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Co-authors
(53)
Julie E. Hoover-Fong
3
Bart L. Loeys
3
David Valle
3
George D. H. Thomas
3
Harry C. Dietz
3
Journals
(6)
PLOS GENET
2
AMER J OBSTET GYNECOL
1
CARDIOVASC PATHOL
1
J BONE JOINT SURG-AMER VOL
1
N ENGL J MED
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Authors
Gretchen L. Oswald
Gretchen L. Oswald,Genetics & Genealogy,Cardiology,Diabetes
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Gretchen L. Oswald
Publications:
8
|
Citations:
208
Fields:
Genetics & Genealogy
,
Cardiology
,
Diabetes
View FAQ about top research areas and Fields of study
Collaborated with
53 co-authors
from 2004 to 2011
|
Cited by
1044 authors
Cumulative
Annual
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Publications
(8)
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RefWorks
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Causes and histopathology of ascending aortic disease in children and young adults
(
Citations: 3
)
Deepali Jain
,
Harry C. Dietz
,
Gretchen L. Oswald
,
Joseph J. Maleszewski
,
Marc K. Halushka
Journal:
Cardiovascular Pathology - CARDIOVASC PATHOL
, vol. 20, no. 1, pp. 15-25, 2011
Whole-Genome Sequencing of a Single Proband Together with Linkage Analysis Identifies a Mendelian Disease Gene
(
Citations: 18
)
Nara L. M. Sobreira
,
Elizabeth T. Cirulli
,
Dimitrios Avramopoulos
,
Elizabeth Wohler
,
Gretchen L. Oswald
,
Eric L. Stevens
,
Dongliang Ge
,
Kevin V. Shianna
,
Jason P. Smith
,
Jessica M. Maia
,
Curtis E. Gumbs
,
Jonathan Pevsner
http://academic.research.microsoft.com/io.ashx?type=5&id=38775709&selfId1=23941999&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 6, no. 6, 2010
Musculoskeletal Findings of Loeys-Dietz Syndrome
(
Citations: 2
)
G. Erkula
,
P. D. Sponseller
,
L. C. Paulsen
,
G. L. Oswald
,
B. L. Loeys
,
H. C. Dietz
Journal:
Journal of Bone and Joint Surgery-american Volume - J BONE JOINT SURG-AMER VOL
, vol. 92, no. 9, pp. 1876-1883, 2010
Whole-Genome Sequencing of a Single Proband Together with Linkage Analysis Identifies a Mendelian Disease Gene
Nara L. M. Sobreira
,
Elizabeth T. Cirulli
,
Dimitrios Avramopoulos
,
Elizabeth Wohler
,
Gretchen L. Oswald
,
Eric L. Stevens
,
Dongliang Ge
,
Kevin V. Shianna
,
Jason P. Smith
,
Jessica M. Maia
,
Curtis E. Gumbs
,
Jonathan Pevsner
http://academic.research.microsoft.com/io.ashx?type=5&id=57408835&selfId1=23941999&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 6, no. 6, 2010
Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor
(
Citations: 183
)
Bart L. Loeys
,
Ulrike Schwarze
,
Tammy Holm
,
Bert L. Callewaert
,
George H. Thomas
,
Hariyadarshi Pannu
,
Julie F. De Backer
,
Gretchen L. Oswald
,
Sofie Symoens
,
Sylvie Manouvrier
,
Amy E. Roberts
,
Francesca Faravelli
http://academic.research.microsoft.com/io.ashx?type=5&id=10111377&selfId1=23941999&selfId2=0&maxNumber=12&query=
Journal:
New England Journal of Medicine - N ENGL J MED
, vol. 355, no. 8, pp. 788-798, 2006
Sort by:
Citations
(208 times by 207 publications)
A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions
Kaja K Selmer
,
Gregor D Gilfillan
,
Petter Strømme
,
Robert Lyle
,
Timothy Hughes
,
Hanne S Hjorthaug
,
Kristin Brandal
,
Sigve Nakken
,
Doriana Misceo
,
Thore Egeland
,
Ludvig A Munthe
,
Sigrun K Braekken
http://academic.research.microsoft.com/io.ashx?type=5&id=56548410&selfId1=23941999&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 20, no. 1, pp. 58-63, 2012
Clinical features and genetic analysis of Korean patients with Loeys–Dietz syndrome
Jeong Hoon Yang
,
Chang-Seok Ki
,
Hyejin Han
,
Bong Gun Song
,
Shin Yi Jang
,
Tae-Young Chung
,
Kiick Sung
,
Heung Jae Lee
,
Duk-Kyung Kim
,
D-K Kim
,
HJ Lee
Journal:
Journal of Human Genetics - J HUM GENET
, vol. 57, no. 1, pp. 52-56, 2012
Statistical Guidance for Experimental Design and Data Analysis of Mutation Detection in Rare Monogenic Mendelian Diseases by Exome Sequencing
Degui Zhi
,
Rui Chen
Journal:
PLOS One
, vol. 7, no. 2, 2012
Revisiting Mendelian disorders through exome sequencing
(
Citations: 5
)
Chee-Seng Ku
,
Nasheen Naidoo
,
Yudi Pawitan
Journal:
Human Genetics - HUM GENET
, vol. 129, no. 4, pp. 351-370, 2011
Genome-wide analysis of Ollier disease: Is it all in the genes?
(
Citations: 3
)
Twinkal C Pansuriya
,
Jan Oosting
,
Tibor Krenács
,
Antonie HM Taminiau
,
Suzan HM Verdegaal
,
Luca Sangiorgi
,
Raf Sciot
,
Pancras CW Hogendoorn
,
Karoly Szuhai
,
Judith VMG Bovée
Journal:
Orphanet Journal of Rare Diseases - ORPHANET J RARE DIS
, vol. 6, no. 1, pp. 2-11, 2011
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