Accueil
Dervla M Connaughton
Dervla M Connaughton
Affiliations
Division of Nephrology.
Publications (24)
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
Journal of the American Society of Nephrology : JASN
Avec:
Nina Mann
,
Daniela A Braun
,
Kassaundra Amann
,
Weizhen Tan
,
Shirlee Shril
,
Dervla M Connaughton
,
Makiko Nakayama
,
Ronen Schneider
,
Thomas M Kitzler
,
Amelie T van der Ven
,
Jing Chen
,
Hadas Ityel
,
Asaf Vivante
,
Amar J Majmundar
,
Ankana Daga
,
Jillian K Warejko
,
Svjetlana Lovric
,
Shazia Ashraf
,
Tilman Jobst-Schwan
,
Eugen Widmeier
,
Hannah Hugo
,
Shrikant M Mane
,
Leslie Spaneas
,
Michael J G Somers
,
Michael A Ferguson
,
Avram Z Traum
,
Deborah R Stein
,
Michelle A Baum
,
Ghaleb H Daouk
,
Richard P Lifton
,
Shannon Manzi
,
Khashayar Vakili
,
Heung Bae Kim
,
Nancy M Rodig
,
Friedhelm Hildebrandt
Monogenic causes of chronic kidney disease in adults.
Kidney international
Avec:
Dervla M Connaughton
,
Claire Kennedy
,
Shirlee Shril
,
Nina Mann
,
Susan L Murray
,
Patrick A Williams
,
Eoin Conlon
,
Makiko Nakayama
,
Amelie T van der Ven
,
Hadas Ityel
,
Franziska Kause
,
Caroline M Kolvenbach
,
Rufeng Dai
,
Asaf Vivante
,
Daniela A Braun
,
Ronen Schneider
,
Thomas M Kitzler
,
Brona Moloney
,
Conor P Moran
,
John S Smyth
,
Alan Kennedy
,
Katherine Benson
,
Caragh Stapleton
,
Mark Denton
,
Colm Magee
,
Conall M O'Seaghdha
,
William D Plant
,
Matthew D Griffin
,
Atif Awan
,
Clodagh Sweeney
,
Shrikant M Mane
,
Richard P Lifton
,
Brenda Griffin
,
Sean Leavey
,
Liam Casserly
,
Declan G de Freitas
,
John Holian
,
Anthony Dorman
,
Brendan Doyle
,
Peter J Lavin
,
Mark A Little
,
Peter J Conlon
,
Friedhelm Hildebrandt
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.
American journal of medical genetics. Part A
Avec:
Bixia Zheng
,
Chunyan Wang
,
Steve Seltzsam
,
Sophia Schneider
,
Luca Schierbaum
,
Wilfred Wu
,
Rufeng Dai
,
Dervla M Connaughton
,
Makiko Nakayama
,
Nina Mann
,
Stuart B Bauer
,
Hazem S Awad
,
Loai A Eid
,
Velibor Tasic
,
Shirlee Shril
,
Friedhelm Hildebrandt
Personalized medicine in chronic kidney disease by detection of monogenic mutations.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Avec:
Dervla M Connaughton
,
Friedhelm Hildebrandt
Karyomegalic Interstitial Nephritis: Cancer Risk Following Transplantation.
Nephron
Avec:
Susan L Murray
,
Dervla M Connaughton
,
Neil K Fennelly
,
Elaine W Kay
,
Anthony Dorman
,
Brendan Doyle
,
Peter J Conlon
Utility of Genomic Testing after Renal Biopsy.
American journal of nephrology
Avec:
Susan L Murray
,
Anthony Dorman
,
Katherine A Benson
,
Dervla M Connaughton
,
Caragh P Stapleton
,
Neil K Fennelly
,
Claire Kennedy
,
Ciara A McDonnell
,
Kendrah Kidd
,
Sarah M Cormican
,
Louise A Ryan
,
Peter Lavin
,
Mark A Little
,
Anthony J Bleyer
,
Brendan Doyle
,
Gianpiero L Cavalleri
,
Friedhelm Hildebrandt
,
Peter J Conlon
DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation.
American journal of human genetics
Avec:
Ronen Schneider
,
Konstantin Deutsch
,
Gregory J Hoeprich
,
Jonathan Marquez
,
Tobias Hermle
,
Daniela A Braun
,
Steve Seltzsam
,
Thomas M Kitzler
,
Youying Mao
,
Florian Buerger
,
Amar J Majmundar
,
Ana C Onuchic-Whitford
,
Caroline M Kolvenbach
,
Luca Schierbaum
,
Sophia Schneider
,
Abdul A Halawi
,
Makiko Nakayama
,
Nina Mann
,
Dervla M Connaughton
,
Verena Klämbt
,
Matias Wagner
,
Korbinian M Riedhammer
,
Lutz Renders
,
Yoshichika Katsura
,
Dean Thumkeo
,
Neveen A Soliman
,
Shrikant Mane
,
Richard P Lifton
,
Shirlee Shril
,
Mustafa K Khokha
,
Julia Hoefele
,
Bruce L Goode
,
Friedhelm Hildebrandt
The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene Project.
Journal of nephrology
Avec:
Elhussein A E Elhassan
,
Susan L Murray
,
Dervla M Connaughton
,
Claire Kennedy
,
Sarah Cormican
,
Cliona Cowhig
,
Caragh Stapleton
,
Mark A Little
,
Kendrah Kidd
,
Anthony J Bleyer
,
Martina Živná
,
Stanislav Kmoch
,
Neil K Fennelly
,
Brendan Doyle
,
Anthony Dorman
,
Matthew D Griffin
,
Liam Casserly
,
Peter C Harris
,
Friedhelm Hildebrandt
,
Gianpiero L Cavalleri
,
Katherine A Benson
,
Peter J Conlon
Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tract American Journal of Medical Genetics Part C.
American journal of medical genetics. Part C, Seminars in medical genetics
Avec:
Dervla M Connaughton
,
Friedhelm Hildebrandt
Reclassification of Genetic Testing Results: A Case Report Demonstrating the Need for Structured Re-Evaluation of Genetic Findings.
Canadian journal of kidney health and disease
Avec:
Clara Schott
,
Samantha Colaiacovo
,
Cadence Baker
,
Matthew A Weir
,
Dervla M Connaughton
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT).
Genetics in medicine : official journal of the American College of Medical Genetics
Avec:
Chen-Han Wilfred Wu
,
Nina Mann
,
Makiko Nakayama
,
Dervla M Connaughton
,
Rufeng Dai
,
Caroline M Kolvenbach
,
Franziska Kause
,
Isabel Ottlewski
,
Chunyan Wang
,
Verena Klämbt
,
Steve Seltzsam
,
Ethan W Lai
,
Aravind Selvin
,
Prabha Senguttuva
,
Olaf Bodamer
,
Deborah R Stein
,
Sherif El Desoky
,
Jameela A Kari
,
Velibor Tasic
,
Stuart B Bauer
,
Shirlee Shril
,
Friedhelm Hildebrandt
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
American journal of human genetics
Avec:
Dervla M Connaughton
,
Rufeng Dai
,
Danielle J Owen
,
Jonathan Marquez
,
Nina Mann
,
Adda L Graham-Paquin
,
Makiko Nakayama
,
Etienne Coyaud
,
Estelle M N Laurent
,
Jonathan R St-Germain
,
Lot Snijders Blok
,
Arianna Vino
,
Verena Klämbt
,
Konstantin Deutsch
,
Chen-Han Wilfred Wu
,
Caroline M Kolvenbach
,
Franziska Kause
,
Isabel Ottlewski
,
Ronen Schneider
,
Thomas M Kitzler
,
Amar J Majmundar
,
Florian Buerger
,
Ana C Onuchic-Whitford
,
Mao Youying
,
Amy Kolb
,
Daanya Salmanullah
,
Evan Chen
,
Amelie T van der Ven
,
Jia Rao
,
Hadas Ityel
,
Steve Seltzsam
,
Johanna M Rieke
,
Jing Chen
,
Asaf Vivante
,
Daw-Yang Hwang
,
Stefan Kohl
,
Gabriel C Dworschak
,
Tobias Hermle
,
Mariëlle Alders
,
Tobias Bartolomaeus
,
Stuart B Bauer
,
Michelle A Baum
,
Eva H Brilstra
,
Thomas D Challman
,
Jacob Zyskind
,
Carrie E Costin
,
Katrina M Dipple
,
Floor A Duijkers
,
Marcia Ferguson
,
David R Fitzpatrick
,
Roger Fick
,
Ian A Glass
,
Peter J Hulick
,
Antonie D Kline
,
Ilona Krey
,
Selvin Kumar
,
Weining Lu
,
Elysa J Marco
,
Ingrid M Wentzensen
,
Heather C Mefford
,
Konrad Platzer
,
Inna S Povolotskaya
,
Juliann M Savatt
,
Natalia V Shcherbakova
,
Prabha Senguttuvan
,
Audrey E Squire
,
Deborah R Stein
,
Isabelle Thiffault
,
Victoria Y Voinova
,
Michael J G Somers
,
Michael A Ferguson
,
Avram Z Traum
,
Ghaleb H Daouk
,
Ankana Daga
,
Nancy M Rodig
,
Paulien A Terhal
,
Ellen van Binsbergen
,
Loai A Eid
,
Velibor Tasic
,
Hila Milo Rasouly
,
Tze Y Lim
,
Dina F Ahram
,
Ali G Gharavi
,
Heiko M Reutter
,
Heidi L Rehm
,
Daniel G MacArthur
,
Monkol Lek
,
Kristen M Laricchia
,
Richard P Lifton
,
Hong Xu
,
Shrikant M Mane
,
Simone Sanna-Cherchi
,
Andrew D Sharrocks
,
Brian Raught
,
Simon E Fisher
,
Maxime Bouchard
,
Mustafa K Khokha
,
Shirlee Shril
,
Friedhelm Hildebrandt
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations.
American journal of human genetics
Avec:
Nina Mann
,
Franziska Kause
,
Erik K Henze
,
Anant Gharpure
,
Shirlee Shril
,
Dervla M Connaughton
,
Makiko Nakayama
,
Verena Klämbt
,
Amar J Majmundar
,
Chen-Han W Wu
,
Caroline M Kolvenbach
,
Rufeng Dai
,
Jing Chen
,
Amelie T van der Ven
,
Hadas Ityel
,
Madeleine J Tooley
,
Jameela A Kari
,
Lucy Bownass
,
Sherif El Desoky
,
Elisa De Franco
,
Mohamed Shalaby
,
Velibor Tasic
,
Stuart B Bauer
,
Richard S Lee
,
Jonathan M Beckel
,
Weiqun Yu
,
Shrikant M Mane
,
Richard P Lifton
,
Heiko Reutter
,
Sian Ellard
,
Ryan E Hibbs
,
Toshimitsu Kawate
,
Friedhelm Hildebrandt
Potential Pitfalls in Pre-implantation Genetic Diagnosis in a Patient with Tuberous Sclerosis and Isolated Mosaicism for a
Molecular syndromology
Avec:
Kristin M Ikeda
,
Andrew A House
,
Dervla M Connaughton
,
Stephen E Pautler
,
Victoria Mok Siu
,
Michelle-Lee Jones
Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes.
American journal of medical genetics. Part A
Avec:
Caroline M Kolvenbach
,
Amelie T van der Ven
,
Franziska Kause
,
Shirlee Shril
,
Marcello Scala
,
Dervla M Connaughton
,
Nina Mann
,
Makiko Nakayama
,
Rufeng Dai
,
Thomas M Kitzler
,
Ronen Schneider
,
Luca Schierbaum
,
Sophia Schneider
,
Andrea Accogli
,
Annalaura Torella
,
Gianluca Piatelli
,
Vincenzo Nigro
,
Valeria Capra
,
Bernd Hoppe
,
Stefanie Märzheuser
,
Eberhard Schmiedeke
,
Heidi L Rehm
,
Shrikant Mane
,
Richard P Lifton
,
Gabriel C Dworschak
,
Alina C Hilger
,
Heiko Reutter
,
Friedhelm Hildebrandt
Proteomic analysis identifies ZMYM2 as endogenous binding partner of TBX18 protein in 293 and A549 cells.
The Biochemical journal
Avec:
Timo H-W Lüdtke
,
Marc-Jens Kleppa
,
Reginaldo Rivera-Reyes
,
Fairouz Qasrawi
,
Dervla M Connaughton
,
Shirlee Shril
,
Friedhelm Hildebrandt
,
Andreas Kispert
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models.
American journal of medical genetics. Part A
Avec:
Chunyan Wang
,
Steve Seltzsam
,
Bixia Zheng
,
Chen-Han Wilfred Wu
,
Camille Nicolas-Frank
,
Kirollos Yousef
,
Kit Sing Au
,
Nina Mann
,
Dalia Pantel
,
Sophia Schneider
,
Luca Schierbaum
,
Thomas M Kitzler
,
Dervla M Connaughton
,
Youying Mao
,
Rufeng Dai
,
Makiko Nakayama
,
Jameela A Kari
,
Sherif El Desoky
,
Mohammed Shalaby
,
Loai A Eid
,
Hazem S Awad
,
Velibor Tasic
,
Shrikant M Mane
,
Richard P Lifton
,
Michelle A Baum
,
Shirlee Shril
,
Carlos R Estrada
,
Friedhelm Hildebrandt
Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal Kidney.
Nephron
Avec:
Luca M Schierbaum
,
Sophia Schneider
,
Florian Buerger
,
Abdul Aziz Halawi
,
Steve Seltzsam
,
Chunyan Wang
,
Bixia Zheng
,
Chen-Han Wilfried Wu
,
Rufeng Dai
,
Dervla M Connaughton
,
Daanya Salmanullah
,
Makiko Nakayama
,
Nina Mann
,
Shirlee Shril
,
Friedhelm Hildebrandt
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
Genetics in medicine : official journal of the American College of Medical Genetics
Avec:
Steve Seltzsam
,
Chunyan Wang
,
Bixia Zheng
,
Nina Mann
,
Dervla M Connaughton
,
Chen-Han Wilfred Wu
,
Sophia Schneider
,
Luca Schierbaum
,
Franziska Kause
,
Caroline M Kolvenbach
,
Makiko Nakayama
,
Rufeng Dai
,
Isabel Ottlewski
,
Ronen Schneider
,
Konstantin Deutsch
,
Florian Buerger
,
Verena Klämbt
,
Youying Mao
,
Ana C Onuchic-Whitford
,
Camille Nicolas-Frank
,
Kirollos Yousef
,
Dalia Pantel
,
Ethan W Lai
,
Daanya Salmanullah
,
Amar J Majmundar
,
Stuart B Bauer
,
Nancy M Rodig
,
Michael J G Somers
,
Avram Z Traum
,
Deborah R Stein
,
Ankana Daga
,
Michelle A Baum
,
Ghaleb H Daouk
,
Velibor Tasic
,
Hazem S Awad
,
Loai A Eid
,
Sherif El Desoky
,
Mohammed Shalaby
,
Jameela A Kari
,
Hanan M Fathy
,
Neveen A Soliman
,
Shrikant M Mane
,
Shirlee Shril
,
Michael A Ferguson
,
Friedhelm Hildebrandt
Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Avec:
Bixia Zheng
,
Steve Seltzsam
,
Chunyan Wang
,
Luca Schierbaum
,
Sophia Schneider
,
Chen-Han Wilfred Wu
,
Rufeng Dai
,
Dervla M Connaughton
,
Makiko Nakayama
,
Nina Mann
,
Natasa Stajic
,
Shrikant Mane
,
Stuart B Bauer
,
Velibor Tasic
,
Hyun Joo Nam
,
Shirlee Shril
,
Friedhelm Hildebrandt
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
European urology open science
Avec:
Chen-Han Wilfred Wu
,
Tze Y Lim
,
Chunyan Wang
,
Steve Seltzsam
,
Bixia Zheng
,
Luca Schierbaum
,
Sophia Schneider
,
Nina Mann
,
Dervla M Connaughton
,
Makiko Nakayama
,
Amelie T van der Ven
,
Rufeng Dai
,
Caroline M Kolvenbach
,
Franziska Kause
,
Isabel Ottlewski
,
Natasa Stajic
,
Neveen A Soliman
,
Jameela A Kari
,
Sherif El Desoky
,
Hanan M Fathy
,
Danko Milosevic
,
Daniel Turudic
,
Muna Al Saffar
,
Hazem S Awad
,
Loai A Eid
,
Aravind Ramanathan
,
Prabha Senguttuvan
,
Shrikant M Mane
,
Richard S Lee
,
Stuart B Bauer
,
Weining Lu
,
Alina C Hilger
,
Velibor Tasic
,
Shirlee Shril
,
Simone Sanna-Cherchi
,
Friedhelm Hildebrandt
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.
Human genetics
Avec:
Thomas M Kitzler
,
Ronen Schneider
,
Stefan Kohl
,
Caroline M Kolvenbach
,
Dervla M Connaughton
,
Rufeng Dai
,
Nina Mann
,
Makiko Nakayama
,
Amar J Majmundar
,
Chen-Han W Wu
,
Jameela A Kari
,
Sherif M El Desoky
,
Prabha Senguttuvan
,
Radovan Bogdanovic
,
Natasa Stajic
,
Zaheer Valivullah
,
Monkol Lek
,
Shrikant Mane
,
Richard P Lifton
,
Velibor Tasic
,
Shirlee Shril
,
Friedhelm Hildebrandt
Renal transplant outcomes in patients with autosomal dominant tubulointerstitial kidney disease.
Clinical transplantation
Avec:
Sarah Cormican
,
Claire Kennedy
,
Dervla M Connaughton
,
Patrick O'Kelly
,
Susan Murray
,
Martina Živná
,
Stanislav Kmoch
,
Neil K Fennelly
,
Katherine A Benson
,
Eoin T Conlon
,
Gianpiero L Cavalleri
,
Claire Foley
,
Brendan Doyle
,
Anthony Dorman
,
Mark A Little
,
Peter Lavin
,
Kendrah Kidd
,
Anthony J Bleyer
,
Peter J Conlon
An Exome Sequencing Study of 10 Families with IgA Nephropathy.
Nephron
Avec:
Caragh P Stapleton
,
Claire Kennedy
,
Neil K Fennelly
,
Susan L Murray
,
Dervla M Connaughton
,
Anthony M Dorman
,
Brendan Doyle
,
Gianpiero L Cavalleri
,
Peter J Conlon
Réseau de co-auteurs
Friedhelm Hildebrandt
19 collaborations
Shirlee Shril
15 collaborations
Nina Mann
14 collaborations
Makiko Nakayama
14 collaborations
Rufeng Dai
12 collaborations
Caroline M Kolvenbach
9 collaborations
Steve Seltzsam
9 collaborations
Velibor Tasic
9 collaborations
Richard P Lifton
8 collaborations
Sophia Schneider
8 collaborations
Ronen Schneider
7 collaborations
Thomas M Kitzler
7 collaborations
Shrikant M Mane
7 collaborations
Franziska Kause
7 collaborations
Chunyan Wang
7 collaborations
Luca Schierbaum
7 collaborations
Stuart B Bauer
7 collaborations
Amelie T van der Ven
6 collaborations
Amar J Majmundar
6 collaborations
Brendan Doyle
6 collaborations
Peter J Conlon
6 collaborations
Bixia Zheng
6 collaborations
Chen-Han Wilfred Wu
6 collaborations
Jameela A Kari
6 collaborations
Claire Kennedy
5 collaborations
Susan L Murray
5 collaborations
Anthony Dorman
5 collaborations
Loai A Eid
5 collaborations
Neil K Fennelly
5 collaborations
Verena Klämbt
5 collaborations
Sherif El Desoky
5 collaborations
Hadas Ityel
4 collaborations
Deborah R Stein
4 collaborations
Michelle A Baum
4 collaborations
Mark A Little
4 collaborations
Hazem S Awad
4 collaborations
Gianpiero L Cavalleri
4 collaborations
Florian Buerger
4 collaborations
Shrikant Mane
4 collaborations
Isabel Ottlewski
4 collaborations
Daniela A Braun
3 collaborations
Jing Chen
3 collaborations
Asaf Vivante
3 collaborations
Ankana Daga
3 collaborations
Michael J G Somers
3 collaborations
Michael A Ferguson
3 collaborations
Avram Z Traum
3 collaborations
Ghaleb H Daouk
3 collaborations
Nancy M Rodig
3 collaborations
Katherine A Benson
3 collaborations
Kendrah Kidd
3 collaborations
Anthony J Bleyer
3 collaborations
Konstantin Deutsch
3 collaborations
Youying Mao
3 collaborations
Ana C Onuchic-Whitford
3 collaborations
Neveen A Soliman
3 collaborations
Daanya Salmanullah
3 collaborations
Prabha Senguttuvan
3 collaborations
Natasa Stajic
3 collaborations
Caragh Stapleton
2 collaborations
Matthew D Griffin
2 collaborations
Liam Casserly
2 collaborations
Caragh P Stapleton
2 collaborations
Peter Lavin
2 collaborations
Jonathan Marquez
2 collaborations
Tobias Hermle
2 collaborations
Mustafa K Khokha
2 collaborations
Sarah Cormican
2 collaborations
Martina Živná
2 collaborations
Stanislav Kmoch
2 collaborations
Ethan W Lai
2 collaborations
Stefan Kohl
2 collaborations
Gabriel C Dworschak
2 collaborations
Weining Lu
2 collaborations
Tze Y Lim
2 collaborations
Heidi L Rehm
2 collaborations
Monkol Lek
2 collaborations
Simone Sanna-Cherchi
2 collaborations
Chen-Han W Wu
2 collaborations
Richard S Lee
2 collaborations
Heiko Reutter
2 collaborations
Alina C Hilger
2 collaborations
Camille Nicolas-Frank
2 collaborations
Kirollos Yousef
2 collaborations
Dalia Pantel
2 collaborations
Mohammed Shalaby
2 collaborations
Hanan M Fathy
2 collaborations
Kassaundra Amann
1 collaboration
Weizhen Tan
1 collaboration
Jillian K Warejko
1 collaboration
Svjetlana Lovric
1 collaboration
Shazia Ashraf
1 collaboration
Tilman Jobst-Schwan
1 collaboration
Eugen Widmeier
1 collaboration
Hannah Hugo
1 collaboration
Leslie Spaneas
1 collaboration
Shannon Manzi
1 collaboration
Khashayar Vakili
1 collaboration
Heung Bae Kim
1 collaboration
Patrick A Williams
1 collaboration
Eoin Conlon
1 collaboration
Brona Moloney
1 collaboration
Conor P Moran
1 collaboration
John S Smyth
1 collaboration
Alan Kennedy
1 collaboration
Katherine Benson
1 collaboration
Mark Denton
1 collaboration
Colm Magee
1 collaboration
Conall M O'Seaghdha
1 collaboration
William D Plant
1 collaboration
Atif Awan
1 collaboration
Clodagh Sweeney
1 collaboration
Brenda Griffin
1 collaboration
Sean Leavey
1 collaboration
Declan G de Freitas
1 collaboration
John Holian
1 collaboration
Peter J Lavin
1 collaboration
Wilfred Wu
1 collaboration
Elaine W Kay
1 collaboration
Ciara A McDonnell
1 collaboration
Sarah M Cormican
1 collaboration
Louise A Ryan
1 collaboration
Gregory J Hoeprich
1 collaboration
Abdul A Halawi
1 collaboration
Matias Wagner
1 collaboration
Korbinian M Riedhammer
1 collaboration
Lutz Renders
1 collaboration
Yoshichika Katsura
1 collaboration
Dean Thumkeo
1 collaboration
Julia Hoefele
1 collaboration
Bruce L Goode
1 collaboration
Elhussein A E Elhassan
1 collaboration
Cliona Cowhig
1 collaboration
Peter C Harris
1 collaboration
Clara Schott
1 collaboration
Samantha Colaiacovo
1 collaboration
Cadence Baker
1 collaboration
Matthew A Weir
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Aravind Selvin
1 collaboration
Prabha Senguttuva
1 collaboration
Olaf Bodamer
1 collaboration
Danielle J Owen
1 collaboration
Adda L Graham-Paquin
1 collaboration
Etienne Coyaud
1 collaboration
Estelle M N Laurent
1 collaboration
Jonathan R St-Germain
1 collaboration
Lot Snijders Blok
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Arianna Vino
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Mao Youying
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Amy Kolb
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Evan Chen
1 collaboration
Jia Rao
1 collaboration
Johanna M Rieke
1 collaboration
Daw-Yang Hwang
1 collaboration
Mariëlle Alders
1 collaboration
Tobias Bartolomaeus
1 collaboration
Eva H Brilstra
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Thomas D Challman
1 collaboration
Jacob Zyskind
1 collaboration
Carrie E Costin
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Katrina M Dipple
1 collaboration
Floor A Duijkers
1 collaboration
Marcia Ferguson
1 collaboration
David R Fitzpatrick
1 collaboration
Roger Fick
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Ian A Glass
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Peter J Hulick
1 collaboration
Antonie D Kline
1 collaboration
Ilona Krey
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Selvin Kumar
1 collaboration
Elysa J Marco
1 collaboration
Ingrid M Wentzensen
1 collaboration
Heather C Mefford
1 collaboration
Konrad Platzer
1 collaboration
Inna S Povolotskaya
1 collaboration
Juliann M Savatt
1 collaboration
Natalia V Shcherbakova
1 collaboration
Audrey E Squire
1 collaboration
Isabelle Thiffault
1 collaboration
Victoria Y Voinova
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Paulien A Terhal
1 collaboration
Ellen van Binsbergen
1 collaboration
Hila Milo Rasouly
1 collaboration
Dina F Ahram
1 collaboration
Ali G Gharavi
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Heiko M Reutter
1 collaboration
Daniel G MacArthur
1 collaboration
Kristen M Laricchia
1 collaboration
Hong Xu
1 collaboration
Andrew D Sharrocks
1 collaboration
Brian Raught
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Simon E Fisher
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Maxime Bouchard
1 collaboration
Erik K Henze
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Lucy Bownass
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Elisa De Franco
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Weiqun Yu
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Sian Ellard
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Kristin M Ikeda
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Andrew A House
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Stephen E Pautler
1 collaboration
Victoria Mok Siu
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Michelle-Lee Jones
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Marcello Scala
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1 collaboration
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1 collaboration
Bernd Hoppe
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Stefanie Märzheuser
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Eberhard Schmiedeke
1 collaboration
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1 collaboration
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1 collaboration
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Fairouz Qasrawi
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Anthony M Dorman
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