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Co-authors
(47)
Douglas L. Riegert-Johnson
3
Timothy W. Hefferon
3
Lisa A. Boardman
2
Gabriele Richard
2
Lance Williams
1
Journals
(8)
GENET MED
1
Heart Rhythm
1
J AMER COLL CARDIOL
1
BIOMED MATER
1
AM J MED GENET PART A
1
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Authors
Daniela Macaya
Daniela Macaya,Harvard University,Genetics & Genealogy,Cardiology,Molecular Biology
Edit
Daniela Macaya
Harvard University
Publications:
8
|
Citations:
29
Fields:
Genetics & Genealogy
,
Cardiology
,
Molecular Biology
View FAQ about top research areas and Fields of study
Collaborated with
47 co-authors
from 2007 to 2012
|
Cited by
132 authors
Cumulative
Annual
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Publications
(8)
BibTeX
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RIS
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RefWorks
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Injectable hydrogel materials for spinal cord regeneration: a review
D Macaya
,
M Spector
Journal:
Biomedical Materials - BIOMED MATER
, vol. 7, no. 1, 2012
GENETIC TESTING PANELS AS AN AID TO DIAGNOSIS OF HERITABLE DILATED CARDIOMYOPATHY
Amy Daly
,
Daniela Macaya
,
Leah Betman
,
Kristin Van Goor
,
Shruti Mitkus
,
Wendy Chung
,
Gabriele Richard
Journal:
Journal of The American College of Cardiology - J AMER COLL CARDIOL
, vol. 57, no. 14, pp. E2042-E2042, 2011
Result of Genetic Testing in 856 Consecutive Unrelated Patients Referred for Long QT Syndrome in a Clinical Laboratory
K. V. V. Lieve
,
L. Williams
,
A. Daly
,
G. Richard
,
S. Bale
,
D. Macaya
,
W. Chung
Journal:
Heart Rhythm
, vol. 8, no. 11, pp. 1826-1826, 2011
Mutations in Fibrillin1 Cause Congenital Scleroderma: Stiff Skin Syndrome
(
Citations: 13
)
B. L. Loeys
,
E. E. Gerber
,
D. Riegert-Johnson
,
S. Iqbal
,
P. Whiteman
,
V. McConnell
,
C. R. Chillakuri
,
D. Macaya
,
P. J. Coucke
,
A. De Paepe
,
D. P. Judge
,
F. Wigley
http://academic.research.microsoft.com/io.ashx?type=5&id=25116927&selfId1=26832578&selfId2=0&maxNumber=12&query=
Journal:
Science Translational Medicine
, vol. 2, no. 23, pp. 23ra20-23ra20, 2010
Newborn screening for X-linked adrenoleukodystrophy (X-ALD): Validation of a combined liquid chromatography–tandem mass spectrometric (LC–MS/MS) method
(
Citations: 12
)
Walter C. Hubbard
,
Ann B. Moser
,
Anita C. Liu
,
Richard O. Jones
,
Steven J. Steinberg
,
Fred Lorey
,
Susan R. Panny
,
Robert F. Vogt Jr.
,
Daniela Macaya
,
Coleman T. Turgeon
,
Silvia Tortorelli
,
Gerald V. Raymond
Journal:
Molecular Genetics and Metabolism - MOL GENET METAB
, vol. 97, no. 3, pp. 212-220, 2009
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Citations
(29 times by 29 publications)
Microenvironmental Regulation by Fibrillin1
Gerhard Sengle
,
Ko Tsutsui
,
Douglas R. Keene
,
Sara F. Tufa
,
Eric J. Carlson
,
Noe L. Charbonneau
,
Robert N. Ono
,
Takako Sasaki
,
Mary K. Wirtz
,
John R. Samples
,
Liselotte I. Fessler
,
John H. Fessler
http://academic.research.microsoft.com/io.ashx?type=5&id=57409680&selfId1=26832578&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 1, 2012
Bezafibrate for X-Linked Adrenoleukodystrophy
Marc Engelen
,
Luc Tran
,
Rob Ofman
,
Josephine Brennecke
,
Ann B. Moser
,
Inge M. E. Dijkstra
,
Ronald J. A. Wanders
,
Bwee Tien Poll-The
,
Stephan Kemp
Journal:
PLOS One
, vol. 7, no. 7, 2012
The Evolution of Extracellular Fibrillins and Their Functional Domains
Adam Piha-Gossack
,
Wayne Sossin
,
Dieter P. Reinhardt
Journal:
PLOS One
, vol. 7, no. 3, 2012
Characterisation and removal of recalcitrants in reverse osmosis concentrates from water reclamation plants
(
Citations: 1
)
Arseto Y. Bagastyo
,
Jurg Keller
,
Yvan Poussade
,
Damien J. Batstone
Journal:
Water Research - WATER RES
, vol. 45, no. 7, pp. 2415-2427, 2011
Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome
Carine Le Goff
,
Clémentine Mahaut
,
Avinash Abhyankar
,
Wilfried Le Goff
,
Valérie Serre
,
Alexandra Afenjar
,
Anne Destrée
,
Maja di Rocco
,
Delphine Héron
,
Sébastien Jacquemont
,
Sandrine Marlin
,
Marleen Simon
http://academic.research.microsoft.com/io.ashx?type=5&id=56593526&selfId1=26832578&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 44, no. 1, pp. 85-88, 2011
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