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Studies

44998 Unclassified

16794 Research

15990 Reviews

12050 Case Reports

6971 Other Trials

5473 Advanced Trials

2745 Early Trials

613 Meta-Analysis

Guidelines

176 Guidelines

99 Consensuses

95 Cochrane

Congresses

7604 Abstracts

1

Research

A polymorphic genomic duplication on human chromosome 15 is a susceptibility factor for panic and phobic disorders.

Gratacòs M, Nadal M, Martín-Santos R, Pujana M A, Gago J ...

Cell Vol 106(3)

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Date 10 Aug 2001

Institutional score
0.00
Impact
3197.10

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Date 10 Aug 2001

Institutional score
0.00
Impact
3197.10
2

Research

Spontaneous inflammatory disease in transgenic rats expressing HLA-B27 and human beta 2m: an animal model of HLA-B27-associated human disorders.

Hammer R E, Maika S D, Richardson J A, Tang J P, Taurog J D

Cell Vol 63(5)

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Date 30 Nov 1990

Institutional score
35.25
Impact
3197.10

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Date 30 Nov 1990

Institutional score
35.25
Impact
3197.10
3

Research

Cryo-EM Structure of Chikungunya Virus in Complex with the Mxra8 Receptor.

Basore Katherine, Kim Arthur S, Nelson Christopher A, Zhang Rong, Smith Brittany K ...

Cell Vol 177(7)

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Date 13 Jun 2019

Institutional score
0.00
Impact
3197.10

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Date 13 Jun 2019

Institutional score
0.00
Impact
3197.10
4

Research

Organ-specific disease provoked by systemic autoimmunity.

Kouskoff V, Korganow A S, Duchatelle V, Degott C, Benoist C ...

Cell Vol 87(5)

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Date 29 Nov 1996

Institutional score
0.00
Impact
3197.10

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Date 29 Nov 1996

Institutional score
0.00
Impact
3197.10
5

Research

CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.

Marcelino J, Carpten J D, Suwairi W M, Gutierrez O M, Schwartz S ...

Nature genetics Vol 23(3)

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Date 01 Nov 1999

Institutional score
13.14
Impact
2459.31

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Date 01 Nov 1999

Institutional score
13.14
Impact
2459.31
6

Research

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development.

Cappello Silvia, Gray Mary J, Badouel Caroline, Lange Simona, Einsiedler Melanie ...

Nature genetics Vol 45(11)

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Date 01 Nov 2013

Institutional score
0.00
Impact
2459.31

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Date 01 Nov 2013

Institutional score
0.00
Impact
2459.31
7

Research

Mutations in TRPV4 cause an inherited arthropathy of hands and feet.

Lamandé Shireen R, Yuan Yuan, Gresshoff Irma L, Rowley Lynn, Belluoccio Daniele ...

Nature genetics Vol 43(11)

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Date 02 Oct 2011

Institutional score
0.00
Impact
2459.31

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Date 02 Oct 2011

Institutional score
0.00
Impact
2459.31
8

Research

Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.

Lyons Jonathan J, Yu Xiaomin, Hughes Jason D, Le Quang T, Jamil Ali ...

Nature genetics Vol 48(12)

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Date 01 Dec 2016

Institutional score
73.64
Impact
2459.31

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Date 01 Dec 2016

Institutional score
73.64
Impact
2459.31
9

Research

CARD15 mutations in Blau syndrome.

Miceli-Richard C, Lesage S, Rybojad M, Prieur A M, Manouvrier-Hanu S ...

Nature genetics Vol 29(1)

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Date 01 Sep 2001

Institutional score
0.00
Impact
2459.31

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Date 01 Sep 2001

Institutional score
0.00
Impact
2459.31
10

Research

Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.

Le Goff Carine, Mahaut Clémentine, Abhyankar Avinash, Le Goff Wilfried, Serre Valérie ...

Nature genetics Vol 44(1)

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Date 11 Dec 2011

Institutional score
0.00
Impact
2459.31

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Date 11 Dec 2011

Institutional score
0.00
Impact
2459.31

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