Skip to main content
Features
Assistant
AI grounded in research
Search
Full-text citation search
Collections
Organize and monitor papers
All Features →
Integrations
MCP
Connect AI agents to Scite
API
Programmatic data access
Holdings
Full-text via your library
Zotero Plugin
Citation data in Zotero
Browser Extension
Citation badges anywhere
All Integrations →
Data
Rankings
Pricing
Log In
Start Free Trial
Features
Assistant
AI grounded in research
Search
Full-text citation search
Collections
Organize and monitor papers
All Features →
Integrations
MCP
Connect AI agents to Scite
API
Programmatic data access
Holdings
Full-text via your library
Zotero Plugin
Citation data in Zotero
Browser Extension
Citation badges anywhere
All Integrations →
Data
Rankings
Pricing
Log In
Start Free Trial
Martina Huemer
Sign up to set email alerts
172
Publications
6,604
Citation Statements Received
12,006
Citation Statements Given
How they've been cited
5,895
178
6,387
39
How they cite others
8,586
306
11,670
30
Affiliations
University Children's Hospital Zurich
,
University of Zurich
Publications
Order By: Most citations
Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
Baumgartner
1
,
Hörster
2
,
Dionisi‐Vici
3
et al.
2014
Orphanet J Rare Dis
Abstract
Show
759
14
962
3
Get access via publisher
Add to collection
Cite
Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision
Häberle
1
,
Burlina
2
,
Chakrapani
3
et al.
2019
J of Inher Metab Disea
Abstract
Show
539
12
717
2
Get access via publisher
Add to collection
Cite
Suggested guidelines for the diagnosis and management of urea cycle disorders
Häberle
1
,
Boddaert
2
,
Burlina
3
et al.
2012
Orphanet J Rare Dis
Abstract
Show
652
13
684
2
Get access via publisher
Add to collection
Cite
Guidelines for the diagnosis and management of cystathionine beta‐synthase deficiency
Morris
1
,
Kožich
2
,
Santra
3
et al.
2016
J of Inher Metab Disea
Abstract
Show
360
5
511
0
Get access via publisher
Add to collection
Cite
Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision
Forny
1
,
Hörster
2
,
Ballhausen
3
et al.
2021
J of Inher Metab Disea
Abstract
Show
309
1
390
0
2
Get access via publisher
Add to collection
Cite
Clinical presentation and outcome in a series of 88 patients with the cblC defect
Fischer
1
,
Huemer
2
,
Baumgartner
3
et al.
2014
J of Inher Metab Disea
Abstract
Show
183
8
211
2
Get access via publisher
Add to collection
Cite
Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy
Gai
1
,
Ghezzi
2
,
Johnson
3
et al.
2013
The American Journal of Human Genetics
Abstract
Show
182
8
196
1
Get access via publisher
Add to collection
Cite
Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines
Huemer
1
,
Kožich
2
,
Rinaldo
3
et al.
2015
J of Inher Metab Disea
Abstract
Show
146
6
156
0
Get access via publisher
Add to collection
Cite
1
2
3
4