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Studies

51676 Unclassified

21130 Reviews

21004 Case Reports

14398 Research

10395 Other Trials

8894 Advanced Trials

8860 Early Trials

754 Meta-Analysis

Guidelines

301 Guidelines

128 Consensuses

118 Cochrane

Congresses

12022 Abstracts

1

Research

Adrenergic Signaling in Muscularis Macrophages Limits Infection-Induced Neuronal Loss.

Matheis Fanny, Muller Paul A, Graves Christina L, Gabanyi Ilana, Kerner Zachary J ...

Cell Vol 180(1)

Read

Date 09 Jan 2020

Institutional score
39.66
Impact
3860.25

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Date 09 Jan 2020

Institutional score
39.66
Impact
3860.25
2

Research

An Airway Protection Program Revealed by Sweeping Genetic Control of Vagal Afferents.

Prescott Sara L, Umans Benjamin D, Williams Erika K, Brust Rachael D, Liberles Stephen D

Cell Vol 181(3)

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Date 30 Apr 2020

Institutional score
219.34
Impact
3860.25

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Date 30 Apr 2020

Institutional score
219.34
Impact
3860.25
3

Research

Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia.

Gockel Ines, Becker Jessica, Wouters Mira M, Niebisch Stefan, Gockel Henning R ...

Nature genetics Vol 46(8)

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Date 01 Aug 2014

Institutional score
89.61
Impact
2459.31

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Date 01 Aug 2014

Institutional score
89.61
Impact
2459.31
4

Research

Mutant WD-repeat protein in triple-A syndrome.

Tullio-Pelet A, Salomon R, Hadj-Rabia S, Mugnier C, de Laet M H ...

Nature genetics Vol 26(3)

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Date 01 Nov 2000

Institutional score
0.00
Impact
2459.31

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Date 01 Nov 2000

Institutional score
0.00
Impact
2459.31
5

Research

Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency.

Meimaridou Eirini, Kowalczyk Julia, Guasti Leonardo, Hughes Claire R, Wagner Florian ...

Nature genetics Vol 44(7)

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Date 27 May 2012

Institutional score
0.00
Impact
2459.31

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Date 27 May 2012

Institutional score
0.00
Impact
2459.31
6

Research

Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).

Logan Clare V, Lucke Barbara, Pottinger Caroline, Abdelhamed Zakia A, Parry David A ...

Nature genetics Vol 43(12)

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Date 20 Nov 2011

Institutional score
30.74
Impact
2459.31

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Date 20 Nov 2011

Institutional score
30.74
Impact
2459.31
7

Research

Keap1-null mutation leads to postnatal lethality due to constitutive Nrf2 activation.

Wakabayashi Nobunao, Itoh Ken, Wakabayashi Junko, Motohashi Hozumi, Noda Shuhei ...

Nature genetics Vol 35(3)

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Date 01 Nov 2003

Institutional score
16.20
Impact
2459.31

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Date 01 Nov 2003

Institutional score
16.20
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

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.

Quaderi N A, Schweiger S, Gaudenz K, Franco B, Rugarli E I ...

Nature genetics Vol 17(3)

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Date 01 Nov 1997

Institutional score
0.00
Impact
2459.31

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Date 01 Nov 1997

Institutional score
0.00
Impact
2459.31
10

Research

Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases.

Lenz Tobias L, Deutsch Aaron J, Han Buhm, Hu Xinli, Okada Yukinori ...

Nature genetics Vol 47(9)

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Date 01 Sep 2015

Institutional score
286.08
Impact
2459.31

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Date 01 Sep 2015

Institutional score
286.08
Impact
2459.31

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