Millan S. Patel

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Research Interests:

Application of the Translational Care model to deliver care-focused research results more rapidly. Application of high throughput technologies such as genomics, metagenomics and other platform biology approaches to find molecular entry points to study a variety of rare diseases. Areas of interest include bone biology, preterm birth and eye diseases.

Research Interests

Papers共 100 篇Author StatisticsCo-AuthorSimilar Experts

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Missense Variants in Homeobox Domain of PBX1 Cause Coracoclavicular Ankylosis

Kenji Kurosawa, Maki Iwai,Kyra Stuurman, Kirsten Meagher,Lise Leveille,Takashi Saisu,Satomi Mori,Tatsuro Kumaki,Yumi Enomoto,Noriko Aida,Hisato Suzuki,Toshiki Takenouchi,Kenjiro Kosaki,Millan Patel,Gen Nishimura

crossref（2024）

Cited0Views0Bibtex

The Practice of Genomic Medicine: A Delineation of the Process and Its Governing Principles

Julia Handra,Adrienne Elbert,Nour Gazzaz,Ashley Moller-Hansen,Stephanie Hyunh,Hyun Kyung Lee,Pierre Boerkoel,Emily Alderman, Erin Anderson,Lorne Clarke,Sara Hamilton, Ronnalea Hamman, Shevaun Hughes, Simon Ip,Sylvie Langlois, Mary Lee, Laura Li, Frannie Mackenzie,Millan S. S. Patel, Leah M. M. Prentice,Karan Sangha, Laura Sato,Kimberly Seath,Margaret Seppelt,Anne Swenerton,Lynn Warnock,Jessica L. Zambonin,Cornelius F. Boerkoel,Hui-Lin Chin,Linlea Armstrong

FRONTIERS IN MEDICINE（2023）

Cited1Views0WOSBibtex

NOTCH1 Loss of the TAD and PEST Domain: an Antimorph

Pierre Boerkoel,Stephanie Huynh,Gui Xiang Yang,Cornelius F. F. Boerkoel,Millan S. S. Patel,Anna Lehman,Jefferson Terry,Adrienne Elbert

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 6 (2023): 1593-1598

Cited1Views0WOSBibtex

PP01.77 EMERGE 402: Real-world Characteristics and Safety of Lurbinectedin in Small-cell Lung Cancer (SCLC)

D. Schreeder,F. Badin,S. Dakhil,P. Lammers,M. Patel,D. Slater,J. Migas,N. Naveh,A. Boccuti,R. Hanvesakul,W. Li,B. Halmos

Journal of Thoracic Oncologyno. 3 (2023): e43-e43

Cited0Views0Bibtex

Impact of Variation in Practice in the Prenatal Reporting of Variants of Uncertain Significance by Commercial Laboratories: Need for Greater Adherence to Published Guidelines

Melissa Cornthwaite,Kelly Turner,Linlea Armstrong,Cornelius F. Boerkoel,Caitlin Chang,Anna Lehman,Sarah M. Nikkel,Millan S. Patel,Margot van Allen,Sylvie Langlois

OBSTETRICAL & GYNECOLOGICAL SURVEY（2023）

Cited1Views0Bibtex

Comprehensive Human Amniotic Fluid Metagenomics Supports the Sterile Womb Hypothesis

HanChen Wang,Gui Xiang Yang,Yuxiang Hu,Patricia Lam,Karan Sangha,Dawn Siciliano,Anne Swenerton,Ruth Miller,Peter Tilley,Peter Von Dadelszen,Shirin Kalyan,Patrick Tang,Millan S. Patel

Scientific Reports（2022）

Cited16Views0WOSNATUREBibtex

Genome-wide Sequencing and the Clinical Diagnosis of Genetic Disease: the CAUSES Study

Alison M. Elliott,Shelin Adam,Christele du Souich,Anna Lehman,Tanya N. Nelson,Clara van Karnebeek,Emily Alderman,Linlea Armstrong, Gudrun Aubertin,Katherine Blood,Cyrus Boelman,Cornelius Boerkoel, Karla Bretherick,Lindsay Brown,Chieko Chijiwa,Lorne Clarke,Madeline Couse,Susan Creighton, Abby Watts-Dickens,William T. Gibson,Harinder Gill,Maja Tarailo-Graovac,Sara Hamilton, Harindar Heran,Gabriella Horvath,Lijia Huang,Gurdip K. Hulait, David Koehn,Hyun Kyung Lee, Suzanne Lewis,Elena Lopez,Kristal Louie,Karen Niederhoffer,Allison Matthews, Kirsten Meagher,Junran J. Peng,Millan S. Patel,Simone Race,Phillip Richmond,Rosemarie Rupps,Ramona Salvarinova,Kimberly Seath,Kathryn Selby,Michelle Steinraths,Sylvia Stockler, Kaoru Tang,Christine Tyson,Margot van Allen,Wyeth Wasserman,Jill Mwenifumbo,Jan M. Friedman

Human Genetics and Genomics Advancesno. 3 (2022): 100108-100108

Cited14Views0WOSBibtex

Impact of Variation in Practice in the Prenatal Reporting of Variants of Uncertain Significance by Commercial Laboratories: Need for Greater Adherence to Published Guidelines

Melissa Cornthwaite,Kelly Turner,Linlea Armstrong,Cornelius F. Boerkoel,Caitlin Chang,Anna Lehman,Sarah M. Nikkel,Millan S. Patel,Margot Van Allen,Sylvie Langlois

Prenatal Diagnosis（2022）

Cited8Views0WOSBibtex

PIGG variant pathogenicity assessment reveals novel features within nineteen families

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

Cited0Views0Bibtex

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Clinical Professor

Papers共 100 篇Author StatisticsCo-AuthorSimilar Experts