Paul S Kruszka (Paul Kruszka)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 42

Top Venues

American journal of medical genetics. Part C, Seminars in medical genetics

American journal of medical genetics. Part A

bioRxiv : the preprint server for biology

Birth defects research

National Institutes of Health

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Institutes of Health Jul 01 2011

United States

Clinical Geneticist :: National Human Genome Research Institute

Publications

Maria Carla Borroto, Coralie Michaud, Chloé Hudon, Pankaj B Agrawal, Katherine Agre, Carolyn D Applegate, Alan H Beggs, Hans T Bjornsson, Bert Callewaert, Mei-Jan Chen, Cynthia Curry, Orrin Devinsky, Tracy Dudding-Byth, Kelly Fagan, Candice R Finnila, Ralitza Gavrilova, Casie A Genetti, Susan M Hiatt, Friedhelm Hildebrandt, Monica Hsiung Wojcik, Tjitske Kleefstra, Caroline M Kolvenbach, Bruce R Korf, Paul S Kruszka, Hong Li, Jessica Litwin, Julien Marcadier, Konrad Platzer, Patrick R Blackburn, Margot R F Reijnders, Heiko Martin Reutter, Ina Schanze, Joseph T Shieh, Cathy A Stevens, Zaheer Valivullah, Marie-José H van den Boogaard, Eric W Klee, Philippe M Campeau
A Genotype/Phenotype Study of KDM5B -Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense Variants. Genes 15 (8) (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Maria Carla Borroto, Coralie Michaud, Chloé Hudon, Pankaj B Agrawal, Katherine Agre, Carolyn D Applegate, Alan H Beggs, Hans T Bjornsson, Bert Callewaert, Mei-Jan Chen, Cynthia Curry, Orrin Devinsky, Tracy Dudding-Byth, Kelly Fagan, Candice R Finnila, Ralitza Gavrilova, Casie A Genetti, Susan M Hiatt, Friedhelm Hildebrandt, Monica Hsiung Wojcik, Tjitske Kleefstra, Caroline M Kolvenbach, Bruce R Korf, Paul S Kruszka, Hong Li, Jessica Litwin, Julien Marcadier, Konrad Platzer, Patrick R Blackburn, Margot R F Reijnders, Heiko Martin Reutter, Ina Schanze, Joseph T Shieh, Cathy A Stevens, Zaheer Valivullah, Marie-José H van den Boogaard, Eric W Klee, Philippe M Campeau
A Genotype/Phenotype Study of KDM5B -Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense Variants. Genes 15 (8) (2024)
Elizabeth I Pierpont, Anton M Bennett, Lisa Schoyer, Beth Stronach, April Anschutz, Sarah C Borrie, Benjamin Briggs, Emma Burkitt-Wright, Pau Castel, Ion C Cirstea, Fieke Draaisma, Michelle Ellis, Vanessa S Fear, Megan N Frone, Elisabetta Flex, Bruce D Gelb, Tamar Green, Karen W Gripp, Sattar Khoshkhoo, Mark W Kieran, Karolin Kleemann, Bonita P Klein-Tasman, Maria I Kontaridis, Paul S Kruszka, Chiara Leoni, Clifford Z Liu, Nadia Merchant, Pilar L Magoulas, Christopher Moertel, Carlos E Prada, Katherine A Rauen, Renée Roelofs, Rodrigue Rossignol, Christine Sevilla, Gigi Sevilla, Ryan Sheedy, Elliot Stieglitz, Daochun Sun, Dagmar Tiemens, Forest White, Ellen Wingbermühle, Cordula Wolf, Martin Zenker, Gregor Andelfinger
The 8th International RASopathies Symposium: Expanding research and care practice through global collaboration and advocacy. American journal of medical genetics. Part A (2023)
Ekanem N Ekure, Kareem O Musa, Ngozi Ulonnam, Paul S Kruszka, Maximilian Muenke, Adebowale A Adeyemo
Ambiguous genitalia, giant congenital melanocytic nevus and subpulmonic outlet ventricular septal defect in an African child with Neurofibromatosis 1. American journal of medical genetics. Part A (2023)
Adrianna K San Roman, Helen Skaletsky, Alexander K Godfrey, Neha V Bokil, Levi Teitz, Isani Singh, Laura V Blanton, Daniel W Bellott, Tatyana Pyntikova, Julian Lange, Natalia Koutseva, Jennifer F Hughes, Laura Brown, Sidaly Phou, Ashley Buscetta, Paul S Kruszka, Nicole Banks, Amalia Dutra, Evgenia Pak, Patricia C Lasutschinkow, Colleen Keen, Shanlee M Davis, Angela E Lin, Nicole R Tartaglia, Carole A Samango-Sprouse, Maximilian Muenke, David C Page
The human Y and inactive X chromosomes similarly modulate autosomal gene expression. bioRxiv : the preprint server for biology (2023)
Ekanem N Ekure, Ogochukwu Sokunbi, Paul S Kruszka, Maximilian Muenke, Adebowale A Adeyemo
Hajdu-Cheney syndrome with atypical cardiovascular abnormalities. American journal of medical genetics. Part A (2022)
Maegan E Roberts, Sarah Nimrichter, Megan L Marshall, Elizabeth K Flynn, Rick Person, Kathleen S Hruska, Paul S Kruszka, Jane Juusola
Phenotypic continuum between POLE-related recessive disorders: A case report and literature review. American journal of medical genetics. Part A 188 (10) (2022)
Cedrik Tekendo-Ngongang, Paul S Kruszka
Noonan syndrome on the African Continent. Birth defects research 112 (10) (2021)
Joe Brough, Mahim Jain, Teodoro Jerves, Paul S Kruszka, Elizabeth McGuffey
Genetic screening for hypertrophic cardiomyopathy in large, asymptomatic military cohorts. American journal of medical genetics. Part C, Seminars in medical genetics 184 (1) (2020)
Paul S Kruszka, Andrea Zawacki Beaton
The state of congenital heart disease. American journal of medical genetics. Part C, Seminars in medical genetics 184 (1) (2020)
Cedrik Tekendo-Ngongang, Babajide Owosela, Maximilian Muenke, Paul S Kruszka
Comorbidity of congenital heart defects and holoprosencephaly is likely genetically driven and gene-specific. American journal of medical genetics. Part C, Seminars in medical genetics 184 (1) (2020)
Yonit A Addissie, Paul S Kruszka, Angela Troia, Zoë C Wong, Joshua L Everson, Beth A Kozel, Robert J Lipinski, Kristen M C Malecki, Maximilian Muenke
Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study. Environmental health : a global access science source 19 (1) (2020)
Sarthak Gupta, Shuichiro Nakabo, Luz P Blanco, Liam J O'Neil, Gustaf Wigerblad, Rishi Raj Goel, Pragnesh Mistry, Kan Jiang, Carmelo Carmona-Rivera, Diana W Chan, Xinghao Wang, Hege Lynum Pedersen, Manasi Gadkari, Katherine N Howe, Faiza Naz, Stefania Dell'Orso, Sarfaraz A Hasni, Caeden Dempsey, Ashley Buscetta, Pamela A Frischmeyer-Guerrerio, Paul S Kruszka, Maximilian Muenke, Luis Miguel Franco, Hong-Wei Sun, Mariana J Kaplan
Sex differences in neutrophil biology modulate response to type I interferons and immunometabolism. Proceedings of the National Academy of Sciences of the United States of America 117 (28) (2020)
Ekanem N Ekure, Ogochukwu J Sokunbi, Nnenna Kalu, Akinsanya Olusegun-Joseph, Oyewole Kushimo, Casmir Amadi, Olayinka Hassan, Desmond Ikebudu, Sophia Onyia, Chinonso Onwudiwe, Victor Nwankwo, Remi Akinwunmi, Fukpode Awusa, Zainab Akere, Olaolu Dele-Salawu, Elizabeth Ajayi, Olagoke Ale, Dorothy Muoneke, Maximillian Muenke, Paul S Kruszka, Andrea Zawacki Beaton, Craig A Sable, Adebowale Adeyemo
Congenital heart disease in school children in Lagos, Nigeria: Prevalence and the diagnostic gap. American journal of medical genetics. Part C, Seminars in medical genetics 184 (1) (2020)
Cedrik Tekendo-Ngongang, Babajide Owosela, Nicole Fleischer, Yonit A Addissie, Bryan Malonga, Ebenezer Badoe, Neerja Gupta, Angélica Moresco, Victoria Huckstadt, Engy A Ashaat, Dalia Farouk Hussen, Ho-Ming Luk, Ivan F M Lo, Brian Hon-Yin Chung, Jasmine L F Fung, Danilo Moretti-Ferreira, Letícia Cassimiro Batista, Stephanie Lotz-Esquivel, Manuel Saborio-Rocafort, Ramses Badilla-Porras, Monica Penon-Portmann, Kelly L Jones, Omar A Abdul-Rahman, Annette Uwineza, Eloise J Prijoles, Ifeanyi Kanayo Ifeorah, Arianne Llamos Paneque, Nirmala D Sirisena, Leah Ke'ala'aumoe Dowsett, Sansan Lee, Gerarda Cappuccio, Carolyn Sian Kitchin, Alicia Diaz-Kuan, Meow-Keong Thong, María Gabriela Obregon, Leon Mutesa, Vajira H W Dissanayake, Mona O El Ruby, Nicola Brunetti-Pierri, Ekanem Nsikak Ekure, Roger E Stevenson, Maximilian Muenke, Paul S Kruszka
Rubinstein-Taybi syndrome in diverse populations. American journal of medical genetics. Part A 182 (12) (2020)
Yonit A Addissie, Angela Troia, Zoe C Wong, Joshua L Everson, Beth A Kozel, Maximilian Muenke, Robert J Lipinski, Kristen M C Malecki, Paul S Kruszka
Identifying environmental risk factors and gene-environment interactions in holoprosencephaly. Birth defects research 113 (1) (2020)
Cedrik Tekendo-Ngongang, Paul S Kruszka, Ariel F Martinez, Maximilian Muenke
Novel heterozygous variants in KMT2D associated with holoprosencephaly. Clinical genetics 96 (3) (2019)
Leah Ke'ala'aumoe Dowsett, Antonio R Porras, Paul S Kruszka, Brandon Davis, Tommy Hu, Engela Honey, Eben Badoe, Meow-Keong Thong, Eyby Leon, Katta Mohan Girisha, Anju Shukla, Shalini S Nayak, Vorasuk Shotelersuk, Andre Megarbane, Shubha Rao Phadke, Nirmala D Sirisena, Vajira H W Dissanayake, Carlos R Ferreira, Monisha S Kisling, Pranoot Tanpaiboon, Annette Uwineza, Leon Mutesa, Cedrik Tekendo-Ngongang, Ambroise Wonkam, Karen Fieggen, Leticia Cassimiro Batista, Danilo Moretti-Ferreira, Roger E Stevenson, Eloise J Prijoles, David B Everman, Kate Clarkson, Jessica Worthington, Virginia E Kimonis, Fuki Hisama, Carol Crowe, Paul Wong, Kisha Johnson, Robin D Clark, Lynne Bird, Diane Masser-Frye, Marie McDonald, Patrick Willems, Elizabeth Roeder, Sulgana Saitta, Kwame Anyane-Yeoba, Laurie Demmer, Naoki Hamajima, Zornitza Stark, Greta Gillies, Louanne Hudgins, Usha Dave, Stavit Shalev, Victoria Siu, Ann Ades, Holly Dubbs, Sarah Raible, Maninder Kaur, Emanuela Salzano, Laird Jackson, Matthew Deardorff, Antonie D Kline, Marshall Summar, Maximilian Muenke, Marius George Linguraru, Ian D Krantz
Cornelia de Lange syndrome in diverse populations. American journal of medical genetics. Part A 179 (2) (2019)
Donald W Hadley, Paul S Kruszka, Maximilian Muenke
Challenging issues arising in counseling families experiencing holoprosencephaly. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2019)
Paul S Kruszka, Benjamin D Solomon, Maximilian Muenke
Introduction. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2019)
Paul S Kruszka, Tommy Hu, Sungkook Hong, Rebecca Signer, Benjamin Cogné, Betrand Isidor, Sarah E Mazzola, Jacques C Giltay, Koen L I van Gassen, Eleina M England, Lynn Pais, Charlotte W Ockeloen, Pedro A Sanchez-Lara, Esther Kinning, Darius J Adams, Kayla Treat, Wilfredo Torres-Martinez, Maria Francesca Bedeschi, Maria Iascone, Stephanie Blaney, Oliver Bell, Tiong Y Tan, Marie-Ange Delrue, Julie Jurgens, Brenda J Barry, Elizabeth C Engle, Sarah K Savage, Nicole Fleischer, Julian A Martinez, Kym M Boycott, Elaine H Zackai, Maximilian Muenke
Phenotype delineation of ZNF462 related syndrome. American journal of medical genetics. Part A 179 (10) (2019)
Teodoro Jerves, Andrea Zawacki Beaton, Paul S Kruszka
The genetic workup for structural congenital heart disease. American journal of medical genetics. Part C, Seminars in medical genetics 184 (1) (2019)
Ekanem N Ekure, Yonit A Addissie, Ogochukwu Jidechukwu Sokunbi, Paul S Kruszka, Maximilian Muenke, Adebowale A Adeyemo
Tuberous sclerosis in a patient from Nigeria. American journal of medical genetics. Part A 179 (8) (2019)
Benjamin D Solomon, Paul S Kruszka, Maximilian Muenke
Holoprosencephaly flashcards: An updated summary for the clinician. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2019)
Tommy Hu, Paul S Kruszka, Ariel F Martinez, Jeffrey E Ming, Emily K Shabason, Manu S Raam, Tamim H Shaikh, Daniel E Pineda-Alvarez, Maximilian Muenke
Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2019)
Paul S Kruszka, Michael Silberbach
The state of Turner syndrome science: Are we on the threshold of discovery? American journal of medical genetics. Part C, Seminars in medical genetics 181 (1) (2019)
Paul S Kruszka, Antonio R Porras, Deise Helena de Souza, Angélica Moresco, Victoria Huckstadt, Ashleigh D Gill, Alec P Boyle, Tommy Hu, Yonit A Addissie, Gary T K Mok, Cedrik Tekendo-Ngongang, Karen Fieggen, Eloise J Prijoles, Pranoot Tanpaiboon, Engela Honey, Ho-Ming Luk, Ivan F M Lo, Meow-Keong Thong, Premala Muthukumarasamy, Kelly L Jones, Khadija Belhassan, Karim Ouldim, Ihssane El Bouchikhi, Laila Bouguenouch, Anju Shukla, Katta Mohan Girisha, Nirmala D Sirisena, Vajira H W Dissanayake, C Sampath Paththinige, Rupesh Mishra, Monisha S Kisling, Carlos R Ferreira, María Beatriz de Herreros, Ni-Chung Lee, Saumya S Jamuar, Angeline Lai, Ee Shien Tan, Jiin Ying Lim, Cham Breana Wen-Min, Neerja Gupta, Stephanie Lotz-Esquivel, Ramsés Badilla-Porras, Dalia Farouk Hussen, Mona O El Ruby, Engy A Ashaat, Siddaramappa Jagdish Patil, Leah Dowsett, Alison Eaton, A Micheil Innes, Vorasuk Shotelersuk, Ëben Badoe, Ambroise Wonkam, María Gabriela Obregon, Brian H Y Chung, Milana Trubnykova, Jorge La Serna, Bertha Elena Gallardo Jugo, Miguel Chávez Pastor, Hugo Hernán Abarca Barriga, Andre Megarbane, Beth A Kozel, Mieke M van Haelst, Roger E Stevenson, Marshall Summar, A Adebowale Adeyemo, Colleen A Morris, Danilo Moretti-Ferreira, Marius George Linguraru, Maximilian Muenke
Williams-Beuren syndrome in diverse populations. American journal of medical genetics. Part A 176 (5) (2019)
Paul S Kruszka, Ashley Buscetta, Maria T Acosta, Nicole Banks, Yonit A Addissie, Camilo Toro, Marie Luby, Lawrence Latour, Gilbert Vezina, David C Page, Maximilian Muenke
Circle of Willis anomalies in Turner syndrome: Absent A1 segment of the anterior cerebral artery. Birth defects research 111 (19) (2019)
Karin Weiss, Paul S Kruszka, Eric Levey, Max Muenke
Holoprosencephaly from conception to adulthood. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2019)
Siddharth K Prakash, Soniely Lugo-Ruiz, Michelle Rivera-Dávila, Nunilo Rubio, Avni N Shah, Rebecca C Knickmeyer, Cindy Scurlock, Melissa Crenshaw, Shanlee M Davis, Gary A Lorigan, Aaron T Dorfman, Karen Rubin, Cheryl L Maslen, Vaneeta Bamba, Paul S Kruszka, Michael Silberbach, null null
The Turner syndrome research registry: Creating equipoise between investigators and participants. American journal of medical genetics. Part C, Seminars in medical genetics 181 (1) (2019)
Paul S Kruszka, Yonit A Addissie, Cedrik Tekendo-Ngongang, Kelly L Jones, Sarah K Savage, Neerja Gupta, Nirmala D Sirisena, Vajira H W Dissanayake, C Sampath Paththinige, Teresa Aravena, Sheela Nampoothiri, Dhanya Yesodharan, Katta Mohan Girisha, Siddaramappa Jagdish Patil, Saumya Shekhar Jamuar, Jasmine Chew-Yin Goh, Agustini Utari, Nydia Sihombing, Rupesh Mishra, Neer Shoba Chitrakar, Brenda C Iriele, Ezana Lulseged, Andre Megarbane, Annette Uwineza, Elizabeth Eberechi Oyenusi, Oluwarotimi Bolaji Olopade, Olufemi Adetola Fasanmade, Milagros M Duenas-Roque, Meow-Keong Thong, Joanna Y L Tung, Gary T K Mok, Nicole Fleischer, Godfrey M Rwegerera, María Beatriz de Herreros, Johnathan Watts, Karen Fieggen, Victoria Huckstadt, Angélica Moresco, María Gabriela Obregon, Dalia Farouk Hussen, Neveen A Ashaat, Engy A Ashaat, Brian H Y Chung, Eben Badoe, Sultana M H Faradz, Mona O El Ruby, Vorasuk Shotelersuk, Ambroise Wonkam, Ekanem Nsikak Ekure, Shubha Rao Phadke, Antonio Richieri-Costa, Maximilian Muenke
Turner syndrome in diverse populations. American journal of medical genetics. Part A 182 (2) (2019)
Paul S Kruszka, Ariel F Martinez, Maximilian Muenke
Molecular testing in holoprosencephaly. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2018)
Yu Abe, Paul S Kruszka, Ariel F Martinez, Erich Roessler, Kohei Shiota, Shigehito Yamada, Maximilian Muenke
Clinical and Demographic Evaluation of a Holoprosencephaly Cohort From the Kyoto Collection of Human Embryos. Anatomical record (Hoboken, N.J. : 2007) 301 (6) (2018)
Ariel F Martinez, Paul S Kruszka, Maximilian Muenke
Extracephalic manifestations of nonchromosomal, nonsyndromic holoprosencephaly. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2018)
Paul S Kruszka, Maximilian Muenke
Syndromes associated with holoprosencephaly. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2018)
Paul S Kruszka, Yonit A Addissie, Daniel E McGinn, Antonio R Porras, Elijah Biggs, Matthew Share, T Blaine Crowley, Brian H Y Chung, Gary T K Mok, Christopher C Y Mak, Premala Muthukumarasamy, Meow-Keong Thong, Nirmala D Sirisena, Vajira H W Dissanayake, C Sampath Paththinige, L B Lahiru Prabodha, Rupesh Mishra, Vorasuk Shotelersuk, Ekanem Nsikak Ekure, Ogochukwu Jidechukwu Sokunbi, Nnenna Kalu, Carlos R Ferreira, Jordann-Mishael Duncan, Siddaramappa Jagdish Patil, Kelly L Jones, Julie D Kaplan, Omar A Abdul-Rahman, Annette Uwineza, Leon Mutesa, Angélica Moresco, María Gabriela Obregon, Antonio Richieri-Costa, Vera L Gil-da-Silva-Lopes, Adebowale A Adeyemo, Marshall Summar, Elaine H Zackai, Donna M McDonald-McGinn, Marius George Linguraru, Maximilian Muenke
22q11.2 deletion syndrome in diverse populations. American journal of medical genetics. Part A 173 (4) (2017)
Paul S Kruszka, Antonio R Porras, Yonit A Addissie, Angélica Moresco, Sofia Medrano, Gary T K Mok, Gordon K C Leung, Cedrik Tekendo-Ngongang, Annette Uwineza, Meow-Keong Thong, Premala Muthukumarasamy, Engela Honey, Ekanem N Ekure, Ogochukwu J Sokunbi, Nnenna Kalu, Kelly L Jones, Julie D Kaplan, Omar A Abdul-Rahman, Lisa M Vincent, Amber Love, Khadija Belhassan, Karim Ouldim, Ihssane El Bouchikhi, Anju Shukla, Katta M Girisha, Siddaramappa Jagdish Patil, Nirmala D Sirisena, Vajira H W Dissanayake, C Sampath Paththinige, Rupesh Mishra, Eva Klein-Zighelboim, Bertha E Gallardo Jugo, Miguel Chávez Pastor, Hugo Hernán Abarca Barriga, Steven A Skinner, Eloise J Prijoles, Eben Badoe, Ashleigh D Gill, Vorasuk Shotelersuk, Patroula Smpokou, Monisha S Kisling, Carlos R Ferreira, Leon Mutesa, Andre Megarbane, Antonie D Kline, Amy Kimball, Emmy Okello, Peter Lwabi, Twalib Aliku, Emmanuel Tenywa, Nonglak Boonchooduang, Pranoot Tanpaiboon, Antonio Richieri-Costa, Ambroise Wonkam, Brian H Y Chung, Roger E Stevenson, Marshall Summar, Kausik Mandal, Shubha R Phadke, María G Obregon, Marius G Linguraru, Maximilian Muenke
Noonan syndrome in diverse populations. American journal of medical genetics. Part A 173 (9) (2017)
Bethany Stokes, Seth I Berger, Beth A Hall, Karin Weiss, Ariel F Martinez, Donald W Hadley, David R Murdock, Subhadra Ramanathan, Robin D Clark, Erich Roessler, Paul S Kruszka, Maximilian Muenke
SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly. Congenital anomalies 58 (1) (2017)

Paul S Kruszka.css-eqlu8i{font-size:small;padding-left:4px;} (Paul Kruszka)

Publication Activity (10 Years)

Top Topics

Top Venues

Paul S Kruszka (Paul Kruszka)