Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index
(427)
Hoggart, Clive J
a
Venturini, Giulia
b
Mangino, Massimo
c,m
Gomez, Felicia
d
Ascari, Giulia
b
Zhao, Jing Hua
e,m
Teumer, Alexander
f,m
Winkler, Thomas W
g,m
Tšernikova, Natalia
h,i
Luan, Jian'an
e,m
Mihailov, Evelin
h,m
Ehret, Georg B
j,k
Zhang, Weihua
a
Lamparter, David
b,l
Esko, Tõnu
m,n,o
Macé, Aurelien
b,l
Rüeger, Sina
b,l
Bochud, Pierre Yves
p
Barcella, Matteo
q
Dauvilliers, Yves
r,s
Benyamin, Beben
t,u
Evans, David M
m,t,v,w
Hayward, Caroline
m,x
Lopez, Mary F
m,n,o
Franke, Lude
m,y
Russo, Alessia
z
Heid, Iris M
g,m
Salvi, Erika
q
Vendantam, Sailaja
m,n
Arking, Dan E
j
Boerwinkle, Eric
m,aa
Chambers, John C
a
Fiorito, Giovanni
z
Grallert, Harald
m,ab
Guarrera, Simonetta
ac
Homuth, Georg
f,m
Huffman, Jennifer E
m,x
Porteous, David
x
Moradpour, Darius
ad
Iranzo, Alex
ae
Hebebrand, Johannes
m,af
Kemp, John P
v,w
Lammers, Gert J
ag,ah
Aubert, Vincent
p
Heim, Markus H
ai
Martin, Nicholas G
m,u
Montgomery, Grant W
m,u
Peraita Adrados, Rosa
aj
Santamaria, Joan
ae
Negro, Francesco
ak
Schmidt, Carsten O
f
Scott, Robert A
e
Spector, Timothy D
m
Strauch, Konstantin
ab,al
Völzke, Henry
f
Wareham, Nicholas J
e,m
Yuan, Wei
c
Bell, Jordana T
c
Chakravarti, Aravinda
j
Kooner, Jaspal S
am
Peters, Annette
m,ab,an
Matullo, Giuseppe
z
Wallaschofski, Henri
f,m
Whitfield, John B
u
Paccaud, Fred
ao
Vollenweider, Peter
m,p
Bergmann, Sven
b,l
Beckmann, Jacques S
l
Tafti, Mehdi
b,p
Hastie, Nicholas D
x
Cusi, Daniele
m,q
Bochud, Murielle
ao
Frayling, Timothy M
ap
Metspalu, Andres
h,i,m
Jarvelin, Marjo Riitta
aq,ar,as,at
Scherag, André
m,au,av
Smith, George Davey
v,w
Borecki, Ingrid B
d,m
Rousson, Valentin
ao
Hirschhorn, Joel N
m,n,o
Rivolta, Carlo
b
Loos, Ruth J F
e,m,aw
Kutalik, Zoltán
b,l,m,ao
de Bakker, P
y
Bultmann U
y
Geleijnse, M
y
van der Harst, P
y
Koppelman, G
y
Rosmalen, J G M
y
van Rossum, L
y
Smidt, H
y
Swertz, M A
y
Stolk, R P
y
Alizadeh, B
y
de Boer, R
y
Boezen, H M
y
Bruinenberg, M
y
Hillege, H
y
van der Klauw, M
y
Navis, G
y
Ormel, J
y
Postma, D
y
Slaets, J
y
Snieder, H
y
Wolffenbuttel, B
y
Wijmenga, C
y
Berg, Jonathan
x
Blackwood, Douglas
x
Campbell, Harry
m,x
Cavanagh, Jonathan
x
Connell, John
x
Connor, Mike
x
Cunningham Burley, Sarah
x
Deary, Ian
x
Dominiczak, Anna
x
Ellis, Paul
x
FitzPatrick, Bridie
x
Ford, Ian
x
Gertz, Rena
x
Grau, Antonio
x
Haddow, Gill
x
Jackson, Cathy
x
Kerr, Shona
x
Lindsay, Robbie
x
McGilchrist, Mark
x
McIntyre, Donald
x
Morris, Andrew
x
Morton, Robin
x
Muir, Walter
x
Murray, Graeme
x
Randy, P
x
Pell, Jill
x
Philp, Alastair
x
Porteous, Mary
x
Procter, Rob
x
Ralston, Stuart
x
Reid, David
x
Sinnott, Richard
x
Smith, Blair
x
St Clair, David
x
Sullivan, Frank
x
Sweetland, Mary
x
Ure, Jenny
x
Watt, Graham
x
Wolf, Roland
x
Wright, Alan
x
Berndt, Sonja I
m
Gustafsson, Stefan
m
Mägi, Reedik
m
Ganna, Andrea
m
Wheeler, Eleanor
m
Feitosa, Mary F
m
Justice, Anne E
m
Monda, Keri L
m
Croteau Chonka, Damien C
m
Day, Felix R
m
Fall, Tove
m
Ferreira, Teresa
m
Gentilini, Davide
m
Jackson, Anne U
m
Randall, Joshua C
m
Vedantam, Sailaja
m
Willer, Cristen J
m
Wood, Andrew R
m
Workalemahu, Tsegaselassie
m
Hu, Yi Juan
m
Hong Lee, Sang
m
Liang, Liming
m
Lin, Dan Yu
m
Min, Josine L
m
Neale, Benjamin M
m
Thorleifsson, Gudmar
m
Yang, Jian
m
Albrecht, Eva
m
Amin, Najaf
m
Bragg Gresham, Jennifer L
m
Cadby, Gemma
m
den Heijer, Martin
m
Eklund, Niina
m
Fischer, Krista
m
Goel, Anuj
m
Hottenga, Jouke Jan
m
Jarick, Ivonne
m
Johansson, Asa
m
Johnson, Toby
m
Kanoni, Stavroula
m
Kleber, Marcus E
m
König, Inke R
m
Kristiansson, Kati
m
Lamina, Claudia
m
Lecoeur, Cecile
m
Li, Guo
m
McArdle, Wendy L
m
Medina Gomez, Carolina
m
Müller Nurasyid, Martina
m
Ngwa, Julius S
m
Nolte, Ilja M
m
Paternoster, Lavinia
m
Pechlivanis, Sonali
m
Perola, Markus
m
Peters, Marjolein J
m
Preuss, Michael
m
Rose, Lynda M
m
Shi, Jianxin
m
Shungin, Dmitry
m
Smith, Albert Vernon
m
Strawbridge, Rona J
m
Surakka, Ida
m
Trip, Mieke D
m
Tyrer, Jonathan
m
Van Vliet Ostaptchouk, Jana V
m
Vandenput, Liesbeth
m
Waite, Lindsay L
m
Absher, Devin
m
Asselbergs, Folkert W
m
Atalay, Mustafa
m
Attwood, Antony P
m
Balmforth, Anthony J
m
Basart, Hanneke
m
Beilby, John
m
Bonnycastle, Lori L
m
Brambilla, Paolo
m
Chasman, Daniel I
m
Chines, Peter S
m
Collins, Francis S
m
Cookson, William
m
de Faire, Ulf
m
de Vegt, Femmie
m
Dei, Mariano
m
Dimitriou, Maria
m
Edkins, Sarah
m
Estrada, Karol
m
Farrall, Martin
m
Ferrario, Marco M
m
Ferrières, Jean
m
Frau, Francesca
m
Gejman, Pablo V
m
Grönberg, Henrik
m
Gudnason, Vilmundur
m
Hall, Alistair S
m
Hall, Per
m
Hartikainen, Anna Liisa
m
Heard Costa, Nancy L
m
Heath, Andrew C
m
Hu, Frank B
m
Hunt, Sarah E
m
Hyppönen, Elina
m
Iribarren, Carlos
m
Jacobs, Kevin B
m
Jansson, John Olov
m
Jula, Antti
m
Kähönen, Mika
m
Kathiresan, Sekar
m
Kee, Frank
m
Khaw, Kay Tee
m
Kivimaki, Mika
m
Koenig, Wolfgang
m
Kraja, Aldi T
m
Kumari, Meena
m
Kuulasmaa, Kari
m
Kuusisto, Johanna
m
Laitinen, Jaana H
m
Lakka, Timo A
m
Langenberg, Claudia
m
Launer, Lenore J
m
Lind, Lars
m
Lindström, Jaana
m
Liu, Jianjun
m
Liuzzi, Antonio
m
Lokki, Marja Liisa
m
Lorentzon, Mattias
m
Madden, Pamela A
m
Magnusson, Patrik K
m
Manunta, Paolo
m
Marek, Diana
m
Mä rz, Winfried
m
Leach, Irene Mateo
m
McKnight, Barbara
m
Medland, Sarah E
m
Milani, Lili
m
Mooser, Vincent
m
Mühleisen, Thomas W
m
Munroe, Patricia B
m
Musk, Arthur W
m
Narisu, Narisu
m
Nicholson, George
m
Nohr, Ellen A
m
Ong, Ken K
m
Oostra, Ben A
m
Palmer, Colin N A
m
Palotie, Aarno
m
Peden, John F
m
Pedersen, Nancy
m
Polasek, Ozren
m
Pouta, Anneli
m
Pramstaller, Peter P
m
Prokopenko, Inga
m
Pü tter, Carolin
m
Radhakrishnan, Aparna
m
Raitakari, Olli
m
Rendon, Augusto
m
Rivadeneira, Fernando
m
Rudan, Igor
m
Saaristo, Timo E
m
Sambrook, Jennifer G
m
Sanders, Alan R
m
Sanna, Serena
m
Saramies, Jouko
m
Schipf, Sabine
m
Schreiber, Stefan
m
Schunkert, Heribert
m
Shin, So Youn
m
Signorini, Stefano
m
Sinisalo, Juha
m
Skrobek, Boris
m
Soranzo, Nicole
m
Stancakova, Alena
m
Stark, Klaus
m
Stephens, Jonathan C
m
Stirrups, Kathleen
m
Stumvoll, Michael
m
Swift, Amy J
m
Theodoraki, Eirini V
m
Thorand, Barbara
m
Tregouet, David Alexandre
m
Tremoli, Elena
m
van Meurs, Joyce B J
m
Vermeulen, Sita H
m
Viikari, Jorma
m
Virtamo, Jarmo
m
Vitart, Veronique
m
Waeber, Gérard
m
Wang, Zhaoming
m
Widen, Elisabeth
m
Wild, Sarah H
m
Willemsen, Gonneke
m
Winkelmann, Bernhard R
m
Witteman, Jacqueline C M
m
Wong, Andrew
m
Wright, Alan F
m
Zillikens, M Carola
m
Amouyel, Philippe
m
Boehm, Bernhard O
m
Boomsma, Dorret I
m
Caulfield, Mark J
m
Chanock, Stephen J
m
Cupples, L Adrienne
m
Dedoussis, George V
m
Erdmann, Jeanette
m
Eriksson, Johan G
m
Franks, Paul W
m
Froguel, Philippe
m
Gieger, Christian
m
Gyllensten, Ulf
m
Hamsten, Anders
m
Harris, Tamara B
m
Hengstenberg, Christian
m
Hicks, Andrew A
m
Hingorani, Aroon
m
Hinney, Anke
m
Hofman, Albert
m
Hovingh, Kees G
m
Hveem, Kristian
m
Illig, Thomas
m
Ingelsson, Erik
m
Jöckel, Karl Heinz
m
Keinanen Kiukaanniemi, Sirkka M
m
Kiemeney, Lambertus A
m
Kuh, Diana
m
Laakso, Markku
m
Lehtimäki, Terho
m
Levinson, Douglas F
m
Morris, Andrew D
m
Nieminen, Markku S
m
Njølstad, Inger
m
Ohlsson, Claes
m
Oldehinkel, Albertine J
m
Ouwehand, Willem H
m
Palmer, Lyle J
m
Penninx, Brenda
m
Power, Chris
m
Province, Michael A
m
Psaty, Bruce M
m
Qi, Lu
m
Rauramaa, Rainer
m
Ridker, Paul M
m
Ripatti, Samuli
m
Salomaa, Veikko
m
Samani, Nilesh J
m
Sørensen, Thorkild I A
m
Stefansson, Kari
m
Tönjes, Anke
m
Tuomilehto, Jaakko
m
Uitterlinden, André G
m
Uusitupa, Matti
m
Watkins, Hugh
m
Wichmann, H Erich
m
Wilson, James F
m
Abecasis, Goncalo R
m
Assimes, Themistocles L
m
Barroso, Ines
m
Boehnke, Michael
m
Deloukas, Panos
m
Fox, Caroline S
m
Groop, Leif C
m
Haritunian, Talin
m
Hunter, David
m
Kaplan, Robert C
m
Karpe, Fredrik
m
Moffatt, Miriam
m
Mohlke, Karen L
m
O'Connell, Jeffrey R
m
Pawitan, Yudi
m
Schadt, Eric E
m
Schlessinger, David
m
Steinthorsdottir, Valgerdur
m
Strachan, David P
m
Thorsteinsdottir, Unnur
m
van Duijn, Cornelia M
m
Visscher, Peter M
m
Di Blasio, Anna Maria
m
Lindgren, Cecilia M
m
Morris, Andrew P
m
Meyre, David
m
McCarthy, Mark I
m
Speliotes, Elizabeth K
m
North, Kari E
m
more..
|
-
1
-
-
72449122779
-
Parental origin of sequence variants associated with complex diseases
-
Kong A, Steinthorsdottir V, Masson G, Thorleifsson G, Sulem P, et al. (2009) Parental origin of sequence variants associated with complex diseases. Nature 462: 868-874.
-
(2009)
Nature
, vol.462
, pp. 868-874
-
-
Kong, A.1
Steinthorsdottir, V.2
Masson, G.3
Thorleifsson, G.4
Sulem, P.5
-
2
-
-
59849089649
-
Investigating parent of origin effects in studies of type 2 diabetes and obesity
-
Rampersaud E, Mitchell BD, Naj AC, Pollin TI (2008) Investigating parent of origin effects in studies of type 2 diabetes and obesity. Curr Diabetes Rev 4: 329-339.
-
(2008)
Curr Diabetes Rev
, vol.4
, pp. 329-339
-
-
Rampersaud, E.1
Mitchell, B.D.2
Naj, A.C.3
Pollin, T.I.4
-
3
-
-
84882448216
-
Genomic imprinting and parent-oforigin effects on complex traits
-
Lawson HA, Cheverud JM, Wolf JB (2013) Genomic imprinting and parent-oforigin effects on complex traits. Nat Rev Genet 14: 609-617.
-
(2013)
Nat Rev Genet
, vol.14
, pp. 609-617
-
-
Lawson, H.A.1
Cheverud, J.M.2
Wolf, J.B.3
-
4
-
-
84856489941
-
Parent of origin effects
-
Guilmatre A, Sharp AJ (2012) Parent of origin effects. Clin Genet 81: 201-209.
-
(2012)
Clin Genet
, vol.81
, pp. 201-209
-
-
Guilmatre, A.1
Sharp, A.J.2
-
5
-
-
13844253255
-
Possible genomic imprinting of three human obesity-related genetic loci
-
Dong C, Li WD, Geller F, Lei L, Li D, et al. (2005) Possible genomic imprinting of three human obesity-related genetic loci. Am J Hum Genet 76: 427-437.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 427-437
-
-
Dong, C.1
Li, W.D.2
Geller, F.3
Lei, L.4
Li, D.5
-
6
-
-
0035653510
-
Genomewide linkage analysis assessing parent-of-origin effects in the inheritance of type 2 diabetes and BMI in Pima Indians
-
Lindsay RS, Kobes S, Knowler WC, Bennett PH, Hanson RL (2001) Genomewide linkage analysis assessing parent-of-origin effects in the inheritance of type 2 diabetes and BMI in Pima Indians. Diabetes 50: 2850-2857.
-
(2001)
Diabetes
, vol.50
, pp. 2850-2857
-
-
Lindsay, R.S.1
Kobes, S.2
Knowler, W.C.3
Bennett, P.H.4
Hanson, R.L.5
-
9
-
-
30344443527
-
Linkage analysis of alcohol dependence using MOD scores
-
Strauch K, Furst R, Ruschendorf F, Windemuth C, Dietter J, et al. (2005) Linkage analysis of alcohol dependence using MOD scores. BMC Genet 6 Suppl 1: S162.
-
(2005)
BMC Genet 6 Suppl
, vol.1
-
-
Strauch, K.1
Furst, R.2
Ruschendorf, F.3
Windemuth, C.4
Dietter, J.5
-
10
-
-
78049337953
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
-
Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, et al. (2010) Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet 42: 937-948.
-
(2010)
Nat Genet
, vol.42
, pp. 937-948
-
-
Speliotes, E.K.1
Willer, C.J.2
Berndt, S.I.3
Monda, K.L.4
Thorleifsson, G.5
-
11
-
-
48449105481
-
Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9
-
Barel O, Shalev SA, Ofir R, Cohen A, Zlotogora J, et al. (2008) Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9. Am J Hum Genet 83: 193-199.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 193-199
-
-
Barel, O.1
Shalev, S.A.2
Ofir, R.3
Cohen, A.4
Zlotogora, J.5
-
12
-
-
80052864661
-
Novel locus FER is associated with serum HMW adiponectin levels
-
Qi L, Menzaghi C, Salvemini L, De Bonis C, Trischitta V, et al. (2011) Novel locus FER is associated with serum HMW adiponectin levels. Diabetes 60: 2197-2201.
-
(2011)
Diabetes
, vol.60
, pp. 2197-2201
-
-
Qi, L.1
Menzaghi, C.2
Salvemini, L.3
De Bonis, C.4
Trischitta, V.5
-
13
-
-
84868616005
-
Variations in the potassium channel genes KCNK3 and KCNK9 in relation to blood pressure and aldosterone production: An exploratory study
-
Jung J, Barrett PQ, Eckert GJ, Edenberg HJ, Xuei X, et al. (2012) Variations in the potassium channel genes KCNK3 and KCNK9 in relation to blood pressure and aldosterone production: an exploratory study. J Clin Endocrinol Metab 97: E2160-2167.
-
(2012)
J Clin Endocrinol Metab
, vol.97
, pp. E2160-E2167
-
-
Jung, J.1
Barrett, P.Q.2
Eckert, G.J.3
Edenberg, H.J.4
Xuei, X.5
-
14
-
-
70350443586
-
An unexpected role for TASK-3 potassium channels in network oscillations with implications for sleep mechanisms and anesthetic action
-
Pang DS, Robledo CJ, Carr DR, Gent TC, Vyssotski AL, et al. (2009) An unexpected role for TASK-3 potassium channels in network oscillations with implications for sleep mechanisms and anesthetic action. Proc Natl Acad Sci U S A 106: 17546-17551.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 17546-17551
-
-
Pang, D.S.1
Robledo, C.J.2
Carr, D.R.3
Gent, T.C.4
Vyssotski, A.L.5
-
15
-
-
36348934072
-
TASK-3 knockout mice exhibit exaggerated nocturnal activity, impairments in cognitive functions, and reduced sensitivity to inhalation anesthetics
-
Linden AM, Sandu C, Aller MI, Vekovischeva OY, Rosenberg PH, et al. (2007) TASK-3 knockout mice exhibit exaggerated nocturnal activity, impairments in cognitive functions, and reduced sensitivity to inhalation anesthetics. J Pharmacol Exp Ther 323: 924-934.
-
(2007)
J Pharmacol Exp Ther
, vol.323
, pp. 924-934
-
-
Linden, A.M.1
Sandu, C.2
Aller, M.I.3
Vekovischeva, O.Y.4
Rosenberg, P.H.5
-
16
-
-
59949103364
-
Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
-
Lowe JK, Maller JB, Pe'er I, Neale BM, Salit J, et al. (2009) Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. PLoS Genet 5: e1000365.
-
(2009)
PLoS Genet
, vol.5
-
-
Lowe, J.K.1
Maller, J.B.2
Pe'er, I.3
Neale, B.M.4
Salit, J.5
-
17
-
-
78751700313
-
Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis
-
Jarick I, Vogel CI, Scherag S, Schafer H, Hebebrand J, et al. (2011) Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis. Hum Mol Genet 20: 840-852.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 840-852
-
-
Jarick, I.1
Vogel, C.I.2
Scherag, S.3
Schafer, H.4
Hebebrand, J.5
-
18
-
-
79952758953
-
Genome-wide assessment of imprinted expression in human cells
-
Morcos L, Ge B, Koka V, Lam KC, Pokholok DK, et al. (2011) Genome-wide assessment of imprinted expression in human cells. Genome Biol 12: R25.
-
(2011)
Genome Biol
, vol.12
-
-
Morcos, L.1
Ge, B.2
Koka, V.3
Lam, K.C.4
Pokholok, D.K.5
-
19
-
-
37749009110
-
A genomewide approach to identifying novel-imprinted genes
-
Pollard KS, Serre D, Wang X, Tao H, Grundberg E, et al. (2008) A genomewide approach to identifying novel-imprinted genes. Hum Genet 122: 625-634.
-
(2008)
Hum Genet
, vol.122
, pp. 625-634
-
-
Pollard, K.S.1
Serre, D.2
Wang, X.3
Tao, H.4
Grundberg, E.5
-
20
-
-
50149083052
-
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: First evidence of polar overdominance in humans
-
Wermter AK, Scherag A, Meyre D, Reichwald K, Durand E, et al. (2008) Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans. Eur J Hum Genet 16: 1126-1134.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 1126-1134
-
-
Wermter, A.K.1
Scherag, A.2
Meyre, D.3
Reichwald, K.4
Durand, E.5
-
21
-
-
78049349396
-
Metaanalysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
-
Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, et al. (2010) Metaanalysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet 42: 949-960.
-
(2010)
Nat Genet
, vol.42
, pp. 949-960
-
-
Heid, I.M.1
Jackson, A.U.2
Randall, J.C.3
Winkler, T.W.4
Qi, L.5
-
22
-
-
33645080977
-
Model for mapping imprinted quantitative trait loci in an inbred F2 design
-
Cui Y, Lu Q, Cheverud JM, Littell RC, Wu R (2006) Model for mapping imprinted quantitative trait loci in an inbred F2 design. Genomics 87: 543-551.
-
(2006)
Genomics
, vol.87
, pp. 543-551
-
-
Cui, Y.1
Lu, Q.2
Cheverud, J.M.3
Littell, R.C.4
Wu, R.5
-
23
-
-
85162688577
-
-
Yang J, Loos RJ, Powell JE, Medland SE, Speliotes EK, et al. (2012) FTO genotype is associated with phenotypic variability of body mass index. Nature.
-
Yang J, Loos RJ, Powell JE, Medland SE, Speliotes EK, et al. (2012) FTO genotype is associated with phenotypic variability of body mass index. Nature
-
-
-
-
24
-
-
84881662190
-
What Is the Significance of Difference in Phenotypic Variability across SNP Genotypes?
-
Sun X, Elston R, Morris N, Zhu X (2013) What Is the Significance of Difference in Phenotypic Variability across SNP Genotypes? Am J Hum Genet 93: 390-397.
-
(2013)
Am J Hum Genet
, vol.93
, pp. 390-397
-
-
Sun, X.1
Elston, R.2
Morris, N.3
Zhu, X.4
-
25
-
-
84866171022
-
Inheritance beyond plain heritability: Variance-controlling genes in Arabidopsis thaliana
-
Shen X, Pettersson M, Ronnegard L, Carlborg O (2012) Inheritance beyond plain heritability: variance-controlling genes in Arabidopsis thaliana. PLoS Genet 8: e1002839.
-
(2012)
PLoS Genet
, vol.8
-
-
Shen, X.1
Pettersson, M.2
Ronnegard, L.3
Carlborg, O.4
-
26
-
-
61849173808
-
Haplotype associations with quantitative traits in the presence of complex multilocus and heterogeneous effects
-
Shibata K, Diatchenko L, Zaykin DV (2009) Haplotype associations with quantitative traits in the presence of complex multilocus and heterogeneous effects. Genet Epidemiol 33: 63-78.
-
(2009)
Genet Epidemiol
, vol.33
, pp. 63-78
-
-
Shibata, K.1
Diatchenko, L.2
Zaykin, D.V.3
-
27
-
-
33749567351
-
Assessment of genetic linkage and parent-of-origin effects on obesity
-
Guo YF, Shen H, Liu YJ, Wang W, Xiong DH, et al. (2006) Assessment of genetic linkage and parent-of-origin effects on obesity. J Clin Endocrinol Metab 91: 4001-4005.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 4001-4005
-
-
Guo, Y.F.1
Shen, H.2
Liu, Y.J.3
Wang, W.4
Xiong, D.H.5
-
28
-
-
35148861667
-
Is there an intrauterine influence on obesity? Evidence from parent child associations in the Avon Longitudinal Study of Parents and Children (ALSPAC)
-
Davey Smith G, Steer C, Leary S, Ness A (2007) Is there an intrauterine influence on obesity? Evidence from parent child associations in the Avon Longitudinal Study of Parents and Children (ALSPAC). Arch Dis Child 92: 876-880.
-
(2007)
Arch Dis Child
, vol.92
, pp. 876-880
-
-
Davey Smith, G.1
Steer, C.2
Leary, S.3
Ness, A.4
-
29
-
-
84880404584
-
Maternal and paternal body mass index and offspring obesity: A systematic review
-
Patro B, Liber A, Zalewski B, Poston L, Szajewska H, et al. (2013) Maternal and paternal body mass index and offspring obesity: a systematic review. Ann Nutr Metab 63: 32-41.
-
(2013)
Ann Nutr Metab
, vol.63
, pp. 32-41
-
-
Patro, B.1
Liber, A.2
Zalewski, B.3
Poston, L.4
Szajewska, H.5
-
30
-
-
84885212429
-
Stronger influence of maternal than paternal obesity on infant and early childhood body mass index: The Fels Longitudinal Study
-
Linabery AM, Nahhas RW, Johnson W, Choh AC, Towne B, et al. (2013) Stronger influence of maternal than paternal obesity on infant and early childhood body mass index: the Fels Longitudinal Study. Pediatr Obes 8: 159-169.
-
(2013)
Pediatr Obes
, vol.8
, pp. 159-169
-
-
Linabery, A.M.1
Nahhas, R.W.2
Johnson, W.3
Choh, A.C.4
Towne, B.5
-
31
-
-
77955140508
-
The Impact of Levene's Test of Equality of Variances on Statistical Theory and Practice
-
Gastwirth JL, Gel YL, Miao W (2009) The Impact of Levene's Test of Equality of Variances on Statistical Theory and Practice. Statistical Science 24: 343-360.
-
(2009)
Statistical Science
, vol.24
, pp. 343-360
-
-
Gastwirth, J.L.1
Gel, Y.L.2
Miao, W.3
-
32
-
-
0342702370
-
Testing Variances in Psychological and Educational-Research
-
Ramsey PH (1994) Testing Variances in Psychological and Educational-Research. J Educ Stat 19: 23-42.
-
(1994)
J Educ Stat
, vol.19
, pp. 23-42
-
-
Ramsey, P.H.1
-
33
-
-
43249090541
-
A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms
-
Gao X, Starmer J, Martin ER (2008) A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms. Genet Epidemiol 32: 361-369.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 361-369
-
-
Gao, X.1
Starmer, J.2
Martin, E.R.3
-
34
-
-
79960527502
-
Detection of parent-oforigin effects for quantitative traits in complete and incomplete nuclear families with multiple children
-
He F, Zhou JY, Hu YQ, Sun F, Yang J, et al. (2011) Detection of parent-oforigin effects for quantitative traits in complete and incomplete nuclear families with multiple children. Am J Epidemiol 174: 226-233.
-
(2011)
Am J Epidemiol
, vol.174
, pp. 226-233
-
-
He, F.1
Zhou, J.Y.2
Hu, Y.Q.3
Sun, F.4
Yang, J.5
-
35
-
-
34147119077
-
Overcoming the winner's curse: Estimating penetrance parameters from case-control data
-
Zollner S, Pritchard JK (2007) Overcoming the winner's curse: estimating penetrance parameters from case-control data. Am J Hum Genet 80: 605-615.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 605-615
-
-
Zollner, S.1
Pritchard, J.K.2
-
36
-
-
52949149311
-
From linkage maps to quantitative trait loci: The history and science of the Utah genetic reference project
-
Prescott SM, Lalouel JM, Leppert M (2008) From linkage maps to quantitative trait loci: the history and science of the Utah genetic reference project. Annu Rev Genomics Hum Genet 9: 347-358.
-
(2008)
Annu Rev Genomics Hum Genet
, vol.9
, pp. 347-358
-
-
Prescott, S.M.1
Lalouel, J.M.2
Leppert, M.3
-
37
-
-
53349117799
-
Two transacting eQTLs modulate the penetrance of PRPF31 mutations
-
Rio Frio T, Civic N, Ransijn A, Beckmann JS, Rivolta C (2008) Two transacting eQTLs modulate the penetrance of PRPF31 mutations. Hum Mol Genet 17: 3154-3165.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3154-3165
-
-
Rio Frio, T.1
Civic, N.2
Ransijn, A.3
Beckmann, J.S.4
Rivolta, C.5
|