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Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.
78 auth.
R. Segurado,
S. Detera-Wadleigh,
D. Levinson,
C. Lewis,
M. Gill,
J. Nurnberger,
N. Craddock,
J. DePaulo,
M. Baron,
E. Gershon,
J. Ekholm,
S. Cichon,
G. Turecki,
S. Claes,
J. Kelsoe,
...
P. Schofield,
R. F. Badenhop,
J. Morissette,
H. Coon,
D. Blackwood,
L. McInnes,
T. Foroud,
H. Edenberg,
T. Reich,
J. Rice,
A. Goate,
M. McInnis,
F. McMahon,
J. Badner,
L. Goldin,
P. Bennett,
V. Willour,
P. Zandi,
Jianjun Liu,
C. Gilliam,
S. Juo,
W. Berrettini,
T. Yoshikawa,
L. Peltonen,
J. Lönnqvist,
M. Nöthen,
J. Schumacher,
C. Windemuth,
M. Rietschel,
P. Propping,
W. Maier,
M. Alda,
P. Grof,
G. Rouleau,
J. Del-Favero,
C. van Broeckhoven,
J. Mendlewicz,
R. Adolfsson,
M. Spence,
H. Luebbert,
L. Adams,
J. Donald,
P. Mitchell,
N. Barden,
E. Shink,
W. Byerley,
W. Muir,
P. Visscher,
S. Macgregor,
H. Gurling,
G. Kalsi,
A. McQuillin,
M. Escamilla,
V. Reus,
P. León,
N. Freimer,
H. Ewald,
T. Kruse,
O. Mors,
U. Radhakrishna,
J. Blouin,
S. Antonarakis,
N. Akarsu
|
9 |
2003 |
9
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Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
28 auth.
J. Blouin,
B. Dombroski,
S. Nath,
V. Lasseter,
P. Wolyniec,
G. Nestadt,
M. Thornquist,
Gail Ullrich,
J. Mcgrath,
L. Kasch,
M. Lamacz,
M. Thomas,
C. Gehrig,
U. Radhakrishna,
S. E. Snyder,
...
Katherine Balk,
K. Neufeld,
K. Swartz,
N. deMarchi,
G. Papadimitriou,
D. Dikeos,
C. Stefanis,
A. Chakravarti,
B. Childs,
D. Housman,
H. Kazazian,
S. Antonarakis,
A. Pulver
|
9 |
1998 |
9
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|
|
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Mutations in GJB6 cause hidrotic ectodermal dysplasia
20 auth.
J. Lamartine,
Guilherme Munhoz Essenfelder,
Z. Kibar,
I. Lanneluc,
Edwige Callouet,
D. Laoudj,
G. Lemaître,
Colette Hand,
S. Hayflick,
J. Zonana,
...
S. Antonarakis,
U. Radhakrishna,
D. Kelsell,
A. Christianson,
A. Pitaval,
V. Kaloustian,
Clarke Fraser,
C. Blanchet‐Bardon,
G. Rouleau,
G. Waksman
|
8 |
2000 |
8
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|
|
🐜
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Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness
23 auth.
Hamish Scott,
Hamish Scott,
J. Kudoh,
M. Wattenhofer,
K. Shibuya,
A. Berry,
R. Chrast,
M. Guipponi,
Jun Wang,
K. Kawasaki,
...
S. Asakawa,
S. Minoshima,
F. Younus,
S. Mehdi,
U. Radhakrishna,
M. Papasavvas,
C. Gehrig,
C. Rossier,
M. Korostishevsky,
A. Gal,
N. Shimizu,
B. Bonné-Tamir,
S. Antonarakis
|
7 |
2001 |
7
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|
|
🐜
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Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1.
16 auth.
A. Bashamboo,
B. Ferraz-de-Souza,
D. Lourenço,
Lin Lin,
N. Sebire,
D. Montjean,
J. Bignon-Topalovic,
J. Mandelbaum,
J. Siffroi,
S. Christin‐Maitre,
...
U. Radhakrishna,
H. Rouba,
C. Ravel,
J. Seeler,
J. Achermann,
K. McElreavey
|
7 |
2010 |
7
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|
|
🦁
|
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.
13 auth.
U. Radhakrishna,
D. Bornholdt,
Hamish Scott,
Uday C. Patel,
C. Rossier,
H. Engel,
A. Bottani,
Divya Chandal,
J. Blouin,
J. V. Solanki,
...
K. Grzeschik,
S. Antonarakis,
S. Antonarakis
|
7 |
1999 |
7
🦁
|
|
🦁
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Mutation in GLI3 in postaxial polydactyly type A
U. Radhakrishna,
A. Wild,
K. Grzeschik,
S. Antonarakis
|
7 |
1997 |
7
🦁
|
|
🐜
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Y-chromosome lineages trace diffusion of people and languages in southwestern Asia.
13 auth.
Lluís Quintana-Murci,
Csilla Krausz,
T. Zerjal,
S.Hamid Sayar,
Michael F. Hammer,
S. Mehdi,
Q. Ayub,
Raheel Qamar,
A. Mohyuddin,
U. Radhakrishna,
...
M. Jobling,
C. Tyler-Smith,
Ken McElreavey
|
7 |
2001 |
7
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|
|
🐜
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Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity
22 auth.
J. Blouin,
M. Meeks,
U. Radhakrishna,
A. Sainsbury,
C. Gehring,
Genevieve Duriaux Sail,
L. Bartoloni,
Dombi,
A. O'rawe,
A. Walne,
...
E. Chung,
B. Afzelius,
M. Armengot,
M. Jorissen,
DV Schidlow,
L. Maldergem,
H. Walt,
R. Gardiner,
D. Probst,
P. Guerne,
C. D. Delozier-Blanchet,
S. Antonarakis
|
7 |
1999 |
7
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|
|
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|
Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.
11 auth.
H. Mehenni,
J. Blouin,
U. Radhakrishna,
Shiv Shanker Bhardwaj,
Kamla Bhardwaj,
V. Dixit,
...
Kent F. Richards,
Ambrosio Bermejo-Fenoll,
António Leal,
Ranjan C. Raval,
S. Antonarakis
|
7 |
1997 |
7
🐜
|
|
🐜
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A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.
23 auth.
X. D. de Mollerat,
F. Gurrieri,
C. T. Morgan,
E. Sangiorgi,
D. Everman,
Paola Gaspari,
J. Amiel,
M. Bamshad,
R. Lyle,
J. Blouin,
...
J. Allanson,
B. Le Marec,
Melba Wilson,
N. Braverman,
U. Radhakrishna,
C. DeLozier-Blanchet,
A. Abbott,
V. Elghouzzi,
S. Antonarakis,
R. Stevenson,
A. Munnich,
G. Neri,
C. Schwartz
|
6 |
2003 |
6
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