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Kwong, Alan
281  results:
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1

Genetic neurodevelopmental clustering and dyslexia:

Ciulkinyte, Austeja ; Mountford, Hayley S. ; Fontanillas, Pierre...
Molecular Psychiatry.  , 2024
Link: https://doi.org/10.1038/..
 
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2

Analysis of rare Parkinson's disease variants in millions o..:

Pitz, Vanessa ; Makarious, Mary B. ; Bandres-Ciga, Sara...
npj Parkinson's Disease.  10 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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3

Ultra-rare complement factor 8 coding variants in families ..:

Zelinger, Lina ; Martin, Tammy M. ; Advani, Jayshree...
iScience.  26 (2023)  4 - p. 106417 , 2023
Link: https://doi.org/10.1016/..
 
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4

Whole genome sequencing of 4,787 individuals identifies gen..:

Kwong, Alan ; Zawistowski, Matthew ; Fritsche, Lars G...
Human Molecular Genetics.  33 (2023)  4 - p. 374-385 , 2023
Link: https://doi.org/10.1093/..
 
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5

Meta-imputation: An efficient method to combine genotype da..:

Yu, Ketian ; Das, Sayantan ; LeFaive, Jonathon...
The American Journal of Human Genetics.  109 (2022)  6 - p. 1007-1015 , 2022
Link: https://doi.org/10.1016/..
 
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6

Family-based exome sequencing identifies rare coding varian..:

Ratnapriya, Rinki ; Acar, İlhan E ; Geerlings, Maartje J...
Human Molecular Genetics.  29 (2020)  12 - p. 2022-2034 , 2020
Link: https://doi.org/10.1093/..
 
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7

Mutations in MERTK are not associated with age-related macu..:

Al-khersan, Hasenin ; Kwong, Alan ; Grassi, Michael A.
International Ophthalmology.  39 (2018)  1 - p. 63-67 , 2018
Link: https://doi.org/10.1007/..
 
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8

Next-generation genotype imputation service and methods:

Das, Sayantan ; Forer, Lukas ; Schönherr, Sebastian...
Nature Genetics.  48 (2016)  10 - p. 1284-1287 , 2016
Link: https://doi.org/10.1038/..
 
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9

Genome sequencing elucidates Sardinian genetic architecture..:

Sidore, Carlo ; Busonero, Fabio ; Maschio, Andrea...
Nature Genetics.  47 (2015)  11 - p. 1272-1281 , 2015
Link: https://doi.org/10.1038/..
 
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10

In search of rare variants: Preliminary results from whole ..:

Vrieze, Scott I. ; Malone, Stephen M. ; Vaidyanathan, Uma...
Psychophysiology.  51 (2014)  12 - p. 1309-1320 , 2014
Link: https://doi.org/10.1111/..
 
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11

Genetic Variants for Long QT Syndrome among Infants and Chi..:

Chang, Ruey-Kang R. ; Lan, Yueh-Tze ; Silka, Michael J....
The Journal of Pediatrics.  164 (2014)  3 - p. 590-595.e3 , 2014
Link: https://doi.org/10.1016/..
 
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12

Robust, flexible, and scalable tests for Hardy–Weinberg equ..:

Kwong, Alan M ; Blackwell, Thomas W ; LeFaive, Jonathon...
Genetics.  218 (2021)  1 - p. , 2021
Link: https://doi.org/10.1093/..
 
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13

Intestinal tumor suppression in ApcMin/+ mice by prostaglan..:

Tippin, Brigette L. ; Kwong, Alan M. ; Inadomi, Michael J....
Cancer Medicine.  3 (2014)  4 - p. 1041-1051 , 2014
Link: https://doi.org/10.1002/..
 
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14

Hematopoietic prostaglandin D synthase (HPGDS): A high stab..:

Tippin, Brigette L. ; Levine, A. Joan ; Materi, Alicia M....
Prostaglandins & Other Lipid Mediators.  97 (2012)  1-2 - p. 22-28 , 2012
Link: https://doi.org/10.1016/..
 
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15

Asymptomatic Maternal Combined Homocystinuria and Methylmal..:

Lin, Henry J. ; Neidich, Julie A. ; Salazar, Denise...
The Journal of Pediatrics.  155 (2009)  6 - p. 924-927 , 2009
Link: https://doi.org/10.1016/..
 
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