Michael F Wangler

Affiliations
  • Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas, USA.
ORCID: 0000-0001-5245-5910

Publications (37)

ABCD1 and X-linked adrenoleukodystrophy: A disease with a markedly variable phenotype showing conserved neurobiology in animal models.

Journal of neuroscience research
Avec: Joshua Manor , Hyunglok Chung , Pranjali K Bhagwat , Michael F Wangler

An

Frontiers in cell and developmental biology
Avec: Rebecca Martinez-Moreno , Elisabet Selga , Helena Riuró , David Carreras , Mered Parnes , Chandra Srinivasan , Michael F Wangler , Guillermo J Pérez , Fabiana S Scornik , Ramon Brugada

MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia.

Annals of neurology
Avec: Linyan Meng , Pirjo Isohanni , Yunru Shao , Brett H Graham , Scott E Hickey , Stephanie Brooks , Anu Suomalainen , Pascal Joset , Katharina Steindl , Anita Rauch , Annette Hackenberg , Frances A High , Amy Armstrong-Javors , Niccolò E Mencacci , Paulina Gonzàlez-Latapi , Walaa A Kamel , Jasem Y Al-Hashel , Bernabé I Bustos , Alejandro V Hernandez , Dimitri Krainc , Steven J Lubbe , Hilde Van Esch , Chiara De Luca , Katleen Ballon , Claudia Ravelli , Lydie Burglen , Leila Qebibo , Daniel G Calame , Tadahiro Mitani , Dana Marafi , Davut Pehlivan , Nebal W Saadi , Yavuz Sahin , Reza Maroofian , Stephanie Efthymiou , Henry Houlden , Shazia Maqbool , Fatima Rahman , Shen Gu , Jennifer E Posey , James R Lupski , Jill V Hunter , Michael F Wangler , Christopher J Carroll , Yaping Yang

Novel CIC variants identified in individuals with neurodevelopmental phenotypes.

Human mutation
Avec: Saloni Sharma , Brenna Hourigan , Zain Patel , Jill A Rosenfeld , Katie M Chan , Michael F Wangler , Joanna S Yi , Anna Lehman , Auteur inconnu , Gabriella Horvath , Paul A Cloos , Qiumin Tan

Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability.

Proceedings of the National Academy of Sciences of the United States of America
Avec: Debdeep Dutta , Oguz Kanca , Rishi V Shridharan , Paul C Marcogliese , Benjamin Steger , Marie Morimoto , F Graeme Frost , Ellen Macnamara , Auteur inconnu , Michael F Wangler , Shinya Yamamoto , Andreas Jenny , David Adams , May C Malicdan , Hugo J Bellen

Dicarboxylic acylcarnitine biomarkers in peroxisome biogenesis disorders.

Molecular genetics and metabolism
Avec: Michael F Wangler , Barbara Lesko , Rejwi Dahal , Sharayu Jangam , Pradnya Bhadane , Theodore E Wilson , Molly McPheron , Marcus J Miller

Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans.

Nature reviews. Genetics
Avec: Shinya Yamamoto , Oguz Kanca , Michael F Wangler , Hugo J Bellen

AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders.

NEJM AI
Avec: Dongxue Mao , Chaozhong Liu , Linhua Wang , Rami Ai-Ouran , Cole Deisseroth , Sasidhar Pasupuleti , Seon Young Kim , Lucian Li , Jill A Rosenfeld , Linyan Meng , Lindsay C Burrage , Michael F Wangler , Shinya Yamamoto , Auteur inconnu , Michael Santana , Victor Perez , Priyank Shukla , Christine M Eng , Brendan Lee , Bo Yuan , Fan Xia , Hugo J Bellen , Pengfei Liu , Zhandong Liu

Genome sequencing analysis of a family with a child displaying severe abdominal distention and recurrent hypoglycemia.

Molecular genetics & genomic medicine
Avec: Jidong Liu , Guolian Ding , Kexin Zou , Ziru Jiang , Junyu Zhang , Yunhua Lu , Antonella Pignata , Eric Venner , Pengfei Liu , Zhandong Liu , Michael F Wangler , Zheng Sun

De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment.

Human molecular genetics
Avec: Debdeep Dutta , Lauren C Briere , Oguz Kanca , Paul C Marcogliese , Melissa A Walker , Frances A High , Adeline Vanderver , Joel Krier , Nikkola Carmichael , Christine Callahan , Ryan J Taft , Cas Simons , Guy Helman , Undiagnosed Diseases Network , Michael F Wangler , Shinya Yamamoto , David A Sweetser , Hugo J Bellen

Biases in arginine codon usage correlate with genetic disease risk.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Katharina V Schulze , Neil A Hanchard , Michael F Wangler

A Genetic Screen for Genes That Impact Peroxisomes in

G3 (Bethesda, Md.)
Avec: Hillary K Graves , Sharayu Jangam , Kai Li Tan , Antonella Pignata , Elaine S Seto , Shinya Yamamoto , Michael F Wangler

Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy.

Human mutation
Avec: Nurit Assia Batzir , Pranjali Kishor Bhagwat , Austin Larson , Zeynep Coban Akdemir , Maciej Bagłaj , Leon Bofferding , Katherine B Bosanko , Skander Bouassida , Bert Callewaert , Ashley Cannon , Yazmin Enchautegui Colon , Adolfo D Garnica , Margaret H Harr , Sandra Heck , Anna C E Hurst , Shalini N Jhangiani , Bertrand Isidor , Rebecca O Littlejohn , Pengfei Liu , Pilar Magoulas , Helen Mar Fan , Ronit Marom , Scott McLean , Marjan M Nezarati , Kimberly M Nugent , Michael B Petersen , Maria L Rocha , Elizabeth Roeder , Robert Smigiel , Ian Tully , James Weisfeld-Adams , Katerina O Wells , Auteur inconnu , Jennifer E Posey , James R Lupski , Arthur L Beaudet , Michael F Wangler

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila.

Journal of visualized experiments : JoVE
Avec: J Michael Harnish , Samantha L Deal , Hsiao-Tuan Chao , Michael F Wangler , Shinya Yamamoto

HGG advances
Avec: Michael M Khayat , Jianhong Hu , Yunyun Jiang , He Li , Varuna Chander , Moez Dawood , Adam W Hansen , Shoudong Li , Jennifer Friedman , Laura Cross , Emilia K Bijlsma , Claudia A L Ruivenkamp , Francis H Sansbury , Jeffrey W Innis , Jessica Omark O'Shea , Qingchang Meng , Jill A Rosenfeld , Kirsty McWalter , Michael F Wangler , James R Lupski , Jennifer E Posey , David Murdock , Richard A Gibbs

Rare deleterious de novo missense variants in Rnf2/Ring2 are associated with a neurodevelopmental disorder with unique clinical features.

Human molecular genetics
Avec: Xi Luo , Kelly Schoch , Sharayu V Jangam , Venkata Hemanjani Bhavana , Hillary K Graves , Sujay Kansagra , Joan M Jasien , Nicholas Stong , Boris Keren , Cyril Mignot , Claudia Ravelli , Auteur inconnu , Hugo J Bellen , Michael F Wangler , Vandana Shashi , Shinya Yamamoto

Missense variants in CTNNB1 can be associated with vitreoretinopathy-Seven new cases of CTNNB1-associated neurodevelopmental disorder including a previously unreported retinal phenotype.

Molecular genetics & genomic medicine
Avec: Linda Z Rossetti , Mir Reza Bekheirnia , Andrea M Lewis , Heather C Mefford , Katie Golden-Grant , Kristina Tarczy-Hornoch , Lauren C Briere , David A Sweetser , Melissa A Walker , Elijah Kravets , David A Stevenson , Georgette Bruenner , Jessica Sebastian , Julia Knapo , Jill A Rosenfeld , Paul C Marcogliese , Auteur inconnu , Michael F Wangler

Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Mengqi Ma , Mythily Ganapathi , Yiming Zheng , Kai-Li Tan , Oguz Kanca , Kevin E Bove , Norma Quintanilla , Sebnem O Sag , Sehime G Temel , Charles A LeDuc , Amanda J McPartland , Elaine M Pereira , Yufeng Shen , Jacob Hagen , Christie P Thomas , Nhu Thao Nguyen Galván , Xueyang Pan , Shenzhao Lu , Jill A Rosenfeld , Daniel G Calame , Michael F Wangler , James R Lupski , Davut Pehlivan , Paula M Hertel , Wendy K Chung , Hugo J Bellen

Novel hemizygous single-nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing loss.

Molecular genetics & genomic medicine
Avec: Ryan J German , Blake Vuocolo , Liesbeth Vossaert , Nichole Owen , Richard A Lewis , Lisa Saba , Auteur inconnu , Michael F Wangler , Sandesh Nagamani

Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.

Nature communications
Avec: Hui Guo , Elisa Bettella , Paul C Marcogliese , Rongjuan Zhao , Jonathan C Andrews , Tomasz J Nowakowski , Madelyn A Gillentine , Kendra Hoekzema , Tianyun Wang , Huidan Wu , Sharayu Jangam , Cenying Liu , Hailun Ni , Marjolein H Willemsen , Bregje W van Bon , Tuula Rinne , Servi J C Stevens , Tjitske Kleefstra , Han G Brunner , Helger G Yntema , Min Long , Wenjing Zhao , Zhengmao Hu , Cindy Colson , Nicolas Richard , Charles E Schwartz , Corrado Romano , Lucia Castiglia , Maria Bottitta , Shweta U Dhar , Deanna J Erwin , Lisa Emrick , Boris Keren , Alexandra Afenjar , Baosheng Zhu , Bing Bai , Pawel Stankiewicz , Kristin Herman , Auteur inconnu , Saadet Mercimek-Andrews , Jane Juusola , Amy B Wilfert , Rami Abou Jamra , Benjamin Büttner , Heather C Mefford , Alison M Muir , Ingrid E Scheffer , Brigid M Regan , Stephen Malone , Jozef Gecz , Jan Cobben , Marjan M Weiss , Quinten Waisfisz , Emilia K Bijlsma , Mariëtte J V Hoffer , Claudia A L Ruivenkamp , Stefano Sartori , Fan Xia , Jill A Rosenfeld , Raphael A Bernier , Michael F Wangler , Shinya Yamamoto , Kun Xia , Alexander P A Stegmann , Hugo J Bellen , Alessandra Murgia , Evan E Eichler

De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.

American journal of human genetics
Avec: Oguz Kanca , Jonathan C Andrews , Pei-Tseng Lee , Chirag Patel , Stephen R Braddock , Anne M Slavotinek , Julie S Cohen , Cynthia S Gubbels , Kimberly A Aldinger , Judy Williams , Maanasa Indaram , Ali Fatemi , Timothy W Yu , Pankaj B Agrawal , Gilbert Vezina , Cas Simons , Joanna Crawford , C Christopher Lau , Auteur inconnu , Wendy K Chung , Thomas C Markello , William B Dobyns , David R Adams , William A Gahl , Michael F Wangler , Shinya Yamamoto , Hugo J Bellen , May Christine V Malicdan

A Genocentric Approach to Discovery of Mendelian Disorders.

American journal of human genetics
Avec: Adam W Hansen , Mullai Murugan , He Li , Michael M Khayat , Liwen Wang , Jill Rosenfeld , B Kim Andrews , Shalini N Jhangiani , Zeynep H Coban Akdemir , Fritz J Sedlazeck , Allison E Ashley-Koch , Pengfei Liu , Donna M Muzny , Auteur inconnu , Erica E Davis , Nicholas Katsanis , Aniko Sabo , Jennifer E Posey , Yaping Yang , Michael F Wangler , Christine M Eng , V Reid Sutton , James R Lupski , Eric Boerwinkle , Richard A Gibbs

De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy.

American journal of human genetics
Avec: Hyung-Lok Chung , Xiao Mao , Hua Wang , Ye-Jin Park , Paul C Marcogliese , Jill A Rosenfeld , Lindsay C Burrage , Pengfei Liu , David R Murdock , Shinya Yamamoto , Michael F Wangler , Auteur inconnu , Hsiao-Tuan Chao , Hongyu Long , Li Feng , Carlos A Bacino , Hugo J Bellen , Bo Xiao

Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision.

Orphanet journal of rare diseases
Avec: Dustin Baldridge , Michael F Wangler , Angela N Bowman , Shinya Yamamoto , Auteur inconnu , Tim Schedl , Stephen C Pak , John H Postlethwait , Jimann Shin , Lilianna Solnica-Krezel , Hugo J Bellen , Monte Westerfield

Complex effects on Ca

Scientific reports
Avec: Benjamin J Grosso , Audra A Kramer , Sidharth Tyagi , Daniel F Bennett , Cynthia J Tifft , Precilla D'Souza , Michael F Wangler , Ellen F Macnamara , Ulises Meza , Roger A Bannister

A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins.

Cell reports
Avec: Annabel Guichard , Shenzhao Lu , Oguz Kanca , Daniel Bressan , Yan Huang , Mengqi Ma , Sara Sanz Juste , Jonathan C Andrews , Kristy L Jay , Marketta Sneider , Ruth Schwartz , Mei-Chu Huang , Danqing Bei , Hongling Pan , Liwen Ma , Wen-Wen Lin , Ankush Auradkar , Pranjali Bhagwat , Soo Park , Kenneth H Wan , Takashi Ohsako , Toshiyuki Takano-Shimizu , Susan E Celniker , Michael F Wangler , Shinya Yamamoto , Hugo J Bellen , Ethan Bier

Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies.

American journal of human genetics
Avec: Zelha Nil , Ashish R Deshwar , Yan Huang , Scott Barish , Xi Zhang , Sanaa Choufani , Polona Le Quesne Stabej , Ian Hayes , Patrick Yap , Chad Haldeman-Englert , Carolyn Wilson , Trine Prescott , Kristian Tveten , Arve Vøllo , Devon Haynes , Patricia G Wheeler , Jessica Zon , Cheryl Cytrynbaum , Rebekah Jobling , Moira Blyth , Siddharth Banka , Alexandra Afenjar , Cyril Mignot , Florence Robin-Renaldo , Boris Keren , Oguz Kanca , Xiao Mao , Daniel J Wegner , Kathleen Sisco , Marwan Shinawi , Auteur inconnu , Michael F Wangler , Rosanna Weksberg , Shinya Yamamoto , Gregory Costain , Hugo J Bellen

The fruit fly at the interface of diagnosis and pathogenic mechanisms of rare and common human diseases.

Human molecular genetics
Avec: Hugo J Bellen , Michael F Wangler , Shinya Yamamoto

Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Magdalena Koczkowska , Tom Callens , Alicia Gomes , Angela Sharp , Yunjia Chen , Alesha D Hicks , Arthur S Aylsworth , Amedeo A Azizi , Donald G Basel , Gary Bellus , Lynne M Bird , Maria A Blazo , Leah W Burke , Ashley Cannon , Felicity Collins , Colette DeFilippo , Ellen Denayer , Maria C Digilio , Shelley K Dills , Laura Dosa , Robert S Greenwood , Cristin Griffis , Punita Gupta , Rachel K Hachen , Concepción Hernández-Chico , Sandra Janssens , Kristi J Jones , Justin T Jordan , Peter Kannu , Bruce R Korf , Andrea M Lewis , Robert H Listernick , Fortunato Lonardo , Maurice J Mahoney , Mayra Martinez Ojeda , Marie T McDonald , Carey McDougall , Nancy Mendelsohn , David T Miller , Mari Mori , Rianne Oostenbrink , Sebastién Perreault , Mary Ella Pierpont , Carmelo Piscopo , Dinel A Pond , Linda M Randolph , Katherine A Rauen , Surya Rednam , S Lane Rutledge , Veronica Saletti , G Bradley Schaefer , Elizabeth K Schorry , Daryl A Scott , Andrea Shugar , Elizabeth Siqveland , Lois J Starr , Ashraf Syed , Pamela L Trapane , Nicole J Ullrich , Emily G Wakefield , Laurence E Walsh , Michael F Wangler , Elaine Zackai , Kathleen B M Claes , Katharina Wimmer , Rick van Minkelen , Alessandro De Luca , Yolanda Martin , Eric Legius , Ludwine M Messiaen

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.

Cell reports
Avec: Paul C Marcogliese , Samantha L Deal , Jonathan Andrews , J Michael Harnish , V Hemanjani Bhavana , Hillary K Graves , Sharayu Jangam , Xi Luo , Ning Liu , Danqing Bei , Yu-Hsin Chao , Brooke Hull , Pei-Tseng Lee , Hongling Pan , Pradnya Bhadane , Mei-Chu Huang , Colleen M Longley , Hsiao-Tuan Chao , Hyung-Lok Chung , Nele A Haelterman , Oguz Kanca , Sathiya N Manivannan , Linda Z Rossetti , Ryan J German , Amanda Gerard , Eva Maria Christina Schwaibold , Sarah Fehr , Renzo Guerrini , Annalisa Vetro , Eleina England , Chaya N Murali , Tahsin Stefan Barakat , Marieke F van Dooren , Martina Wilke , Marjon van Slegtenhorst , Gaetan Lesca , Isabelle Sabatier , Nicolas Chatron , Catherine A Brownstein , Jill A Madden , Pankaj B Agrawal , Boris Keren , Thomas Courtin , Laurence Perrin , Melanie Brugger , Timo Roser , Steffen Leiz , Frederic Tran Mau-Them , Julian Delanne , Elena Sukarova-Angelovska , Slavica Trajkova , Erik Rosenhahn , Vincent Strehlow , Konrad Platzer , Roberto Keller , Lisa Pavinato , Alfredo Brusco , Jill A Rosenfeld , Ronit Marom , Michael F Wangler , Shinya Yamamoto

Clinical diagnosis of metabolic disorders using untargeted metabolomic profiling and disease-specific networks learned from profiling data.

Scientific reports
Avec: Lillian R Thistlethwaite , Xiqi Li , Lindsay C Burrage , Kevin Riehle , Joseph G Hacia , Nancy Braverman , Michael F Wangler , Marcus J Miller , Sarah H Elsea , Aleksandar Milosavljevic

An Integrated Phenotypic and Genotypic Approach Reveals a High-Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger Domain.

Annals of neurology
Avec: Cole A Deisseroth , Vanesa C Lerma , Christina L Magyar , Jessica Mae Pfliger , Aarushi Nayak , Nathan D Bliss , Ashley W LeMaire , Vinodh Narayanan , Christopher Balak , Ginevra Zanni , Enza Maria Valente , Enrico Bertini , Paul J Benke , Michael F Wangler , Hsiao-Tuan Chao

The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder.

Human molecular genetics
Avec: Scott Barish , Mumine Senturk , Kelly Schoch , Amanda L Minogue , Diego Lopergolo , Chiara Fallerini , Jake Harland , Jacob H Seemann , Nicholas Stong , Peter G Kranz , Sujay Kansagra , Mohamad A Mikati , Joan Jasien , Mays El-Dairi , Paolo Galluzzi , Auteur inconnu , Francesca Ariani , Alessandra Renieri , Francesca Mari , Michael F Wangler , Swathi Arur , Yong-Hui Jiang , Shinya Yamamoto , Vandana Shashi , Hugo J Bellen

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Thomas A Ravenscroft , Jennifer B Phillips , Elizabeth Fieg , Sameer S Bajikar , Judy Peirce , Jeremy Wegner , Alia A Luna , Eric J Fox , Yi-Lin Yan , Jill A Rosenfeld , Jonathan Zirin , Oguz Kanca , Auteur inconnu , Paul J Benke , Eric S Cameron , Vincent Strehlow , Konrad Platzer , Rami Abou Jamra , Chiara Klöckner , Matthew Osmond , Thomas Licata , Samantha Rojas , David Dyment , Josephine S C Chong , Sharyn Lincoln , Joan M Stoler , John H Postlethwait , Michael F Wangler , Shinya Yamamoto , Joel Krier , Monte Westerfield , Hugo J Bellen

ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research.

Human mutation
Avec: J Michael Harnish , Lucian Li , Sanja Rogic , Guillaume Poirier-Morency , Seon-Young Kim , Auteur inconnu , Kym M Boycott , Michael F Wangler , Hugo J Bellen , Philip Hieter , Paul Pavlidis , Zhandong Liu , Shinya Yamamoto

Bi-allelic variants in INTS11 are associated with a complex neurological disorder.

American journal of human genetics
Avec: Burak Tepe , Erica L Macke , Marcello Niceta , Monika Weisz Hubshman , Oguz Kanca , Laura Schultz-Rogers , Yuri A Zarate , G Bradley Schaefer , Jorge Luis Granadillo De Luque , Daniel J Wegner , Benjamin Cogne , Brigitte Gilbert-Dussardier , Xavier Le Guillou , Eric J Wagner , Lynn S Pais , Jennifer E Neil , Ganeshwaran H Mochida , Christopher A Walsh , Nurit Magal , Valerie Drasinover , Mordechai Shohat , Tanya Schwab , Chris Schmitz , Karl Clark , Anthony Fine , Brendan Lanpher , Ralitza Gavrilova , Pierre Blanc , Lydie Burglen , Alexandra Afenjar , Dora Steel , Manju A Kurian , Prab Prabhakar , Sophie Gößwein , Nataliya Di Donato , Enrico S Bertini , Auteur inconnu , Michael F Wangler , Shinya Yamamoto , Marco Tartaglia , Eric W Klee , Hugo J Bellen

medRxiv : the preprint server for health sciences
Avec: Mengqi Ma , Yiming Zheng , Shenzhao Lu , Xueyang Pan , Kim C Worley , Lindsay C Burrage , Lauren S Blieden , Aimee Allworth , Wei-Liang Chen , Giuseppe Merla , Barbara Mandriani , Jill A Rosenfeld , David Li-Kroeger , Debdeep Dutta , Shinya Yamamoto , Michael F Wangler , Auteur inconnu , Ian A Glass , Sam Strohbehn , Elizabeth Blue , Paolo Prontera , Seema R Lalani , Hugo J Bellen

Réseau de co-auteurs

Shinya Yamamoto 20 collaborations
None None 18 collaborations
Hugo J Bellen 18 collaborations
Jill A Rosenfeld 10 collaborations
Oguz Kanca 10 collaborations
Paul C Marcogliese 6 collaborations
James R Lupski 5 collaborations
Pengfei Liu 5 collaborations
Jennifer E Posey 4 collaborations
Sharayu Jangam 4 collaborations
Lindsay C Burrage 4 collaborations
Hsiao-Tuan Chao 4 collaborations
Boris Keren 4 collaborations
Debdeep Dutta 3 collaborations
Zhandong Liu 3 collaborations
Hillary K Graves 3 collaborations
J Michael Harnish 3 collaborations
Mengqi Ma 3 collaborations
Shenzhao Lu 3 collaborations
Jonathan C Andrews 3 collaborations
Alexandra Afenjar 3 collaborations
Linyan Meng 2 collaborations
Frances A High 2 collaborations
Claudia Ravelli 2 collaborations
Lydie Burglen 2 collaborations
Daniel G Calame 2 collaborations
Davut Pehlivan 2 collaborations
Yaping Yang 2 collaborations
Pradnya Bhadane 2 collaborations
Marcus J Miller 2 collaborations
Lucian Li 2 collaborations
Christine M Eng 2 collaborations
Fan Xia 2 collaborations
Antonella Pignata 2 collaborations
Lauren C Briere 2 collaborations
Melissa A Walker 2 collaborations
Joel Krier 2 collaborations
Cas Simons 2 collaborations
David A Sweetser 2 collaborations
Ashley Cannon 2 collaborations
Shalini N Jhangiani 2 collaborations
Ronit Marom 2 collaborations
Samantha L Deal 2 collaborations
Michael M Khayat 2 collaborations
He Li 2 collaborations
Adam W Hansen 2 collaborations
Emilia K Bijlsma 2 collaborations
Claudia A L Ruivenkamp 2 collaborations
Richard A Gibbs 2 collaborations
Xi Luo 2 collaborations
Kelly Schoch 2 collaborations
Sujay Kansagra 2 collaborations
Nicholas Stong 2 collaborations
Cyril Mignot 2 collaborations
Vandana Shashi 2 collaborations
Linda Z Rossetti 2 collaborations
Andrea M Lewis 2 collaborations
Heather C Mefford 2 collaborations
Yiming Zheng 2 collaborations
Xueyang Pan 2 collaborations
Wendy K Chung 2 collaborations
Ryan J German 2 collaborations
Rami Abou Jamra 2 collaborations
Pei-Tseng Lee 2 collaborations
Pankaj B Agrawal 2 collaborations
Hyung-Lok Chung 2 collaborations
Xiao Mao 2 collaborations
John H Postlethwait 2 collaborations
Monte Westerfield 2 collaborations
Yan Huang 2 collaborations
Mei-Chu Huang 2 collaborations
Danqing Bei 2 collaborations
Hongling Pan 2 collaborations
Scott Barish 2 collaborations
Daniel J Wegner 2 collaborations
G Bradley Schaefer 2 collaborations
Vincent Strehlow 2 collaborations
Konrad Platzer 2 collaborations
Paul J Benke 2 collaborations
Joshua Manor 1 collaboration
Hyunglok Chung 1 collaboration
Pranjali K Bhagwat 1 collaboration
Rebecca Martinez-Moreno 1 collaboration
Elisabet Selga 1 collaboration
Helena Riuró 1 collaboration
David Carreras 1 collaboration
Mered Parnes 1 collaboration
Chandra Srinivasan 1 collaboration
Guillermo J Pérez 1 collaboration
Fabiana S Scornik 1 collaboration
Ramon Brugada 1 collaboration
Pirjo Isohanni 1 collaboration
Yunru Shao 1 collaboration
Brett H Graham 1 collaboration
Scott E Hickey 1 collaboration
Stephanie Brooks 1 collaboration
Anu Suomalainen 1 collaboration
Pascal Joset 1 collaboration
Katharina Steindl 1 collaboration
Anita Rauch 1 collaboration
Annette Hackenberg 1 collaboration
Amy Armstrong-Javors 1 collaboration
Niccolò E Mencacci 1 collaboration
Paulina Gonzàlez-Latapi 1 collaboration
Walaa A Kamel 1 collaboration
Jasem Y Al-Hashel 1 collaboration
Bernabé I Bustos 1 collaboration
Alejandro V Hernandez 1 collaboration
Dimitri Krainc 1 collaboration
Steven J Lubbe 1 collaboration
Hilde Van Esch 1 collaboration
Chiara De Luca 1 collaboration
Katleen Ballon 1 collaboration
Leila Qebibo 1 collaboration
Tadahiro Mitani 1 collaboration
Dana Marafi 1 collaboration
Nebal W Saadi 1 collaboration
Yavuz Sahin 1 collaboration
Reza Maroofian 1 collaboration
Stephanie Efthymiou 1 collaboration
Henry Houlden 1 collaboration
Shazia Maqbool 1 collaboration
Fatima Rahman 1 collaboration
Shen Gu 1 collaboration
Jill V Hunter 1 collaboration
Christopher J Carroll 1 collaboration
Saloni Sharma 1 collaboration
Brenna Hourigan 1 collaboration
Zain Patel 1 collaboration
Katie M Chan 1 collaboration
Joanna S Yi 1 collaboration
Anna Lehman 1 collaboration
Gabriella Horvath 1 collaboration
Paul A Cloos 1 collaboration
Qiumin Tan 1 collaboration
Rishi V Shridharan 1 collaboration
Benjamin Steger 1 collaboration
Marie Morimoto 1 collaboration
F Graeme Frost 1 collaboration
Ellen Macnamara 1 collaboration
Andreas Jenny 1 collaboration
David Adams 1 collaboration
May C Malicdan 1 collaboration
Barbara Lesko 1 collaboration
Rejwi Dahal 1 collaboration
Theodore E Wilson 1 collaboration
Molly McPheron 1 collaboration
Dongxue Mao 1 collaboration
Chaozhong Liu 1 collaboration
Linhua Wang 1 collaboration
Rami Ai-Ouran 1 collaboration
Cole Deisseroth 1 collaboration
Sasidhar Pasupuleti 1 collaboration
Seon Young Kim 1 collaboration
Michael Santana 1 collaboration
Victor Perez 1 collaboration
Priyank Shukla 1 collaboration
Brendan Lee 1 collaboration
Bo Yuan 1 collaboration
Jidong Liu 1 collaboration
Guolian Ding 1 collaboration
Kexin Zou 1 collaboration
Ziru Jiang 1 collaboration
Junyu Zhang 1 collaboration
Yunhua Lu 1 collaboration
Eric Venner 1 collaboration
Zheng Sun 1 collaboration
Adeline Vanderver 1 collaboration
Nikkola Carmichael 1 collaboration
Christine Callahan 1 collaboration
Ryan J Taft 1 collaboration
Guy Helman 1 collaboration
Undiagnosed Diseases Network 1 collaboration
Katharina V Schulze 1 collaboration
Neil A Hanchard 1 collaboration
Kai Li Tan 1 collaboration
Elaine S Seto 1 collaboration
Nurit Assia Batzir 1 collaboration
Pranjali Kishor Bhagwat 1 collaboration
Austin Larson 1 collaboration
Zeynep Coban Akdemir 1 collaboration
Maciej Bagłaj 1 collaboration
Leon Bofferding 1 collaboration
Katherine B Bosanko 1 collaboration
Skander Bouassida 1 collaboration
Bert Callewaert 1 collaboration
Yazmin Enchautegui Colon 1 collaboration
Adolfo D Garnica 1 collaboration
Margaret H Harr 1 collaboration
Sandra Heck 1 collaboration
Anna C E Hurst 1 collaboration
Bertrand Isidor 1 collaboration
Rebecca O Littlejohn 1 collaboration
Pilar Magoulas 1 collaboration
Helen Mar Fan 1 collaboration
Scott McLean 1 collaboration
Marjan M Nezarati 1 collaboration
Kimberly M Nugent 1 collaboration
Michael B Petersen 1 collaboration
Maria L Rocha 1 collaboration
Elizabeth Roeder 1 collaboration
Robert Smigiel 1 collaboration
Ian Tully 1 collaboration
James Weisfeld-Adams 1 collaboration
Katerina O Wells 1 collaboration
Arthur L Beaudet 1 collaboration
Jianhong Hu 1 collaboration
Yunyun Jiang 1 collaboration
Varuna Chander 1 collaboration
Moez Dawood 1 collaboration
Shoudong Li 1 collaboration
Jennifer Friedman 1 collaboration
Laura Cross 1 collaboration
Francis H Sansbury 1 collaboration
Jeffrey W Innis 1 collaboration
Jessica Omark O'Shea 1 collaboration
Qingchang Meng 1 collaboration
Kirsty McWalter 1 collaboration
David Murdock 1 collaboration
Sharayu V Jangam 1 collaboration
Venkata Hemanjani Bhavana 1 collaboration
Joan M Jasien 1 collaboration
Mir Reza Bekheirnia 1 collaboration
Katie Golden-Grant 1 collaboration
Kristina Tarczy-Hornoch 1 collaboration
Elijah Kravets 1 collaboration
David A Stevenson 1 collaboration
Georgette Bruenner 1 collaboration
Jessica Sebastian 1 collaboration
Julia Knapo 1 collaboration
Mythily Ganapathi 1 collaboration
Kai-Li Tan 1 collaboration
Kevin E Bove 1 collaboration
Norma Quintanilla 1 collaboration
Sebnem O Sag 1 collaboration
Sehime G Temel 1 collaboration
Charles A LeDuc 1 collaboration
Amanda J McPartland 1 collaboration
Elaine M Pereira 1 collaboration
Yufeng Shen 1 collaboration
Jacob Hagen 1 collaboration
Christie P Thomas 1 collaboration
Nhu Thao Nguyen Galván 1 collaboration
Paula M Hertel 1 collaboration
Blake Vuocolo 1 collaboration
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