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Results: 1-25/52
Authors:
Kere, J
Citation: J. Kere, Human population genetics: Lessons from Finland, ANN REV GEN, 2, 2001, pp. 103-128
Authors:
Laitinen, T
Daly, MJ
Rioux, JD
Kauppi, P
Laprise, C
Petays, T
Green, T
Cargill, M
Haahtela, T
Lander, ES
Laitinen, LA
Hudson, TJ
Kere, J
Citation: T. Laitinen et al., A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population, NAT GENET, 28(1), 2001, pp. 87-91
Authors:
Hoglund, P
Sormaala, M
Haila, S
Socha, J
Rajaram, U
Scheurlen, W
Sinaasappel, M
de Jonge, H
Holmberg, C
Yoshikawa, H
Kere, J
Citation: P. Hoglund et al., Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea, HUM MUTAT, 18(3), 2001, pp. 233-242
Authors:
Zhu, Y
Loukola, A
Monni, O
Kuokkanen, K
Franssila, K
Elonen, E
Vilpo, J
Joensuu, H
Kere, J
Aaltonen, L
Knuutila, S
Citation: Y. Zhu et al., PPP2R1B gene in chronic lymphocytic leukemias and mantle cell lymphomas, LEUK LYMPH, 41(1-2), 2001, pp. 177-183
Authors:
Koillinen, H
Wong, FK
Rautio, J
Ollikainen, V
Karsten, A
Larson, O
Teh, BT
Huggare, J
Lahermo, P
Larsson, C
Kere, J
Citation: H. Koillinen et al., Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34, EUR J HUM G, 9(10), 2001, pp. 747-752
Authors:
Barkardottir, RB
Sarantaus, L
Arason, A
Vehmanen, P
Bendahl, PO
Kainu, T
Syrjakoski, K
Krahe, R
Huusko, P
Pyrhonen, S
Holli, K
Kallioniemi, OP
Egilsson, V
Kere, J
Nevanlinna, H
Citation: Rb. Barkardottir et al., Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families, EUR J HUM G, 9(10), 2001, pp. 773-779
Authors:
Elomaa, O
Pulkkinen, K
Hannelius, U
Mikkola, M
Saarialho-Kere, U
Kere, J
Citation: O. Elomaa et al., Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein, HUM MOL GEN, 10(9), 2001, pp. 953-962
Authors:
Asumalahti, K
Laitinen, T
Itkonen-Vatjus, R
Lokki, ML
Suomela, S
Snellman, E
Saarialho-Kere, U
Kere, J
Citation: K. Asumalahti et al., A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele (vol 9, pg 1533, 2000), HUM MOL GEN, 10(3), 2001, pp. 301-301
Authors:
Kauppi, P
Lindblad-Toh, K
Sevon, P
Toivonen, HTT
Rioux, JD
Villapakkam, A
Laitinen, LA
Hudson, TJ
Kere, J
Laitinen, T
Citation: P. Kauppi et al., Second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma, GENOMICS, 77(1-2), 2001, pp. 35-42
Authors:
Hannula, K
Lipsanen-Nyman, M
Scherer, SW
Holmberg, C
Hoglund, P
Kere, J
Citation: K. Hannula et al., Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNA, GENOMICS, 73(1), 2001, pp. 1-9
Authors:
Sevon, P
Ollikainen, V
Onkamo, P
Toivonen, HTT
Mannila, H
Kere, J
Citation: P. Sevon et al., Mining associations between genetic markers, phenotypes, and covariates, GENET EPID, 21, 2001, pp. S588-S593
Authors:
Paakkonen, K
Sauramo, S
Sarantaus, L
Vahteristo, P
Hartikainen, A
Vehmanen, P
Ignatius, J
Ollikainen, V
Kaariainen, H
Vauramo, E
Nevanlinna, H
Krahe, R
Holli, K
Kere, J
Citation: K. Paakkonen et al., Involvement of BRCA1 and BRCA2 in breast cancer in a Western Finnish sub-population, GENET EPID, 20(2), 2001, pp. 239-246
Authors:
Koskenmies, S
Widen, E
Kere, J
Julkunen, H
Citation: S. Koskenmies et al., Familial systemic lupus erythematosus in Finland, J RHEUMATOL, 28(4), 2001, pp. 758-760
Authors:
Kiuru-Kuhlefelt, S
El-Rifai, W
Fanburg-Smith, J
Kere, J
Miettinen, M
Knuutila, S
Citation: S. Kiuru-kuhlefelt et al., Concomitant DNA copy number amplification at 17q and 22q in dermatofibrosarcoma protuberans, CYTOG C GEN, 92(3-4), 2001, pp. 192-195
Authors:
Hannula, K
Kere, J
Pirinen, S
Holmberg, C
Lipsanen-Nyman, M
Citation: K. Hannula et al., Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?, J MED GENET, 38(4), 2001, pp. 273-278
Authors:
Nopola-Hemmi, J
Myllyluoma, B
Haltia, T
Taipale, M
Ollikainen, V
Ahonen, T
Voutilainen, A
Kere, J
Widen, E
Citation: J. Nopola-hemmi et al., A dominant gene for developmental dyslexia on chromosome 3, J MED GENET, 38(10), 2001, pp. 658-664
Authors:
Haila, S
Hastbacka, J
Bohling, T
Karjalainen-Lindsberg, ML
Kere, J
Saarialho-Kere, U
Citation: S. Haila et al., SLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell types, J HIST CYTO, 49(8), 2001, pp. 973-982
Authors:
Hoglund, P
Holmberg, C
Sherman, P
Kere, J
Citation: P. Hoglund et al., Distinct outcomes of chloride diarrhoea in two siblings with identical genetic background of the disease: implications for early diagnosis and treatment, GUT, 48(5), 2001, pp. 724-727
Authors:
Virolainen, E
Niemi, KM
Ganem, A
Kere, J
Vahlquist, A
Saarialho-Kere, U
Citation: E. Virolainen et al., Ultrastructural features resembling those of harlequin ichthyosis in patients with severe congenital ichthyosiform erythroderma, BR J DERM, 145(3), 2001, pp. 480-483
Authors:
Hannula, K
Lipsanen-Nyman, M
Kontiokari, T
Kere, J
Citation: K. Hannula et al., A narrow segment of maternal uniparental disomy of chromosome 7q31-qter inSilver-Russell syndrome delimits a candidate gene region, AM J HU GEN, 68(1), 2001, pp. 247-253
Authors:
Laitinen, T
Ollikainen, V
Lazaro, C
Kauppi, P
de Cid, R
Anto, JM
Estivill, X
Lokki, H
Mannila, H
Laitinen, LA
Kere, J
Citation: T. Laitinen et al., Association study of the chromosomal region containing the FCER2 gene suggests it has a regulatory role in atopic disorders, AM J R CRIT, 161(3), 2000, pp. 700-706
Authors:
Taillon-Miller, P
Bauer-Sardina, I
Saccone, NL
Putzel, J
Laitinen, T
Cao, A
Kere, J
Pilia, G
Rice, JP
Kwok, PY
Citation: P. Taillon-miller et al., Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28, NAT GENET, 25(3), 2000, pp. 324-328
Authors:
Sarantaus, L
Huusko, P
Eerola, H
Launonen, V
Vehmanen, P
Rapakko, K
Gillanders, E
Syrjakoski, K
Kainu, T
Vahteristo, P
Krahe, R
Paakkonen, K
Hartikainen, J
Blomqvist, C
Lopponen, T
Holli, K
Ryynanen, M
Butzow, R
Borg, A
Arver, BW
Holmberg, E
Mannermaa, A
Kere, J
Kallioniemi, OP
Winqvist, R
Nevanlinna, H
Citation: L. Sarantaus et al., Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland, EUR J HUM G, 8(10), 2000, pp. 757-763
Authors:
Kauppi, P
Laitinen, T
Ollikainen, V
Mannila, H
Laitinen, LA
Kere, J
Citation: P. Kauppi et al., The IL9R region contribution in asthma is supported by genetic associationin an isolated population, EUR J HUM G, 8(10), 2000, pp. 788-792
Authors:
Asumalahti, K
Laitinen, T
Itkonen-Vatjus, R
Lokki, ML
Suomela, S
Snellman, E
Saarialho-Kere, U
Kere, J
Citation: K. Asumalahti et al., A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele, HUM MOL GEN, 9(10), 2000, pp. 1533-1542