..:
Arredondo, Kristen
;
Myers, Cortlandt
;
Hansen-Kiss, Emily
...
Journal of Child Neurology. 37 (2022) 6 - p. 517-523 , 2022
Link:
https://doi.org/10.1177/..
?
2
Adams-Oliver Syndrome: Vestigial Tail and Genetics Update:
Zhu, Victor Z.
;
Hansen-Kiss, Emily
;
Hecht, Jacqueline T.
.
Archives of Plastic Surgery. 49 (2022) 4 - p. 517-522 , 2022
Link:
https://doi.org/10.1055/..
?
3
Pediatric Obstructive Sleep Medicine:
, In:
Dental Sleep Medicine
,
Wuertz, Karen
;
Glick, Aaron
;
Simmons, Jerald
. - p. 365-401 , 2022
Link:
https://doi.org/10.1007/..
?
4
CNTN6 copy number variations: Uncertain clinical significan..:
Repnikova, Elena A.
;
Lyalin, Dmitry A.
;
McDonald, Kimberly
...
European Journal of Medical Genetics. 63 (2020) 1 - p. 103636 , 2020
Link:
https://doi.org/10.1016/..
?
5
Testing Genetic Modifiers of Behavior and Response to Atomo..:
Barrie, Elizabeth S.
;
Pinsonneault, Julia K.
;
Sadee, Wolfgang
...
Journal of Developmental and Physical Disabilities. 30 (2018) 3 - p. 355-371 , 2018
Link:
https://doi.org/10.1007/..
?
6
Human CRMP4 mutation and disrupted Crmp4 expression in mice..:
Tsutiya, Atsuhiro
;
Nakano, Yui
;
Hansen-Kiss, Emily
...
Scientific Reports. 7 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
7
Rare coding variation provides insight into the genetic arc..:
Fu, Jack
;
Satterstrom, F. Kyle
;
Peng, Minshi
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41588-022-01104-0. , 2022
Link:
https://inserm.hal.scien..
?
8
Rare coding variation provides insight into the genetic arc..:
Fu, Jack M
;
Satterstrom, F Kyle
;
Peng, Minshi
...
qt04m356rr. , 2022
Link:
https://escholarship.org..
?
9
Rare coding variation provides insight into the genetic arc..:
Fu, Jack
;
Satterstrom, F. Kyle
;
Peng, Minshi
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41588-022-01104-0. , 2022
Link:
https://inserm.hal.scien..
?
10
Rare coding variation provides insight into the genetic arc..:
Fu, Jack
;
Satterstrom, F. Kyle
;
Peng, Minshi
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41588-022-01104-0. , 2022
Link:
https://inserm.hal.scien..
?
11
Large-Scale Exome Sequencing Study Implicates Both Developm..:
Satterstrom, F Kyle
;
Kosmicki, Jack A
;
Wang, Jiebiao
...
qt9bc7z9nn. , 2020
Link:
https://escholarship.org..
?
12
Large-Scale Exome Sequencing Study Implicates Both Developm..:
Satterstrom, F Kyle
;
Kosmicki, Jack A
;
Wang, Jiebiao
...
qt3gk8w6xr. , 2020
Link:
https://escholarship.org..
?
13
Adams-Oliver Syndrome: Vestigial Tail and Genetics Update:
Victor Z. Zhu
;
Emily Hansen-Kiss
;
Jacqueline T. Hecht
.
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0042-1751107. , 2022
Link:
https://doi.org/10.1055/..
?
14
A Counterion‐Directed Approach to the Diels–Alder Paradigm:..:
Kiss, Emily
;
Campbell, Craig D.
;
Driver, Russell W.
...
Angewandte Chemie. 128 (2016) 44 - p. 14017-14021 , 2016
Link:
https://doi.org/10.1002/..
?
15
A Counterion‐Directed Approach to the Diels–Alder Paradigm:..:
Kiss, Emily
;
Campbell, Craig D.
;
Driver, Russell W.
...
Angewandte Chemie International Edition. 55 (2016) 44 - p. 13813-13817 , 2016
Link:
https://doi.org/10.1002/..
1-15