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Human Molecular Genetics
|
September 26, 2009
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate
Lina M Moreno, Maria Adela Mansilla, Steve A Bullard, et al.
Genetic Epidemiology
|
May 28, 2011
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate
Terri H Beaty, Ingo Ruczinski, Jeffrey C Murray, et al.
Nature Genetics
|
August 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency
Asmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, et al.
Nature Genetics
|
May 4, 2010
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
Terri H Beaty, Jeffrey C Murray, Mary L Marazita, et al.
Environmental Health Perspectives
|
July 10, 2026
Prenatal Smoking Exposures and Epigenome-Wide Methylation in Newborn Blood
Thanh T Hoang, Marta Cosin-Tomas, Yunsung Lee, et al.
Environmental Health Perspectives
|
June 6, 2025
Prenatal Smoking Exposures and Epigenome-wide Methylation in Newborn Blood
Thanh T Hoang, Marta Cosin-Tomas, Yunsung Lee, et al.
Nature Genetics
|
October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura
Gyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.
American Journal of Human Genetics
|
March 29, 2016
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
Elizabeth J Leslie, Huan Liu, Jenna C Carlson, et al.
Human Molecular Genetics
|
April 2, 2016
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13
Elizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Nature Communications
|
June 10, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
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of 10
Search research articles
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Showing results (81-90 of 93) with videos related to
Sort By:
Page
of 10
Human Molecular Genetics
|
September 26, 2009
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate
Lina M Moreno, Maria Adela Mansilla, Steve A Bullard, et al.
Genetic Epidemiology
|
May 28, 2011
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate
Terri H Beaty, Ingo Ruczinski, Jeffrey C Murray, et al.
Nature Genetics
|
August 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency
Asmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, et al.
Nature Genetics
|
May 4, 2010
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
Terri H Beaty, Jeffrey C Murray, Mary L Marazita, et al.
Environmental Health Perspectives
|
July 10, 2026
Prenatal Smoking Exposures and Epigenome-Wide Methylation in Newborn Blood
Thanh T Hoang, Marta Cosin-Tomas, Yunsung Lee, et al.
Environmental Health Perspectives
|
June 6, 2025
Prenatal Smoking Exposures and Epigenome-wide Methylation in Newborn Blood
Thanh T Hoang, Marta Cosin-Tomas, Yunsung Lee, et al.
Nature Genetics
|
October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura
Gyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.
American Journal of Human Genetics
|
March 29, 2016
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
Elizabeth J Leslie, Huan Liu, Jenna C Carlson, et al.
Human Molecular Genetics
|
April 2, 2016
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13
Elizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Nature Communications
|
June 10, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
Page
of 10