Works matching IS 14345161 AND DT 2010 AND VI 55 AND IP 4

Results: 13

Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 244, doi. 10.1038/jhg.2010.14

By:

Honda, Shozo;
Orii, Koji O.;
Kobayashi, Junya;
Hayashi, Shin;
Imamura, Atsushi;
Imoto, Issei;
Nakagawa, Eiji;
Goto, Yu-ichi;
Inazawa, Johji

Publication type:

Article

Concordance of two multiple analytical approaches demonstrate that interaction between BMI and ADIPOQ haplotypes is a determinant of LDL cholesterol in a general French population.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 227, doi. 10.1038/jhg.2010.10

By:

Vasseur, Francis;
Caeyseele, Thomas;
Barat-Houari, Mouna;
Lobbens, Stéphane;
Meirhaeghe, Aline;
Meyre, David;
Froguel, Philippe;
Amouyel, Philippe;
Helbecque, Nicole

Publication type:

Article

Factor V Leiden mutation in Arabs in Kuwait by real-time PCR: different values for different Arabs.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 232, doi. 10.1038/jhg.2010.11

By:

Dashti, Ali A.;
Jadaon, Mehrez M.;
Lewis, Hend L.

Publication type:

Article

Family-based association study of IGF1 microsatellites and height, weight, and body mass index.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 255, doi. 10.1038/jhg.2010.17

By:

Fehringer, Gordon;
Ozcelik, Hilmi;
Knight, Julia A.;
Paterson, Andrew D.;
Dite, Gillian S.;
Giles, Graham G.;
Southey, Melissa C.;
Andrulis, Irene L.;
Hopper, John L.;
Boyd, Norman F.

Publication type:

Article

Cerebral hemorrhage in Fabry's disease.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 259, doi. 10.1038/jhg.2010.18

By:

Nakamura, Katsuya;
Sekijima, Yoshiki;
Nakamura, Kimitoshi;
Hattori, Kiyoko;
Nagamatsu, Kiyoshiro;
Shimizu, Yusaku;
Yasude, Takuji;
Ushiyama, Masao;
Endo, Fumio;
Fukushima, Yoshimitsu;
Ikeda, Shu-ichi

Publication type:

Article

Resequencing of the CCL5 and CCR5 genes and investigation of variants for association with diabetic nephropathy.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 248, doi. 10.1038/jhg.2010.15

By:

Pettigrew, Kerry A.;
McKnight, Amy Jayne;
Patterson, Christopher C.;
Kilner, Jill;
Sadlier, Denise M.;
Maxwell, Alexander P.

Publication type:

Article

FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 252, doi. 10.1038/jhg.2010.16

By:

Suzuki, Naoki;
Aoki, Masashi;
Warita, Hitoshi;
Kato, Masaaki;
Mizuno, Hideki;
Shimakura, Naoko;
Akiyama, Tetsuya;
Furuya, Hirokazu;
Hokonohara, Toshihiro;
Iwaki, Akiko;
Togashi, Shinji;
Konno, Hidehiko;
Itoyama, Yasuto

Publication type:

Article

A functional epidermal growth factor (EGF) polymorphism, EGF serum levels and renal cell carcinoma risk in a Chinese population.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 236, doi. 10.1038/jhg.2010.12

By:

Jian Zhu;
Xiaoxin Meng;
Fu Yan;
Chao Qin;
Meilin Wang;
Qi Ding;
Pu Li;
Jian Yang;
Xiaobing Ju;
Zhengdong Zhang;
Shui Wang;
Changjun Yin

Publication type:

Article

The heritability of risk and age at onset of Parkinson's disease after accounting for known genetic risk factors.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 241, doi. 10.1038/jhg.2010.13

By:

Hamza, Taye H.;
Payami, Haydeh

Publication type:

Article

The pursuit of genome-wide association studies: where are we now?

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 195, doi. 10.1038/jhg.2010.19

By:

Chee Seng Ku;
En Yun Loy;
Yudi Pawitan;
Kee Seng Chia

Publication type:

Article

Selective neutrality analysis of 17 STRs in Mediterranean populations.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 207, doi. 10.1038/jhg.2010.7

By:

Piras, Ignazio;
Falchi, Alessandra;
Moral, Pedro;
Paoli, Giorgio;
Calò, Carla M.;
Vona, Giuseppe;
Varesi, Laurent

Publication type:

Article

Ancient DNA from nomads in 2500-year-old archeological sites of Pengyang, China.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 215, doi. 10.1038/jhg.2010.8

By:

Yong-Bin Zhao;
Hong-Jie Li;
Da-Wei Cai;
Chun-Xiang Li;
Quan-Chao Zhang;
Hong Zhu;
Hui Zhou

Publication type:

Article

A remark on rare variants.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 4, p. 219, doi. 10.1038/jhg.2010.9

By:

Oexle, Konrad

Publication type:

Article