Results : 51-75/85
Authors:
Weber, James L.
David, Donna
Heil, Jeremy
Fan, Ying
Zhao, Chengfeng
Marth, Gabor
Journal: American journal of human genetics
Citation: L. Weber, James et al., Human Diallelic Insertion/Deletion Polymorphisms, American journal of human genetics , 71(4), 2002, pp. 854-862
Authors:
Visapää, Ilona
Fellman, Vineta
Vesa, Jouni
Dasvarma, Ayan
Hutton, Jenna L.
Kumar, Vijay
Payne, Gregory S.
Makarow, Marja
Van Coster, Rudy
Taylor, Robert W.
Turnbull, Douglass
Suomalainen, Anu
Peltonen, Leena
Journal: American journal of human genetics
Citation: Visapää, Ilona et al., GRACILE Syndrome, a Lethal Metabolic Disorder with Iron Overload, Is Caused by a Point Mutation in BCS1L, American journal of human genetics , 71(4), 2002, pp. 863-876
Authors:
Stefansson, Hreinn
Petursson, Hannes
Sigurdsson, Engilbert
Steinthorsdottir, Valgerdur
Bjornsdottir, SOley
Sigmundsson, Thordur
Ghosh, Shyamali
Brynjolfsson, Jon
Gunnarsdottir, Steinunn
Ivarsson, Omar
Chou, Thomas T.
Hjaltason, Omar
Birgisdottir, Birgitta
Jonsson, Helgi
Gudnadottir, Vala G.
Gudmundsdottir, Elsa
Bjornsson, Asgeir
Ingvarsson, Brynjolfur
Ingason, Andres
Sigfusson, Sigmundur
Hardardottir, Hronn
Harvey, Richard P.
Lai, Donna
Zhou, Mingdong
Brunner, Daniela
Mutel, Vincent
Gonzalo, Acuna
Lemke, Greg
Sainz, Jesus
Johannesson, Gardar
Andresson, Thorkell
Gudbjartsson, Daniel
Manolescu, Andrei
Frigge, Michael L.
Gurney, Mark E.
Kong, Augustiine
Gulcher, Jeffrey R.
Stefansson, Kari
Journal: American journal of human genetics
Citation: Stefansson, Hreinn et al., Neuregulin 1 and Susceptibility to Schizophrenia, American journal of human genetics , 71(4), 2002, pp. 877-892
Authors:
Angius, Andrea
Petretto, Enrico
Maestrale, Giovanni Battista
Forabosco, Paolo
Casu, Giuseppina
Piras, Daniela
Fanciulli, Manuela
Falchi, Mario
Melis, Paola Maria
Palermo, Mario
Pirastu, Mario
Journal: American journal of human genetics
Citation: Angius, Andrea et al., A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search, American journal of human genetics , 71(4), 2002, pp. 893-905
Authors:
Repping, Sjoerd
Skaletsky, Helen
Lange, Julian
Silber, Sherman
Veen, Fulco, Van : der
Oates, Robert D.
Page, David C.
Rozen, Steve
Journal: American journal of human genetics
Citation: Repping, Sjoerd et al., Recombination between Palindromes P5 and P1 on the Human Y Chromosome Causes Massive Deletions and Spermatogenic Failure, American journal of human genetics , 71(4), 2002, pp. 906-922
Authors:
Coffee, Bradford
Zhang, Fuping
Ceman, Stephanie
Warren, Stephen T.
Reines, Daniel
Journal: American journal of human genetics
Citation: Coffee, Bradford et al., Histone Modifications Depict an Aberrantly Heterochromatinized FMR1 Gene in Fragile X Syndrome, American journal of human genetics , 71(4), 2002, pp. 923-932
Authors:
Pendleton, Andrian
Johnson, Michelle D.
Hughes, Anne
Gurley, Kyle A.
Ho, Andrew M.
Doherty, Michael
Dixey, Josh
Gillet, Pierre
Loeuille, Damien
McGrath, Rodney
Reginato, Antonio
Shiang, Rita
Wright, Gary
Netter, Patrick
Williams, Charlene
Kingsley, David M.
Journal: American journal of human genetics
Citation: Pendleton, Andrian et al., Mutations in ANKH Cause Chondrocalcinosis, American journal of human genetics , 71(4), 2002, pp. 933-94
Authors:
Hallmayer, Joachim
Glasson, Emma J.
Bower, Carol
Petterson, Beverly
Croen, Lisa
Grether, Judith
Risch, Neil
Journal: American journal of human genetics
Citation: Hallmayer, Joachim et al., On the Twin Risk in Autism, American journal of human genetics , 71(4), 2002, pp. 941-946
Authors:
Crosby, Andrew H.
Proukakis, Christos
Journal: American journal of human genetics
Citation: H. Crosby, Andrew et Proukakis, Christos, Is the Transportation Highway the Right Road for Hereditary Spastic Paraplegia?, American journal of human genetics , 71(5), 2002, pp. 1009-1016
Authors:
Ming, Jeffrey E.
Muenke, Maximilian
Journal: American journal of human genetics
Citation: E. Ming, Jeffrey et Muenke, Maximilian, Multiple Hits during Early Embryonic Development: Digenic Diseases and Holoprosencephaly, American journal of human genetics , 71(5), 2002, pp. 1017-1032
Authors:
Beltrán-Valero de Bernabé, Daniel
Currier, Sophie
Steinbrecher, Alice
Celli, Jacopo
Beusekom, Ellen, Van
Zwaag, Bert, Van: der
Kayserili, Hülya
Merlini, Luciano
Chitayat, David
Dobyns, William B.
Cormand, Bru
Lehesjoki, Ana-Elina
Cruces, Jesùs
Voit, Thomas
Walsh, Christopher A.
Bokhoven, Hans, Van
Brunner, Han G.
Journal: American journal of human genetics
Citation: Beltrán-valero De Bernabé, Daniel et al., Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome, American journal of human genetics , 71(5), 2002, pp. 1033-1043
Authors:
Atwoosd, Larry D.
Heard-Costa, Nancy L.
Cupples, L. Adrienne
Jaquish, Cashell E.
Wilson, Peter W.F.
D'Agostino, Ralph B.
Journal: American journal of human genetics
Citation: D. Atwoosd, Larry et al., Genomewide Linkage Analysis of Body Mass Index across 28 Years of the Framingham Heart Study, American journal of human genetics , 71(5), 2002, pp. 1044-1050
Authors:
Lemkel. Johannes
Claussen, Jan
Michel, Susanne
Chudoba, Ilse
Mühlig, Peter
Westermann, Martin
Sperling, Karl
Rubtsov, Nikolai
Grummt, Ulrich-Walter
Ullmann, Peter
Kromeyer-Hauschild, Katrin
Liehr, Thomas
Claussen, Uwe
Journal: American journal of human genetics
Citation: Lemkel. Johannes et al., The DNA-Based Structure of Human Chromosome 5 in Interphase, American journal of human genetics , 71(5), 2002, pp. 1051-1059
Authors:
Johanneson, Bo
Lima, Guadalupe
von Salomé, Jenny
Alarcón-Segovia, Donato
The Collaborative Group on the Genetics of SLE
The BIOMED II Collaboration on the Genetics of SLE and Sjögrens Syndrome
Alarcón-Riquelme, Marta E.
Journal: American journal of human genetics
Citation: Johanneson, Bo et al., A Major Susceptibility Locus for Systemic Lupus Erythemathosus Maps to Chromosome 1q31, American journal of human genetics , 71(5), 2002, pp. 1060-1071
Authors:
Shaw, Christine J.
Bi, Weimin
Lupski, James R.
Journal: American journal of human genetics
Citation: J. Shaw, Christine et al., Genetic Proof of Unequal Meiotic Crossovers in Reciprocal Deletion and Duplication of 17p11.2, American journal of human genetics , 71(5), 2002, pp. 1072-1081
Authors:
Salas, Antono
Richards, Martin
De la Fe, Tomàs
Lareau, Marìa-Victoria
Sobrino, Beatriz
Sànchez-Diz, Paula
Macaulay, Vincent
Carracedo, Ángel
Journal: American journal of human genetics
Citation: Salas, Antono et al., The Making of the African mtDNA Landscape, American journal of human genetics , 71(5), 2002, pp. 1082-1111
Authors:
Verrelli, Brian C.
McDonald, John H.
Argyropoulos, George
Destro-Bisol, Giovanni
Froment, Alain
Drousiotou, Anthi
Lefranc, Gerard
Helal, Ahmed N.
Loiselet, Jacques
Tishkoff, Sarah A.
Journal: American journal of human genetics
Citation: C. Verrelli, Brian et al., Evidence for Balancing Selection from Nucleotide Sequence Analyses of Human G6PD, American journal of human genetics , 71(5), 2002, pp. 1112-1128
Authors:
Lin, Shin
Cutler, David J.
Zwick, Michael E.
Chakravarti, Aravinda
Journal: American journal of human genetics
Citation: Lin, Shin et al., Haplotype Inference in Random Population Samples, American journal of human genetics , 71(5), 2002, pp. 1129-1137
Authors:
Crolla, John A.
Heyningen, Veronica, Van
Journal: American journal of human genetics
Citation: A. Crolla, John et Heyningen, Veronica, Van, Frequent Chromosome Aberrations Revealed by Molecular Cytogenetic Studies in Patients with Aniridia, American journal of human genetics , 71(5), 2002, pp. 1138-1149
Authors:
Bandelt, Hans-Jürgen
Quintana-Murci, Lluìs
Salas, Antonio
Macaulay, Vincent
Journal: American journal of human genetics
Citation: Bandelt, Hans-jürgen et al., The Fingerprint of Phantom Mutations in Mitochondrial DNA Data, American journal of human genetics , 71(5), 2002, pp. 1150-1160
Authors:
Otto, Edgar
Hoefele, Julia
Ruf, Rainer
Mueller, Adelheid M.
Hiller, Karl S.
Wolf, Matthias T.F.
Schuermann, Maria J.
Becker, Achim
Birkenhäger, Ralf
Sudbrak, Ralf
Hennies, Hans C.
Nürnberg, Peter
Hildebrandt, Friedhelm
Journal: American journal of human genetics
Citation: Otto, Edgar et al., A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution, American journal of human genetics , 71(5), 2002, pp. 1161-1167
Authors:
Shahbazian, Mona D.
Zoghbi, Huda Y.
Journal: American journal of human genetics
Citation: D. Shahbazian, Mona et Y. Zoghbi, Huda, Rett Syndrome and MeCP2: Linking Epigenetics and Neuronal Function, American journal of human genetics , 71(6), 2002, pp. 1259-1272
Authors:
Stead, Johmn D.H.
Jeffreys, Alec J.
Journal: American journal of human genetics
Citation: Stead, Johmn D.h et J. Jeffreys, Alec, Structural Analysis of Insulin Minisatellite Alleles Reveals Unusually Large Differences in Diversity between Africans and Non-Africans, American journal of human genetics , 71(6), 2002, pp. 1273-1284
Authors:
Sànchez-Corral, Pilar
Pérez-Caballero, David
Huarte, Olatz
Simckes, Ari M.
Goicoechea, Elena
López-Trascasa, Margarita
Rodríguez de Córdoba, Santiago
Journal: American journal of human genetics
Citation: Sànchez-corral, Pilar et al., Structural and Functional Characterization of Factor H Mutations Associated with Atypical Hemolytic Uremic Syndrome, American journal of human genetics , 71(6), 2002, pp. 1285-1295
Authors:
Shifman, Sagiv
Bronstein, Michal
Sternfeld, Meira
Pisanté-Shalom, Anne
Lev-Lehman, Efrat
Weizman, Avraham
Reznik, Ilya
Spivak, Baruch
Grisaru, Nimrod
Karp, Leon
Schiffer, Richard
Kotler, Moshe
Strous, Rael D.",Swartz-Vanetik,"Knobler, Haim Y.
Shinar, Eilat
Beckmann, Jacques S.
Yakir, Benjamin
Risch, Neil
Zak, Naomi B.
Darvasi, Ariel
Journal: American journal of human genetics
Citation: Shifman, Sagiv et al., A Highly Significant Association between a COMT Haplotype and Schizophrenia, American journal of human genetics , 71(6), 2002, pp. 1296-1302